Recognizing scientific excellence in the biology of cell adhesion
© Wary; licensee BioMed Central Ltd. 2005
Received: 08 March 2005
Accepted: 18 April 2005
Published: 18 April 2005
The prestigious 2005 Japan Prize for Cell Biology has been awarded to Dr. Masatoshi Takeichi, Director of RIKEN Developmental Biology, Kobe, Japan, and Dr. Erkki Ruoslahti, Distinguished Professor, The Burnham Institute, La Jolla, USA for their "Fundamental contribution in elucidating the molecular mechanisms of cell adhesion". The award is scheduled to be presented to the scientists in ceremonies in Tokyo on April 20, 2005 as part of a week-long celebration of "Japan Prize Week".
What is cell adhesion?
Well, why does our skin look so smooth on the surface? How do skin cells adhere to each other and the underlying connective tissue to resist wound and bruise? How do two 'unlike' or 'like' cells live side-by-side? How are muscles and tendons glued to the bones? How do endothelial and epithelial cells are separated from each other? What mechanisms divide astrocytes, neurons, and the endothelial cells that make up the neurovascular unit? The answer is "cell adhesion", which is because of the characteristic properties of proteins and molecules that act like 'glue' or 'sticky molecules'. If cells or tissues do not hold each other, like in blistering skin in which something as gentle as a human touch can cause the skin to blister and peel away, inviting fatal infection and wound that may never heal. Suffice to say, the chances of survival will be somewhat diminished.
What are cell adhesion molecules?
In the late 1970's two ideas were put forward. First, the chemoaffinity hypothesis proposed that cell-cell contacts are mediated by unique set of cell adhesion molecules presented by adjacent cells. Second, adhesion molecules are limited, but their affinity could switch from low to high and vice versa. Soon afterwards, several important cell adhesion molecules were discovered and described including the cadherins, neuronal cell adhesion molecules (NCAM), extracellular matrix (ECM) molecules, proteoglycans, the immunoglobulin cell adhesion molecules, junctional adhesion molecules (JAMs), connexins, and selectins. Those ideas are very much alive and many cell adhesion molecules discovered recently are being tested with stringent criteria with better technologies today.
How do these molecules promote cell adhesion?
Cell-aggregation and cell adhesion assays
Cell biologists use proteolytic enzymes such trypsin and Ethylenediaminetetra-acetic acid (EDTA) to detach/disaggregate cells from the culture dishes and to prepare of primary cells from intact tissues. Trypsin is a proteolytic enzyme, while EDTA, a metal ion chelator. When used in right combination, they can disrupt both cell-cell and cell-matrix interactions, that is to say these two substances can disaggregate cells and tissues . Cell-cell and cell-matrix interactions appear to go hand-in-hand [Fig. 2]. Upon attachment adherent cells sense presence of Calcium in the environment, calcium is required for both cell-cell and cell-matrix interactions. Dr. Takeichi described as to how cell-cell interactions between "like" cells and "unlike" cells can be induced by E-cadherin molecules [2, 3]. In normal adherent cells such as endothelial (vascular endothelial cadherin, called VE-Cadherin) and epithelial cells (epithelial cadherin, called E-cadherin) cadherins connect two or more cells in a "zipper" like fashion in presence of calcium [1–3, 11]. Importantly, calcium prevents the degradation of cadherin and promotes cell adhesion activity . Cadherin may also be important for mediating "contact-inhibition", a property of normal adherent cells. In a nutshell, Dr. Takeichi observed and described calcium-dependent and -independent mechanisms of cell adhesion .
Short-term incubation of adherent cells with trypsin can digest most ECM molecules and addition of EDTA helps disrupt interactions of cell adhesion mediated by integrins . Dr. Ruoslahti described purification and characterization of fibronectin from blood plasma, and went onto identify the Arg-Gly-Asp (RGD) tri-peptide cell adhesion motif, that remains as a conceptual breakthrough [7, 12]. Structurally, the fibronectin represents a prototypic ECM molecule that displays highly modular structure . Fibronectin possesses repeating structural motifs, classified as fibronectin repeats FN-I, FN-II, and FN-III that are grouped together into functional domains [12, 13]. Many cell types secrete fibronectin polypeptide ranging between 220–250 kDa sizes. Functionally, fibronectin plays critical roles in cell adhesion-dependent cellular activities both in development and adult tissue homeostasis, proliferation, and migration [12, 13]. Cell adhesion assays provided evidence that cell attachment mediated by specific subset of integrins onto fibronectin can be blocked by RGD tri-peptides. Subsequently, many laboratories around the world have also cloned, characterized and described ECM proteins that also may contain RGD or variant cell binding sites. Detergent solubilized plasma-membrane proteins passed through a column chromatography conjugated to RGD-peptides allowed purification of RGD-binding cell adhesion receptors, which is now known as integrins . For detail, please see the RGD story by E. Ruoslahti . Secreted fibronectin can organize and assemble large protein complex by interacting with many other ECM molecules in the extracellular space such as the fibrinogen and collagens, glycosaminoglycans, proteoglycans, tenascin, fibulin and thrombospondin. Many normal cells have been described as "anchorage-dependent" cells that require attachment factor such as fibronectin, without which cells die of apoptosis [15, 16]. Apart from just being a structural support, Fibronectin can trap or sequester growth factors and cytokines, and induce signaling activities [16, 17]. In contrast, neoplastic cells that accumulate mutant copies of genetic materials no longer require fibronectin to grow, divide or metastasize, and this phenomena is called "anchorage-independence". Fibronectin also interacts with bacterial adhesion molecules, a pathological process that helps bacteria to colonize and infect host tissues .
In addition to providing structural support, both cadherins and fibronectin molecules are also required for cell polarity, and informing the cells and tissues about their position in time and space, called positional cues . A biological process that allow cells to sense their immediate physical and chemical environment correctly, for example, to help cells sense presence of glucose and insulin, cytokines and growth hormones, signaling molecules and metal ions. However, such regulatory mechanisms could be altered in many pathological states including tumor growth, angiogenesis and metastasis. Complete understanding of the mechanisms of regulation of cell-adhesion molecules and their signaling activities remains an active area of investigation in many disease settings including cardiovascular, cancer, neural networks, damage and repair mechanisms associated with traumatic injury, wound healing, host-pathogen interactions, nanotechnology, tissue engineering, and molecular therapeutics. The Japan Prize 2005 and cash award is slated to be given in presence of the Emperor of Japan in a week-long celebration beginning 20th April, 2005 http://www.japanprize.jp/English.htm.
The field of cell adhesion is somewhat matured. I apologize to my colleagues and authors whose works could not be cited here due to space constrains. KKW is a recipient of an award from American Heart Association (National Council) and a member of Mission Connect, TIRR, Houston, Texas, and a member of Cardiovascular Research Institute (CVRI) of the Texas A & M University-System Health Science Center.
- Takeichi M: Functional correlation between cell adhesive properties and some cell surface proteins. J Cell Biol. 1977, 75: 464-474. 10.1083/jcb.75.2.464.View ArticlePubMedGoogle Scholar
- Takeichi M: The cadherins: cell-cell adhesion molecules controlling animal morphogenesis. Development. 1988, 102: 639-655.PubMedGoogle Scholar
- Takeichi M: Cadherin cell adhesion receptors as a morphogenetic regulator. Science. 1991, 251: 1451-1455.View ArticlePubMedGoogle Scholar
- Gumbiner BM: Epithelial morphogenesis. Cell. 1992, 69: 385-387. 10.1016/0092-8674(92)90440-N.View ArticlePubMedGoogle Scholar
- Gumbiner BM: Cell adhesion: the molecular basis of tissue architecture and morphogenesis. Cell. 1996, 84: 345-357. 10.1016/S0092-8674(00)81279-9.View ArticlePubMedGoogle Scholar
- Takeichi M: Cadherins in cancer: implications for invasion and metastasis. Curr Opin Cell Biol. 1993, 5: 806-811. 10.1016/0955-0674(93)90029-P.View ArticlePubMedGoogle Scholar
- Ruoslahti E: Fibronectin in cell adhesion and invasion. Cancer Metastasis Rev. 1984, 3: 43-51. 10.1007/BF00047692.View ArticlePubMedGoogle Scholar
- Hynes RO: Integrins: versatility, modulation, and signaling in cell adhesion. Cell. 1992, 69: 11-25. 10.1016/0092-8674(92)90115-S.View ArticlePubMedGoogle Scholar
- Springer TA: Traffic signals for lymphocyte recirculation and leukocyte emigration: The multistep paradigm. Cell. 1994, 76: 301-314. 10.1016/0092-8674(94)90337-9.View ArticlePubMedGoogle Scholar
- Hynes RO, Bader BL: Targeted mutations in integrins and their ligands: their implications for vascular biology. Thromb Haemost. 1997, 78: 83-87.PubMedGoogle Scholar
- Vasioukhin V, Bauer C, Yin M, Fuchs E: Directed actin polymerization is the driving force for epithelial cell-cell adhesion. Cell. 2000, 100: 209-219. 10.1016/S0092-8674(00)81559-7.View ArticlePubMedGoogle Scholar
- Ruoslahti E, Pierschbacher MD: New perspectives in cell adhesion: RGD and integrins. Science. 1987, 238: 491-497.View ArticlePubMedGoogle Scholar
- Yamada KM: Fibronectins: structure, functions and receptors. Curr Opin Cell Biol. 1989, 1: 956-963. 10.1016/0955-0674(89)90065-3.View ArticlePubMedGoogle Scholar
- Ruoslahti E: The RGD story: a personal account. Matrix Biol. 2003, 22: 459-465. 10.1016/S0945-053X(03)00083-0.View ArticlePubMedGoogle Scholar
- Ruoslahti E, Reed JC: Anchorage dependence, integrins, and apoptosis. Cell. 1994, 77: 477-478. 10.1016/0092-8674(94)90209-7.View ArticlePubMedGoogle Scholar
- Giancotti FG, Ruoslahti E: Integrin signaling. Science . 1999, 285: 1028-1032. 10.1126/science.285.5430.1028.View ArticlePubMedGoogle Scholar
- Giancotti FG, Tarone G: Positional control of cell fate through joint integrin/receptor protein kinase signaling. Annu Rev Cell Dev Biol. 2003, 19: 173-206. 10.1146/annurev.cellbio.19.031103.133334.View ArticlePubMedGoogle Scholar
- Patti JM, Allen BL, McGavin MJ, Höök M: MSCRAMM-mediated adherence of microorganisms to host tissues. Annu Rev Microbiol. 1994, 48: 585-617. 10.1146/annurev.mi.48.100194.003101.View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.