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The flies of Saint Narcís and other animals (and plants, and bacteria) in Girona

Posted by , on 28 November 2016

In October I travelled to Girona, an old Catalan city surrounded by wooded hills a hundred kilometres north of Barcelona, for the 11th meeting of the Spanish Society for Developmental Biology (SEBD). The meeting was jointly organised with the SEBD’s neighbours, the Portuguese Society for Developmental Biology, and also the Spanish Society for Cell Biology, and thus gave me a broad overview of what’s currently going on in Iberian cell and developmental biology. I had been in Girona before, but only briefly and half a life ago, and took the chance to get to know the city at a time of year when it wasn’t swamped by tourists trying to find where the Game of Thrones scenes were shot.

 

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A view from the old town’s walls

 

I also had the chance to meet some wonderful welcoming people. I don’t want to get too hung up on the financial situation in Spanish research, but it popped up again and again in conversations between talks, over beers, at breakfast. (Brexit did provide an alternate but equally downbeat conversation topic!) That there is not enough money in Spanish research is clear – public investment in research has dropped dramatically since the financial crisis began, and is well below the European average. The funding systems themselves appear to be outdated, and there is a feeling that the current government is more interested in creating a service economy than one driven by research and innovation (“more beaches and casinos than labs and fellowships,” to paraphrase one senior researcher). In this environment, new PIs are in a particularly vulnerable state, and those I talked to didn’t see the situation changing anytime soon, as recounted elsewhere.

But, against this background, there is still fantastic research being carried out in Spanish labs, and there are still Spanish researchers returning home to establish their labs after postdocs abroad (plus foreign-born researchers working in and running Spanish labs). So let’s forget about money for a moment and move on to science!

 

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I began with a workshop organised by Xavier Trepat and María Garcia-Parajo on cell dynamics and nanobiology. The workshop aimed to highlight the new techniques that are revealing the dynamics of life at higher and higher resolution, and allowing us to measure forces and determine physical properties of tissues such as stiffness.

Jacky Goetz kicked off with a description of how multiple imaging modalities were helping his lab understand metastasis, and went through the painful-sounding process of combining intraviral imaging, micro CT and EM1 (we previously heard about CLEM approaches in an interview featuring Jacky’s collaborator Yannick Schwab). María Garcia-Parajo then took us on a tour of the plasma membrane at the nanoscale, before Jérome Solon zoomed out to the level of the tissue. Embryogenesis strikes him as origami, a single sheet folded into a complex three dimensional structure, except there is no origamist, and the properties of the material change as you progress. Defining forces is one thing, but Solon stressed that we should not forget the tissue’s response to these forces, which is heavily influenced by the cytoskeleton and the membrane. Xavier Trepat then finished with his lab’s recent work on durotaxis – the process by which cells follow gradients in substrate stiffness – and emphasised that in this system, the sensor and activator are the same thing: the cytoskeleton.

 

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Plane trees in the Parc de la Devesa

 

The room then discussed the future of physical approaches in biology. Would forces come to be as important to developmental and cell biologists as genetics and biochemistry had been in the last hundred years, for instance? If the answer to this question is yes (or even, as some biophysics nuts might have it, ‘much more important!’), a member of the audience raised a problem: from school onwards, scientists are trained to be biologists or physicists, without much overlap between the two. While some wanted the two disciplines to be much more integrated, others in the audience proposed that for some problems, the more important thing is to integrate the power of specialists. The ‘superdry’ mathematician who didn’t know cells were grown in liquid media until two years into a collaboration could nevertheless help wet biologists to better understand their cells with a model. The centenary of D’Arcy Thomson’s On Growth and Form next year will undoubtedly provoke further discussion as to the future of physics and biology.

 

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The Palau de Congressos de Girona. Source: www.gironacongressos.org

 

The meeting proper then began, in the chamber hall of the Palau de Congressos, a modern and well-designed conference centre near the chalky green river Ter. The place had real coffee. Having been to two meetings in the States this year2, it was like manna from heaven.

 

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Over the meeting’s three days, the three keynote lectures tackled different aspects of how brains are built and work. Claude Desplan (who it turned out was born nearby, on the French side of the Pyrenees) described his lab’s efforts in recent years to understand how the fly makes its medulla. Recent advances in single-cell sequencing – particularly drop-seq – were helping with the effort to categorise the identity and developmental pathways of the constituent neurons. The emerging picture was of an integration of spatial and temporal patterning systems in a rather rigid and determined manner. Magdalena Götz described her recent collaboration with Mark Hübener demonstrating that embryonic neurons can integrate amazingly well into injured adult brains, anatomically and functionally. She also described her collaboration with Victor Borrell, who in his own talk in the Neural Development session described a brief window in development that generates a massive number of radial glia cells, which then form a self-sustaining lineage to drive cortical expansion. Rainer Friedrich wanted to know how the architecture of neural circuits defined how the brain worked, how form provides function. He argued that uncovering a connectome was worthwhile for this aim and not just stamp collecting, and showed some stunning reconstructions of the zebrafish olfactory bulb derived from serial block face EM. This work required outsourced ‘tracers’ to manually track axons and synapses from EM slices; it seems AI is not near the task, yet.

 

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Some chimeric street art in Girona

 

There was a fascinating session on oscillations across life’s kingdoms. Paloma Mas talked about how different organs in the plant maintained their own circadian rhythms and how each clock influenced the others, while Jordi Garcia-Ojalvo gave a bacteriologists view of self organisation and oscillating patterns. He wanted to convince us that bacteria are a good model for developmental questions, and described how oscillations of growth in bacterial biofilms are driven by nutrient restriction and electrical communication. I was brought back to more familiar ground with Alexander Aulehla, and live imaging of the somitogenesis clock as it ticks in mouse embryos and cultured cells. “Information,” he said, “might be encoded not just in the presence or absence of a signal, but its phase and frequency.” His was one of many talks that used mathematical descriptions to try and understand patterning – another being Luis Escudero, who described how his lab was using Voronoi diagrams (yep, had to Google this!) to explain the distribution of cell shapes within a packed epithelium, and how pathological examples provided useful deviations from the normal distributions.

 

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Saint Narcís. By Desconegut – devocioteca.blogspot.com https://commons.wikimedia.org/w/index.php?curid=7916136

 

Since my PhD days studying wing development, I have always associated Spanish developmental biology with fly research. I was pleased to hear from Marco Milan about the legend of the flies of Saint Narcís, who in the 13th century protected Girona from the French troops that were besieging it. Judging by the drawings and the behaviour, maybe not Drosophila, but close enough!

700 hundred years later, flies were represented in the SEBD in plenty of posters and talks. Benjamin Prud’homme gave a neat story of how a species of Drosophila evolved male-specific spots on its wings, giving us an update on previous work. The message I took home from the talk was that a seemingly simple morphological change could have quite complex genetic underpinnings: it wasn’t as simple as just recruiting a pigment-promoting gene by evolving a new enhancer. Sofia Araujo described how a mutant found in a screen for defective tracheal development led to the discovery of a role for centrosomes in the branching of single cells, independent of any affect on mitosis. The idea is that the centrosomes act as microtubule organising centres to dictate cytoskeletal organisation and membrane behaviour. Isabel Guerrero also looked at cell membranes, and the thin extensions called cytonemes that promote cell signalling. She proposed that cell-cell contacts along the length of cytonemes promoted signalling in a synapse-like manner.

 

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Isabel Guerrero discussing cytonemes

 

I was delighted to hear the latest from Juan-Pablo Couso, whose lab was next door during my PhD and is soon to be moving from the UK to the CABD in Seville, a dedicated centre for developmental biology (something I don’t think we have here in the UK?). When I started my PhD, the Couso lab had just published their characterisation of tarsal-less, a Drosophila gene involved patterning and morphogenesis, the function of which is provided by a small open reading frame encoding a peptide only 11 amino acids long. Over the years, the lab have chased other smORFs, characterising specific functions in phagocytosis and calcium uptake, as well as taking genome wide surveys of their potential numbers. It’s a nice example of how a chance finding can radically alter the direction of a lab (the original tarsal-less allele was a spontaneous mutation). His talk ended by trying to situate smORFs into a cycle of gene birth and death over evolutionary time in the genome, which will be the subject of an upcoming review from the lab.

And these were some of my scientific highlights among a lot of fascinating work. I can only wish Spanish researchers a more stable financial future to continue it.

 

~

Girona itself turned out to be beautiful: old buildings, winding lanes, church bells. I ate well (not always a given at conferences), particularly in the final night at the conference meal in this place, got to watch Lionel Messi humiliate Pep Guardiola in a bar full of Catalans, and even take in some nightlife (scientists, it seems, dance the same the world over).


 

1 – I once spent a few months mapping somatic clones in the adult Drosophila wing onto templates, before prepping the wings for EM. I needed to know where the clone was, and whether it covered both surfaces of the wing or not, before mounting on the sticky EM stub. The first opportunity for disaster was a misplaced breath, launching the wings into orbit. The second was to mount the wings on the wrong side, which I would only realise after an hour setting up the EM in the cold and the dark. In retrospect, this was a breeze compared to CLEM.

2 – If you’re interested, you can read my previous reports from Boston and SouthbridgeGirona was my third conference representing the Node, and I’ve become used to the strange feeling of being in a new place knowing perhaps a handful of people but being familiar with the rituals – talk followed by questions followed by talk followed by questions, the phrases that have become almost clichés (“In my lab we’re interested in…”, “A very talented postdoc in the lab…”, “I hope I can convince you that…”), the coffee and the posters and the pastries, the emptiness of hotel rooms, the excitement of a new town. It makes me think we lack a literature or culture of conferences (or at least that I haven’t found one yet – any suggestions?)

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Postdoctoral Scientist in Fish Heart Regeneration – University of Oxford

Posted by , on 28 November 2016

Closing Date: 15 March 2021

Postdoctoral Scientist in Fish Heart Regeneration
Department of Physiology, Anatomy and Genetics, Oxford
Grade 7: Salary in the range £31,076 – £32,004 p.a.
Applications are invited for a Postdoctoral Research Scientist to join Professor Mathilda Mommersteeg’s laboratory to work on a project focussed on identifying the mechanisms underlying fish heart regeneration using the Mexican cavefish, Astyanax mexicanus. The post would be ideally suited to a postdoctoral scientist with experience in working with fish models and background expertise in heart development or regeneration.

The successful applicant will be specifically charged with performing QTL analyses to link the ability for heart regeneration to the genome, followed by functional validation of the identified loci. The main techniques in this project will include fish cardiac injury surgery, the generation of constructs for injection to generate transgenic zebrafish and Astyanax mexicanus lines using CRISPR, oocyte injections, western blotting, qRT-PCR, immunohistochemistry and in situ hybridisation.

You must hold, or be near completion of a PhD (or equivalent) in molecular biology, biomedical sciences, genetics or a related science and have experience of working with in vivo models of development and/or cardiovascular disease.

You will be based in the Sherrington Building in the Department of Physiology, Anatomy and Genetics at the University of Oxford.

The position is funded by an ERC starting grant for up to 5 years. The post is due to start on 1 March 2017.

The closing date for applications is 12.00 noon on Monday 19 December 2016. Interviews are likely to be held early January 2017.

https://www.recruit.ox.ac.uk/pls/hrisliverecruit/erq_jobspec_version_4.jobspec?p_id=126188 

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The 3D atlas of human development

Posted by , on 28 November 2016

“It’s fair to say that we currently know more about the moon than about our own embryonic development. The current textbooks all show the same kind of images based on a few embryonic specimens from the 1930s. Some of those are not even human embryos. New version of these books keep using those images, often without reference, only updating new molecular information”

This leads to the situation that the origin of the knowledge on human embryology became forgotten and that some of the knowledge was based on chicken, axolotl and mouse specimens. Moreover, the complex morphological changes during development cannot be well illustrated on the flat two-dimensional pages of text books.

To remedy this situation we proposed to use the sections of the embryos available in the Carnegie Collection to generate a comprehensive series of interactive 3D reconstructions of human embryonic development; a proposal that was based on the availability of 3D reconstruction and visualisation software.

 

 

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3D view of a reconstructed stage 20 human embryo, from Figure 2, de Bakker, et al. Science, 2016

 

This project, initiated by Professor Antoon Moorman, with dedicated financial support of the Academic Medical Center in Amsterdam, the Netherlands, was carried out by Bernadette de Bakker. The educational angle made that the project was ‘by students – for students’. De Bakker obtained a duplicate series of images of stages 7 to 23 (15 – 60 days of development) from the Carnegie Collection in Washington DC. After alignment in a 3D reconstruction program, a total of 75 medical students manually annotated every structure and organ in each of the about 15,000 images as part of their scientific internship; an effort that took more than 45,000 hours.

Another 15 students, this time from the game development faculty, then ‘modelled’ the resulting 3D reconstructions to reduce the complexity without losing biological detail. Their results, turned into 3D-PDF files, thus represent the actual morphology of the series of embryos in a format that can be easily interactively handled with the commonly used PDF reader. This was all supervised and supported by the expert embryologists of the department.

 

“The 3D Atlas and Database of Human Embryology is the first to present such a large amount of data based on such a large number of human embryos. With this atlas and database we are able to quantify very precisely embryonic growth and the growth and position of specific organs”

 

 

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Stage 17 embryo, scaled, from the interactive PDF available on the 3D atlas website.

 

The 3D atlas, that contains morphological reconstructions of 14 stages, is accompanied by a database with quantitative data based on 17 duplicate stages of reconstructed embryos. This database shows the total volume of the embryo grows exponentially with a constant volume increase of 25% per day. However, different organs grow with different growth rates, depending on their function during development. The project team established a tool to determine the position of organs relative to the developing vertebral column of the embryo. Application of this tool can help to solve ambiguities with respect to the relation between organs. The third series of data relates the chronology of human development to that of the mouse and the chicken. These data show that each species runs its own embryological script.

 

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Notochord development at Stage 9, from Figure 6, de Bakker, et al. Science, 2016.

 

Already during the construction of the atlas, discrepancies between the observed embryology and the embryology textbooks became apparent. The textbook descriptions of the development of the venous system and the notochord clearly show influence of knowledge dissipating from studies on lower vertebrates. Descriptions that could not be corroborated in the current reconstructions based on the real human substrate. The interactive 3D atlas, and the source images that are also available from the website, allow every user, be it student or biomedical specialist, to independently verify those discrepancies and form their own opinion.

 

“The atlas is useful because to study how congenital malformations appear it is important to know how normal human embryonic development occurs. Experimental embryologists will know how the changes in their experimental animals relate to the human situation. Scientists who study how toxic substances can affect embryonic development, are helped to refine the chick and mice models they work with. Moreover, also gynaecologists can use this atlas to show pregnant women how their child develops.”

 

Contributors: Bernadette de Bakker, Jan M Ruijter and Antoon Moorman


The 3D atlas of human embryology is available here: 

http://www.3dembryoatlas.com/

 

The Research Article in Science reporting the atlas is available here, Open Access:

http://science.sciencemag.org/content/354/6315/aag0053

 

 

 

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Sheffield STORM symposium – 11th Jan 2017

Posted by , on 25 November 2016

We are delighted to invite you to our one-day STORM symposium, which aims to bring together expertise from fields of biology and physics as well as microscope software engineers to discuss the challenge of Stochastic Optical Reconstruction Microscopy (STORM).

This symposium is aimed at those researchers who are currently using STORM. We aim to provide a platform for discussion and collaboration to highlight the problems researchers are facing with STORM; and together we can try to find solutions.

There will be talks from researchers, addressing issues such as sample preparation, labelling and image analysis. As well as talks from experts including Nikon, and those using the Thunderstorm imageJ plugin. We encourage you to bring along a A3/A2 poster of a current image. These images do not have to be perfect, please bring along images you are having problems with or have questions about. See website for details. The images will be displayed during the day to allow you to get feedback from other attendees and prizes will be awarded to the most interesting. Registration closes 8th January 2017 but places are limited.

 

Registration is now open – please check our website for details:

 

https://sheffieldstorm.wordpress.com

 

Attached is a flyer – please feel free to pass on to other interested parties at your Universities/Institutes:

 

storm-symposium-registration-flyer-oct2016

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A Fusion of Art and Science

Posted by , on 24 November 2016

Cytokinetic Abscission In the final step of cell division, the bridge connecting the cells is cut to give rise to two separate daughter cells – a fascinating process I have been working on since I started my PhD. This is a variation of my very first science-themed drawing, which I overlaid with an immunofluorescence staining labeling microtubules (green) and DNA (blue) – a combination of a hand-drawn illustration with real microscopy images that quite literally fuses science and art.

 

I have always loved science, and have always loved art – I combine these passions to illustrate scientific themes with an artistic twist. With my illustrations, I aim to highlight fundamental scientific aspects in an unconventional and refreshing way. I want to add some creativity to the conventional forms of scientific communication, with the aim to spark interest inside and outside the scientific community. I create my drawings for everyone to enjoy – for scientists to appreciate biological findings in a less serious way, and for non-scientists to grasp fundamental biological principles.

I used to draw a lot before studying Molecular Biology at the University of Vienna and the ETH Zürich in Switzerland. I recently completed my PhD in Daniel Gerlich’s group at the Institute of Molecular Biotechnology (IMBA), during which I made my very first science-themed drawing back in 2013. My PhD research focused on cytokinetic abscission, the final step of cell division (shown above, click on images for full size). When I showed that drawing as part of my scientific presentations, I realized that it sparked interest and tended to stay in people’s memories. This is when I discovered that adding an artistic twist to science creates a unique way to communicate science.

 

An Unconventional Take on Scientific Presentations.This picture was taken during my presentation for the Kirsten Peter Rabitsch Award, which I had the honor to receive for my PhD research earlier this year – in it you can see a new version of my very first science drawing.

 

Being part of an institute that encourages creativity has helped me immensely to develop my artistic approaches. I participated in yearly campus-wide ‘Art & Science’ contests, where I experimented with drawing portraits of my colleagues and making a dress to illustrate my research project.

 

When Devotion Begets Emotion. These portraits of my fellow PhD students illustrate the intense emotions researchers face in everyday life in the lab. These drawings were part of a contribution to the Art & Science contest at the Vienna Biocenter, for which my team received the first prize in 2013.

 

The ‘ESCRT’ Dress. Cytokinetic abscission is mediated by a machinery composed of the Endosomal Sorting Complex Required for Transport (ESCRT)-III, which forms polymers that constrict the intercellular bridge until the membranes split. I created this “ESCRT” dress to illustrate how ESCRT-III separates the emerging daughter cells during abscission.

 

I began pursuing scientific art after having my drawing selected for the cover and abstract book of the Cell Cycle Meeting in Cold Spring Harbor. The positive feedback I received there was an incredibly rewarding experience that encouraged me to start creating artwork for other people’s research as well as my own. Since then, I continue making scientific illustrations, one of which was recently featured on the EMBO Journal cover.

 

EMBO Journal Cover. This EMBO Journal cover accompanies a paper on mammalian brain development I was involved in during my Master’s Thesis. The compass represents how the angle of the mitotic spindle in dividing cells affects their ultimate position within the brain – similar to a compass guiding the way to a location on a map.

 

I also began making artistic interpretations of recent scientific discoveries. Below is a small gallery of my illustrations for press releases that highlight recent publications.

 

 

Aside from highlighting research findings, I also began making illustrations for other purposes. For a popular science magazine, I created a less serious drawing illustrating the myth of the “five-second rule”, which suggests that bacteria will wait patiently before contaminating food that has been dropped on the ground.

 

Five-Second Rule.  Illustration for an article in the German version of Scientific American ‘Spektrum der Wissenschaft’.

 

I also had the wonderful opportunity to design the poster for the PhD symposium at the Vienna Biocenter titled ‘Mind the App’, as part of the organizing committee. For this illustration, as well as many of my others, I started by making a hand-drawn black and white sketch using pencils, and overlaid the colors digitally afterwards. I then added the apps on the phone to highlight the diverse applications of basic research that were covered at the conference.

 

Mind the App. Basic research gives rise to many ‘applications’. Poster of the ‘Mind the App’ VBC PhD Symposium at the Vienna Biocenter.

 

When I first started drawing, I mainly focused on creating portraits – in this illustration I got back to my roots to make a short animation about everyday life in the lab.

 

Failed Experiment. An unsuccessful experiment can bring up very intense emotions, which every scientist is certainly familiar with. I created these drawings for an animation to be used in a video for the PhD Program at the Vienna Biocenter

 

I love the challenge of capturing the essence of scientific discoveries in an aesthetic and abstract way, and I am very excited for many more artistic adventures to come. Every drawing is an experiment!

 

Check out my website (www.beatascienceart.com) for recent updates and a complete gallery.
 
All images © 2016 Beata Edyta Mierzwa

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New meeting: Programming and Reprogramming the Brain

Posted by , on 24 November 2016

On April 3-4, 2017 scientists from around munich-neuro-banner-300x250Europe will be converging on Munich, Germany for the next meeting in the Abcam Brain meeting series – Programming and Reprogramming the Brain. Organizers, Benedikt Berninger (Johannes Gutenberg University Mainz) and Paola Arlotta (Harvard University) have put together a fantastic line up of speakers (see preliminary program).

 

This two-day meeting will provide a forum for presentations and discussions on the emerging field of brain development, reprogramming and modeling with a focus on new genome wide tools to understand biological processes with single-cell resolution.

 

Call for abstracts

Talk and poster places are available, so don’t wait, submit your abstract today!

  • Talk deadline: December 15, 2016
  • Poster deadline: February 6, 2017

We hope to see you in beautiful Munich next year!


Meeting topics

  • Modeling human brain development from pluripotent stem cells
  • Programming and maintenance of cell identity in the CNS
  • Development-inspired reprogramming of the brain
  • Decoding CNS complexity with single-cell resolution
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eLearning at eMouseAtlas

Posted by , on 24 November 2016

A new eLearning resource that provides short and interactive vignettes in embryo (primarily vertebrate) development, from gametogenesis through to organogenesis, is available from the eMouseAtlas1,2 website (www.emouseatlas.org).

The current eLearning content are the tutorials produced by Professor José García Monterde of the University of Córdoba, and the presentation from collaboration between Professor Monterde and the eMouseAtlas project.

The resource describes the development of various anatomical systems including the cardiovascular system, nervous system, and musculo-skeletal system, and additionally introduces core developmental biology concepts such as gastrulation, placentation, and the formation of the germ layers.

 

eLearning combines animations that enable conceptual understanding of key principles of embryonic development with 3D visualisations of embryo anatomy.

 

eLearning Topics

 

The resource combines illustrative animations of embryonic development with interactive 3D visualisations of mouse developmental anatomy. The newly developed 3D viewer enables arbitrary sections to be sliced through embryo models.

 

The eLearning tutorials additionally link to gene expression patterns associated with developing organ systems, the cellular-resolution eHistology atlas and the DMDD (DMDD.org.uk) database of embryonic lethal phenotypes.

 

eLearning is freely available for both teaching and research purposes. eMouseAtlas continues to develop tools and resources that enable students and researchers to understand the concepts underpinning embryonic development. In this context we are willing to host learning materials on behalf of the community.

 

References

  1. Armit C, Richardson L, Hill B, Yang Y, Baldock RA (2015) eMouseAtlas Informatics: Embryo Atlas and Gene Expression Database. Mamm Genome. 26:431-40. doi: 10.1007/s00335-015-9596-5
  2. Richardson L, Venkataraman S, Stevenson P, Yang Y, Moss J, Graham L, Burton N, Hill B, Rao J, Baldock RA, Armit C (2014). EMAGE mouse embryo spatial gene expression database: (2014 update) Nucleic Acids Res. 42(1):D835-44. doi: 10.1093/nar/gkt1155
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Technical Research Assistant II. Pourquie lab. Harvard Medical School/Brigham and Women’s Hospital

Posted by , on 23 November 2016

Closing Date: 15 March 2021

Job Location: Brigham and Women’s Hospital, Development of Musculo-Skeletal Axis/Pourquié Lab, Boston MA

JOB SUMMARY:

Working under the general supervision of the Principal Investigator and on a day-to-day basis instructed by the Lab manager and Project supervisor(s) to contribute to research activities and lab operations to reach scientific goals. In accordance with established hospital policies and procedures, executes experiments involving in vitro protocols and cellular models for research studies targeting skeletal muscle, spine, dermis (paraxial mesoderm) development. Work additionally with in vivo embryo experimental systems (mouse, chicken). In addition, responsible for maintaining a moderately complex murine colony, laboratory supply inventory, cell culture room operation, and supporting lab safety compliance.

Principal duties and responsibilities will be:

  1. Conducts research protocols autonomously and/or in team involving in vitro protocols and cellular models for research studies targeting skeletal muscles, spine and dermis (paraxial mesoderm) development.
  2. Using aseptic technique, maintains tissue cultures and manipulates cell lines in a variety of complex experimental conditions including live-cell microscopy/imaging, library screens, and flow cytometry.
  3. Tasks include processing cell culture, embryonic tissue for live-cell or histologic examination and conducting subsequent immunohistochemical and molecular analyses. Perform procedures such as DNA extraction, conventional PCR and real time PCR, western blotting, and time-lapse imaging.
  4. Establishes and maintains a moderately complex mouse colony for the laboratory with responsibility for proper care, counts, inventory. May performs injections, some surgical procedures, microdissection and necropsy, following established and approved protocols. In collaboration with Project supervisor(s) , establishes new and modifies existing research methodologies and protocols.
  5. Collect and Analyzes data , assists with data preparation toward manuscript publication and grant applications.
  6. Documents accurately experimental work and research output
  7. Reports and discusses progress of work regularly with Project supervisor and Principal Investigator.
  8. Maintains lab supplies and reagent inventories
  9. Coordinates lab compliance with institutional policies and procedures in the areas of safety, environmental and infection control, under Lab manager supervision
  10. Assist in orientating and training new lab members, rotation students in area of expertise when required.
  11. Perform all other duties and responsibilities as directed, including both research and administrative duties.

Qualifications:

  • Master of Science in a biological science required.
  • Minimum 3 year hands-on experience with cell culture assays, preferably pluripotent stem cells.
  • Experience with laboratory mouse colony maintenance helpful, but not required.

Skills/Abilities/Competencies Required:

  • Sound analytical and organizational skills.
  • High degree of computer literacy.
  • Careful attention to detail with good, detail-oriented observational skills.
  • Willingness and ability to conduct in vivo (mouse) experiments.
  • Excellent oral and written communication skills.
  • Must have sound interpersonal skills. Ability to constructively interact with members of a research team to pursue scientific goals is a necessity.
  • Ability to work closely with Project supervisor (s)

Working Conditions:

  • Normal research laboratory environment.
  • Exposure to laboratory reagents, chemicals, and animal and human tissues under controlled conditions. Minimal risk when following established protocols and federal, state, and hospital guidelines.

 

To apply to this position please send your resume and cover letter to jchal@partners.org

 

 

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Two opportunities at The Company of Biologists

Posted by , on 23 November 2016

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The Company of Biologists is a not-for-profit publishing organisation dedicated to supporting and inspiring the biological community. We currently have two opportunities available in our Cambridge office.

 

Journal Website Content Manager

We are creating an exciting new role to enhance the community content on our journal websites.

We publish five important journals that serve the biological research community. All have effective publishing platforms and a good social media presence. We now seek to extend our community engagement, raise awareness of our charitable activities and build connections with early career scientists.

Read more here

 

Intern for Disease Models & Mechanisms

DMM is looking for an enthusiastic intern who wishes to gain experience in science publishing, including writing press releases, contributing to our social media activities, and supporting our Reviews Editor with commissioned articles. The internship is envisaged to last for 9 months at a salary of £20,000 per annum pro rata.

Our interns have a great track record of continuing on into important publishing roles.

Read more here

 

You can learn more about what The Company of Biologists does here:

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The elusive hematopoietic stem cells of Drosophila.

Posted by , on 22 November 2016

Drosophila hematopoiesis shows striking resemblance with that of vertebrates, both at the level of signalling molecules and the phase of development. Even though there has been no report of Hematopoietic stem cells (HSCs) in Drosophila, this model has been employed extensively to understand progenitor biology and niche interactions. The Drosophila blood cells are specialised precursor cells (present within the hematopoietic organ: the lymph gland), that show several similarities with stem cells. They are known to differentiate into mature blood cells of the fruit fly. Our new study identifies the “founder cells” or the “stem cells” that give rise to these specialised blood-progenitors.

 

How it started off:

Our team was involved in detailed characterisation of signals which are required for the maintenance of the larval hematopoietic niche. To understand the dynamicity of the expression pattern of a battery of niche markers, we ventured into dissecting the larval lymph gland of the early first instar. Analysing a newly emerged larvae, about 8 hrs old, we encountered a group of large cells that always aligned themselves near the dorsal vessel or larval heart. We started calling them “Big Cells”. It turned out that these cells expressed several markers seen in other described stem cells.

 

Founder Cells or HSCs:

The very fact that they stood out almost every time in a early instar lymph gland caught our attention, and we felt tempted to characterise them. Our attempt to trace them throughout development revealed that although the “Big Cells” do not die, they could not be tracked beyond 22 hours post hatching. We argued that maybe they were changing their fate. Indeed, on lineage tracing of these cells and analysing them at various time point of development, we could see that they are actually converted to blood progenitor cells. Analysing the same genotype at mature third instar larval stages indicated that not only progenitors but also differentiated cells are lineage traced. This clearly indicates that the “Big Cells” are multi-potent in their nature. As a functional correlate, we genetically ablated the “Big Cells” and analysed the consequence on the mature lymph gland. Remarkably, the elimination of these 4-5 “Big Cells” drastically reduced the size of the gland.

 

dotnode
The first instar larval lymph gland with the HSCs and its Niche marked by Dorothy-GFP expression

 

The final climax:

At this point we were thrilled that we had a fine story to tell about the elusive founder cells of Drosophila lymph gland. But a stem cell story without niche is not complete! We therefore entered into a spree to nail down the niche and the signal. Our suspicion was on the already described progenitor niche known to maintain the precursor cells. Since this niche is specified in embryo and is the most differentiated cell type in the first instar lymph gland, we speculated that it might also be serving as the niche for the HSCs. Our expression studies demonstrated that HSCs are enriched in phosphorylated Mad (pMAD), a pathway effector of Dpp signalling. To start with, therefore, we down regulated pMad from the HSCs. This resulted in their disappearance and a concomitant reduction in lymph gland size. Strikingly, on knock down of Dpp signalling from the progenitor niche, the HSCs failed to self-renew, clearly validating that Dpp signalling from the progenitor niche is its source of sustenance. It is to be noted that vertebrate early HSCs are also maintained by BMP (vertebrate counterpart of Dpp) signalling.

 

What are the implications:

With the identification of the early HSCs and the signal that maintains in Drosophila larvae, we have not only demonstrated the conservation with vertebrates, but put forward a model that can be used for answering several questions pertinent to vertebrate early blood development, both in normal as well as aberrant conditions.

 

MAIN PAPER:
Dpp dependent Hematopoietic stem cells give rise to Hh dependent blood progenitors in larval lymph gland of Drosophila. 10.7554/eLife.18295

 

References:

Drevon, C., and T. Jaffredo. 2014. “Cell interactions and cell signaling during hematopoietic development.” Exp Cell Res 329 (2):200-6. doi: 10.1016/j.yexcr.2014.10.009.

Durand, C., C. Robin, K. Bollerot, M. H. Baron, K. Ottersbach, and E. Dzierzak. 2007. “Embryonic stromal clones reveal developmental regulators of definitive hematopoietic stem cells.” Proc Natl Acad Sci U S A 104 (52):20838-43. doi: 10.1073/pnas.0706923105.

Evans, C., Olson, J., Ngo, K., Kim, E., Lee, N., Kuoy, E., Patananan, A., Sitz, D., Tran, P., Do, M., Yackle, K., Cespedes, A., Hartenstein, V., Call, G., & Banerjee, U. (2009). G-TRACE: rapid Gal4-based cell lineage analysis in Drosophila Nature Methods, 6 (8), 603-605 DOI:10.1038/nmeth.1356

Evans, C.J., Sinenko, S.A., Mandal, L., Martinez-Agosto, J.A., Hartenstein, V., & Banerjee, U. (2007). Genetic Dissection of Hematopoiesis Using Drosophila as a Model SystemAdvances in Developmental Biology, 18, 259-299 DOI: 10.1016/S1574-3349(07)18011-X

Jung, S. H., C. J. Evans, C. Uemura, and U. Banerjee. 2005. “The Drosophila lymph gland as a developmental model of hematopoiesis.” Development 132 (11):2521-33. doi: 10.1242/dev.01837.

Mandal, L., Banerjee, U., & Hartenstein, V. (2004). Evidence for a fruit fly hemangioblast and similarities between lymph-gland hematopoiesis in fruit fly and mammal aorta-gonadal-mesonephros mesoderm Nature Genetics, 36 (9), 1019-1023 DOI: 10.1038/ng1404

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