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Book review: Life and the matrix

Posted by , on 13 December 2012

This book review originally appeared in Development. Charles Streuli reviews “Extracellular Matrix Biology ” (Edited by Richard O. Hynes and Kenneth M. Yamada).

Book info:
Extracellular Matrix Biology. Edited by Richard O. Hynes, Kenneth M. Yamada Cold Spring Harbor Laboratory Press (2012) 387 pages ISBN 978-1-936113-38-5 $67.50 (hardcover)

To be metazoan is to have an extracellular matrix (ECM). ECM components evolved simultaneously with animals and provided the architectural scaffold onto which multicellularity could emerge several hundred million years ago. From a primitive basement membrane toolkit and the primordial fibrillin and thrombospondin genes that allowed the evolution of multilayered animals, successive gene duplications and crises permitted the appearance of protostomes and deuterostomes, leading to vertebrates and eventually to us. Along the way, the evolutionary shuffling of pre-existing and novel protein domains to form tenascins, fibronectin and other matrix proteins coincided with the emergence of neural crest, vasculature and the nervous systems that characterise chordates and advanced vertebrates. Coinciding with this, metazoans evolved complex plasma membrane machines containing adhesome proteins that link the ECM to the cytoskeleton and intracellular signalling pathways.

Core ECM proteins make up ∼1.5% of the mammalian proteome. This enormous parts-list of around 300 matrix proteins, newly christened the ‘matrisome’, highlights the diverse and extraordinary roles of the matrix in metazoan biology. ECMs range from pericellular matrices, such as basement membranes, to the grander structures of connective tissue that give organs their shape, and the tendons, cartilage and bones that bestow humans and animals with their form. It is therefore not surprising that the ECM pervades every aspect of metazoan life. The matrix is essential for early embryonic development and it regulates nearly every facet of cell behaviour. Moreover, altered ECM and ECM-cell interactions lie at the root of many diseases, including cancer, diabetes, inflammatory disorders and osteoarthritis.

The ancient history of the association between the ECM and cells effectively means that the two are inseparable. Although the prosaic view of cells is that they end at the plasma membrane, the cell and its pericellular matrix are actually a continuum in all complex animals. A cell’s ECM coat provides the architectural hardware for cell positioning and migration, which is meshed together with intracellular cytoskeletal networks by myriad components of the adhesome. The matrix enables a first-pass checkpoint for growth and developmental signals, it is the vehicle for morphogenetic gradients in development, and it is the spatial rheostat for intracellular signalling pathways. ECM receptors thus convert both chemical and physical extracellular inputs to determine cell survival, proliferation, migration and tissue-specific gene expression.

A book on such a profoundly important topic requires a clear vision of the breadth of the ECM and its roles in development, cell and tissue function and disease. Extracellular Matrix Biology has been organised by two of the most eminent scientists in the ECM research field, Richard Hynes and Kenneth Yamada, and, predictably, the book hits the mark. This volume, one in a series from Cold Spring Harbor Laboratory Press, contains a superb collection of review articles. Well-known opinion-makers in the field have written the chapters, which are detailed, authoritative and up to date. The organisation of the book is sensible, beginning with an overview of the matrisome and its evolution, and then working through the key ECM components, basement membranes, collagens, proteoglycans, tenascins, thrombospondins and fibronectin. This is followed by chapters on integrin activation, genetics, and links with TGFβ, as well as adhesion complexes, mechanotransduction, and matrix remodelling. Towards the end, links between ECM and tissues are considered, with chapters on cell migration, embryonic development, angiogenesis, skin, and the nervous and haemostatic systems. I am slightly disappointed that mucins have been omitted, as they are crucial components of the pericellular matrix, but nevertheless the coverage in the book is excellent overall.

Looking through my (rather dusty) volume of Betty Hay’s Cell Biology of Extracellular Matrix (2nd edition, 1991), which was one of the last comprehensive books on ECM, it is startling to see how many advances have been made since then. Prior to our era of genomics, knockouts and dynamic imaging, much of the knowledge about ECM was based on biochemistry and cytology. Disease associations with altered ECM were known, but many of the molecules involved had not been identified and mechanisms were largely unexplored. Little was understood about the structures of matrix molecules or their receptors, and there was only an indication that integrins could transmit signals from the ECM to the cell interior. It is also interesting that the focus of illustrations has largely switched from electron microscopy images and some relatively sketchy diagrams to detailed lists of ECM components, domain organisations, interaction networks, disease associations, and mouse and human mutations. This new book is therefore a timely addition, and many of the chapters also consider where the field is going now and what unknowns might be unravelled in the cell-matrix field over the next 20 years. Overwhelmingly, the shift in focus from the organisation of the ECM in tissues, to cataloguing its vast array of constituents and interactions with cells, indicates that a central challenge is to understand how all the matrix and adhesion components fit together and how they control cell fate and function.

Although crystal ball gazing is inevitably difficult, there are certainly some exciting opportunities that are alluded to in the book. The emerging awareness that biology occurs in four dimensions and is completely dependent on the ECM (incidentally, this was well understood by Hay) will undoubtedly be a major focus for cell-matrix research at least for the next few years. For example, knowledge of how matrices are assembled in 3D and remodelled in 4D is beginning to appear. Most cells function within communities, often of different cell types, and we are just beginning to understand how the matrix influences cell function and dynamics in 4D and how different cell types use the ECM to communicate, e.g. via stromal-epithelial interactions. The notion that the physics of the ECM profoundly influences cell and tissue function is fuelling new research on how forces are built into ECMs, how they are sensed by cells, and how they are converted to chemical signals that control transcription and cell fate. The structures of ECM proteins and some adhesion signalling proteins have been solved (some only at low resolution), leading to a new focus on atomic interactions at the protein-protein interface. ECM and adhesion receptors are crucial regulators of the immune system, and the dawn of immunomatrix biology is changing the thinking about immunological control. And, most profoundly, the basic discoveries of cell-matrix research are yielding novel small-molecule, bioengineered and genetic therapies for the vast array of diseases caused by altered ECM and interactions between the cell and the matrix. For example, there are no effective cures for osteoarthritis beyond surgery; advances in this (and other) areas using genetic analysis based on genome-wide association studies and systems biology are needed to dissect all of the component parts that cause debilitating diseases of injury and old age, and thereby to develop new treatments.

One of the challenges posed by reviewing this book was to ask who it is for. The original chapters appeared over several months in the online publication Cold Spring Harbor Perspectives in Biology, and they have now been collated for the book. Although some of the articles are available online (depending on your library’s subscription), by combining them in a single volume the editors have created a very nice resource that will provide a valuable reference work for several years to come. I would recommend those entering the field of cell-matrix biology, as well as those already in it, to read the book from cover to cover. The ECM is now understood as being so much more than a tissue scaffold and a precursor for building bones, and this new book definitively indicates where the field is now and where it is going. The intimate connections between the ECM and most cellular processes in animal development are gradually being recognised by mainstream biologists, and this could be accelerated when the key advances in this book are used to update current undergraduate texts on cell biology. At a broader level, once some of these concepts are incorporated within school biology education, then we’ll know that ECM biology has truly come of age.

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Would you like to work for the Node?

Posted by , on 13 December 2012

As you may have spotted, we’ve just posted a job ad for community manager for the Node. That is currently my job, but I will be leaving at the end of February, so there will be a vacancy.

I’ve had this job since the Node launched, and even before then! I’ve had a great time setting up the site, meeting so many scientists around the world, and seeing the Node grow from nothing to a well-visited resource for the developmental biology community. You’ve all been great to work with, but now it’s time for me to move on, and for someone else to take over. Have a look at the job ad and apply if you’re interested. The office is based in Cambridge, UK. We… erm, I mean THEY are actually moving to a nice new office in a few months, too. The company publishes five journals, so you’ll learn a lot about publishing while you’re here as well.

For everyone else, to make it easier on the next community manager and in the transition phase, please remember that you do not need to ask for permission to post on the Node. If your account is approved, you can post. I’ve personally been okay with reading over some posts for grammar and spelling if you’ve asked me to, but this is really not necessary. The concept of the Node is such that you can share news without editorial input. Take advantage of your freedom to post!

My new job will be in London, and still in the scientific publishing-adjacent field, so I’m not going far, but I won’t be involved with the Node anymore. If you’d like to stay in touch with me, and find out what I’m doing next, your best bet is to find me on Twitter as @easternblot.


(Image: Wordle cloud created from the archive of monthly highlight posts)

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Categories: Careers, News

Community Manager for the Node

Posted by , on 13 December 2012

Closing Date: 15 March 2021

The Company of Biologists and its journal Development are seeking to appoint a new Community Manager to run its successful community website the Node and the journal’s social media activities.

Launched in 2010, the Node is the place for the developmental biology community to share news, discuss issues relevant to the field and read about the latest research and events. We are now looking for an enthusiastic and motivated person to develop and maintain the site.

Core responsibilities of the position include:

–       Creating and commissioning content for the Node, including writing posts and soliciting content from the academic community, societies and other organisations
–       Providing creative and practical input into the development of the site
–       Maintaining and developing Development’s and the Node’s presence on social networking sites such as Facebook and Twitter
–       Contributing non peer-reviewed content to the journal
–       Representing Development and the Node at international conferences
–       Contributing to the Company of Biologists’ outreach activities

The successful applicant will have:
–       Research experience in the biological sciences, ideally a PhD in developmental or stem cell biology
–       Proven blogging and social media skills, ideally including experience with WordPress
–       A clear understanding of the online environment as it applies to scientists
–       Excellent writing and communication skills
–       Excellent interpersonal and networking abilities – both online and in person

This is an exciting opportunity to develop an already successful and well-known site, engaging with the academic, publishing and online communities. The Community Manager will work alongside an experienced and growing team, including Development’s Executive Editor, as well as with the journal’s international team of academic editors. Additional responsibilities may be provided for the right candidate. The position will be based in our office in Cambridge, UK.

The Company of Biologists (www.biologists.com) is a not-for-profit organisation, publishing five journals in the biological sciences: the three established journals Development, Journal of Cell Science and The Journal of Experimental Biology, as well as two newer Open Access journals, Disease Models & Mechanisms and Biology Open. The organisation has an active programme of charitable giving for the further advancement of biological research, including travelling fellowships for junior scientists and contributions to academic societies and conferences.

Applicants should send a CV along with a covering letter that summarises their relevant experience (including, if possible, links to online activities), salary expectations, and why they are enthusiastic about this opportunity.

Applications should be sent by email no later than January 20th 2013 to miriam@thecob.co.uk
Informal queries to Miriam Ganczkowski on +44 (0)1223 426 164
Applicants should be eligible to work in the UK.

 

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December 13

Posted by , on 13 December 2012

Today’s recommended paper is:

Offspring from Oocytes Derived from in Vitro Primordial Germ Cell-like Cells in Mice
Katsuhiko Hayashi et al. (2012)
Science 338 (6109), 971-975

Submitted by Eva Amsen:
“I saw Mitinori Saitou present this work at the EMBO meeting and it made me realize how far this fast-moving field has already come.”

From December 1 to 24 we are featuring Node readers’ favourite papers of the past year. Click the calendar in the side bar each day to see a new paper. To see all papers submitted so far, see the calendar archive.

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Don’t get rid of the middleman

Posted by , on 12 December 2012

There are a lot of situations in life where the “middleman” is unnecessary and costly.  In cells, that middleman is necessary and fascinating at the same time.  The sequence of DNA to middleman mRNA to protein provides our cells with countless ways to regulate complex events, including those surrounding stem cell divisions.

When stem cells divide, one daughter cell maintains stem cell characteristics while the other daughter cell follows a path towards differentiation.  Before differentiation, this cell can divide several times during a stage called transit-amplification.   In the fruit fly testes, the division of the germline stem cell (GSC) produces another GSC and transit-amplifying cells called spermatogonial cells.  Spermatogonial cells begin differentiating as they pass through the spermatocyte stage on their way to becoming sperm.  A recent paper in the journal Development investigates the regulation of a key differentiation factor, Bam (Bag of marbles), during this transition.  Bam protein is found in spermatogonial cells, but is not found in the later spermatocyte stage (yet bam mRNA is present).  According to Eun and colleagues, post-transcriptional regulation of Bam levels occurs through microRNA binding at the bam 3’UTR.  Overexpression of the two microRNAs involved delayed the proliferation-to-differentiation transition, while failure of Bam down-regulation caused differentiation problems leading to male sterility.  The images above show fruit fly testes stained to show the GSC hub (small red hub), spermatocytes (green) and Bam protein (red, white in inset images).  In a control testis (left), Bam protein is found in spermatogonial cells near the GSCs.  When the bam 3’UTR sequence was replaced with the 3’UTR of a constitutively expressed tubulin gene, Bam protein is found throughout spermatocytes as well.

For a more general description of this image, see my imaging blog within EuroStemCell, the European stem cell portal.

EResearchBlogging.orgun, S., Stoiber, P., Wright, H., McMurdie, K., Choi, C., Gan, Q., Lim, C., & Chen, X. (2012). MicroRNAs downregulate Bag of marbles to ensure proper terminal differentiation in the Drosophila male germline Development, 140 (1), 23-30 DOI: 10.1242/dev.086397

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December 12

Posted by , on 12 December 2012

Today’s recommended paper is:

A Mechanoresponsive Cadherin-Keratin Complex Directs Polarized Protrusive Behavior and Collective Cell Migration
Gregory F. Weber, Maureen A. Bjerke and Douglas W. DeSimone (December 2011)
Developmental Cell 22 (1), 104-115

Submitted by Katherine Brown

“This beautiful paper uses cadherin-coated magnetic beads applied to single Xenopus gastrula cells in culture to demonstrate that tension polarises the cell and determines the direction of migration, and to investigate the mechanosensory pathway involved. The work exemplifies our increasing appreciation of the role that physical forces have in determining cell and tissue behaviour during development.”

From December 1 to 24 we are featuring Node readers’ favourite papers of the past year. Click the calendar in the side bar each day to see a new paper. To see all papers submitted so far, see the calendar archive.

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Skate wins again

Posted by , on 11 December 2012

Remember the skate image by David Gold, Lynn Kee, and Meghan Morrissey of the 2011 Woods Hole embryology course? It won the cover competition in April, and appeared on the cover of Development issue 139(12).

Today, at the Company of Biologists Christmas lunch, we held a small inter-journal cover competition. Over the past few weeks, all our colleagues from Development, Journal of Cell Science, Biology Open, Disease Models and Mechanisms and the Journal of Experimental Biology voted for their favourite (and least favourite) covers submitted by editors of each journal. Development had submitted the skate cover – and won! It was a close race with JEB’s chameleon cover.

Of course this was all YOUR doing. Thanks David, Lynn, and Meghan for taking the image, and thanks to everyone else for voting it onto the cover. You helped us win chocolate for the office!

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Nobel Laureates Warn Against Going over the Fiscal Cliff

Posted by , on 11 December 2012

Although I’m not a fan of simply reposting press releases, this press release from The Coalition for the Life Sciences, about a letter-campaign by Nobel Laureates to emphasize the importance of research funding, is worthy of a read. The coalition is made up of several scientific organisations that overlap with the Node’s readership (ASBMB, ASCB, GSA, HHMI, SfN, and ASCI). While the press release is focused on the US, cuts in research funding in the US will indirectly affect us all.


FOR IMMEDIATE RELEASE December 10, 2012
Nobel Laureates Warn Against Going over the Fiscal Cliff

Bethesda, Maryland – Nobel Laureates from across the country are warning Congressional leaders and President Obama about the danger the fiscal cliff poses to research and innovation.
Starting December 3, the Coalition for the Life Sciences has sent a letter a day from a Nobel Laureate in either Chemistry or Physiology and Medicine. Twenty Nobel Laureates are engaged in this campaign. In these letters, each Laureate emphasizes the importance of federally funded research and the dire consequences of funding cuts. Of particular concern, the National Institutes of Health (NIH) will face an 8.2% across-the-board cut starting January 1, 2013, if Congress and the Administration refuse to agree on solutions to the fiscal cliff.
Coalition Board member H. Robert Horvitz, from the Massachusetts Institute of Technology, shared the 2002 Nobel Prize in Physiology or Medicine. He said, “This potentially very deep cut to the NIH as well as to all other federally-funded science would negatively impact job creation and seriously jeopardize the long-standing leadership position of the U.S. in research and innovation.”
Paul Berg, from Stanford University and the co-recipient of the 1980 Nobel Prize in Chemistry, agreed. “Past support of the NIH by the United States Congress has enabled the American scientific enterprise to rise to world leadership in the physical and life sciences. It is also why Americans have dominated as recipients of the Nobel and other illustrious Prizes.”
All the Nobel Laureates are concerned that cuts to the NIH will stifle discoveries that improve health, save lives, and drive our economy. NIH supports scientists and their critical work in every state across the nation, which means that every state would feel the negative effects of going over the fiscal cliff. Laboratories would shut down, scientists would be laid off, and local businesses that support research would close. Progress on developing promising new cures would slow, if not stop outright.
Coalition Director Lynn Marquis said the campaign arose from a shared anxiety among Coalition members about the future of the nation’s leadership in scientific output and innovation. “We felt strongly that voices from the scientific community needed to be heard and the Nation’s Laureates provide a unique voice that adds gravitas to the debate in Washington.”

 

The Coalition for the Life Sciences is an alliance of six non-profit professional organizations working together to foster public policies that advance basic biological research and its applications in medicine and other fields. For further information, please call Lynn Marquis, the Director of the CLS, at (301) 347-9309 or visit www.coalitionforlifesciences.org

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Categories: Funding, News

December 11

Posted by , on 11 December 2012

Today’s recommended paper is:

Free Extracellular Diffusion Creates the Dpp Morphogen Gradient of the Drosophila Wing Disc
Shaohua Zhou et al. (2012)
Current Biology 22 (8), 668-675

Submitted by Barry Thompson:
“This paper overturns the idea that the Dpp morphogen moves by transcytosis.”

From December 1 to 24 we are featuring Node readers’ favourite papers of the past year. Click the calendar in the side bar each day to see a new paper. To see all papers submitted so far, see the calendar archive.

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December 10

Posted by , on 10 December 2012

Today’s recommended paper is:

A Human Stem Cell Model of Early Alzheimer’s Disease Pathology in Down Syndrome
Yichen Shi et al. (2012)
Science Translational Medicine 4 (124), 124ra29

Submitted by Claire Cox:
“I found this paper fascinating as it demonstrates the potential of iPSC technology for studying disease pathology in culture. Generating cortical neurons from iPSCs and ES cells that have signs of Alzheimer’s Disease is remarkable and could pave the way for future studies such as drug screens.”

From December 1 to 24 we are featuring Node readers’ favourite papers of the past year. Click the calendar in the side bar each day to see a new paper. To see all papers submitted so far, see the calendar archive.

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