Role of the extracellular matrix in morphogenesis

Current Opinion in Biotechnology

Volumn 14, Issue 5, 2003, Pages 526-532

  Kleinman, Hynda K ^a   Philp, Deborah ^a   Hoffman, Matthew P ^a  

^a NATIONAL INSTITUTE OF DENTAL AND CRANIOFACIAL RESEARCH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL ADHESION MOLECULE; CHEMOKINE; COLLAGEN; CYTOKINE; GROWTH FACTOR; LAMININ; PHOSPHATIDYLINOSITOL 3 KINASE; PROTEOGLYCAN;

ANGIOGENESIS; CELL DIFFERENTIATION; CELL PROLIFERATION; EXTRACELLULAR MATRIX; GENE MUTATION; GENE TARGETING; GENETIC CODE; GENETIC DISORDER; HUMAN; MORPHOGENESIS; NONHUMAN; ORGANOGENESIS; PRIORITY JOURNAL; REVIEW; STEM CELL; TISSUE DIFFERENTIATION; TISSUE ENGINEERING; TISSUE INJURY; TISSUE REGENERATION; TISSUE REPAIR;

EID: 0142122297     PISSN: 09581669     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.copbio.2003.08.002     Document Type: Review

References (47)

1. Aumailley M., Gayraud B. Structure and biological activity of extracellular matrix. J. Mol. Med. 76:1998;253-265.
2. Streuli C. Extracellular matrix remodeling and cellular differentiation. Curr. Opin. Cell Biol. 11:1999;634-640.
3. Hohenester H., Engel J. Domain structure and organization of extracellular matrix proteins. Matrix Biol. 21:2002;115-128 This review focuses on the structural requirements important in ECM protein interactions.
4. Mascarenhas J.B., Ruegg M.A., Winzen U., Halfter W., Engel J., Stetefeld J. Mapping of the laminin-binding site of the N-terminal agrin domain(NtA). EMBO J. 22:2003;529-536.
5. Cukierman E., Pankov R., Yamada K.M. Cell interactions with three-dimensional matrices. Curr. Opin. Cell Biol. 14:2002;633-639 This review describes exciting new advances in cell-matrix interactions and focuses on cell shape and signaling events.
6. Ingber D.E. Mechanical signaling and the cellular response to extracellular matrix in angiogenesis and cardiovascular physiology. Circ. Res. 91:2002;877-887 This review describes work on the cell shape, cytoskeleton and cell function.
7. Ponce M.L., Kleinman H.K. Identification of redundant angiogenic sites in laminin α1 and γ1 chains. Exp. Cell Res. 285:2003;189-195.
8. Schenk S., Hintermann E., Bilban M., Koshikawa N., Hojilla C., Khpkha R., Quaranta V. Binding to EGF receptor of a laminin-5 EGF-like fragment liberated during MMP-dependent mammary gland involution. J. Cell Biol. 161:2003;197-209 This is an interesting in vivo demonstration of the role of proteases in releasing active cryptic sites from laminin.
9. Akulapalli S., Sugimoto H., Yang C., Lively J., Zeisberg M., Kalluri R. Human tumistatin and human endostatin exhibit distinct antiangiogenic activities mediated by αvβ3 and α5β1 integrins. Proc. Natl. Acad. Sci. USA. 100:2003;4766-4771.
10. Bokel C., Brown N.H. Integrins in development: moving on, responding to, and sticking to the extracellular matrix. Dev. Cell. 3:2002;311-321 This review provides an update on the integrin receptors and their interactions with the ECM molecules.
11. Gustafsson E., Fassler R. Insights into extracellular matrix functions from mutant mouse models. Exp. Cell Res. 261:2000;52-68.
12. Colognato H., Yurchenco P.D. Form and function: the laminin family of heterotrimers. Dev. Dyn. 218:2000;213-234.
13. Kramerova I.A., Kramerov A.A., Fessler J.H. Alternative splicing of papilin and the diversity of drosophila extracellular matrix during embryonic morphogenesis. Dev. Dyn. 226:2003;634-642.
14. Shimizu H., Zhang X., Zhang J., Leontovich A., Fei K., Yan L., Sarras M.P. Epithelial morphogenesis in hydra requires de novo expression of extracellular matrix components and matrix metalloproteinases. Development. 129:2002;1521-1532.
15. Li S., Harrison D., Carbonetto S., Fassler R., Smyth N., Edgar D., Yurchenco P.D. Matrix assembly, regulation, and survival functions of laminin and its receptors in embryonic stem cell differentiation. J. Cell Biol. 157:2002;1279-1290 This study used knockout mice to define the role of laminin structures and functions in very early development.
16. Akirawa-Hirasawa E., Le A.H., Nonaka I., Ho N.C., Francomano C.A., Govindraj P., Hassell J.H., Devaney J.M., Spranger J., Stevenson R.E.et al. Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonoic myopathy and chondrodysplasia. Am. J. Hum. Genet. 70:2002;1368-1375 This paper summarizes earlier reports of the unexpected finding that perlecan knockout mice have cartilage defects. This finding defined several human genetic diseases involving perlecan mutations.
17. Czyz J., Wobus A.M. Embryonic stem cell differentiation: the role of extracellular factors. Differentiation. 68:2001;167-174.
18. Xu C., Inokuma M.S., Denham J., Golds K., Kundu P., Gold J.D., Carpenter M.K. Feeder-free growth of undifferentiated human embryonic stem cells. Nat. Biotechnol. 19:2001;971-974.
19. Schwartz R.E., Reyes M., Koodie L., Jiang Y., Blackstad M., Lund T., Lenvik T., Johnson S., Hu W.-S., Verfaillie C.M. Multipotent adult progenitor cells from bone marrow differentiate into functional hepatocyte-like cells. J. Clin. Invest. 109:2002;1291-1302.
20. Daniel O.T., Abrahamson D. Endothelial signal integration in vascular assembly. Annu. Rev. Physiol. 62:2000;649-671.
21. Stupack D.G., Cheresh D.A. ECM remodeling regulates angiogenesis: endothelial integrins look for new ligands. Sci. STKE. 2002:2002;PE7.
22. Davis G.E., Bayless K.J., Mavil A. Molecular basis of endothelial cell morphogenesis in three-dimensional extracellular matrices. Anat. Rec. 268:2002;252-275 An excellent review of the interactions of endothelial cells with the ECM, cellular receptors and signaling events.
23. Hogan B.L.M., Kolodziej P.A. Organogenesis: molecular mechanisms of tubulogenesis. Nat. Rev. Genet. 3:2002;513-523.
24. Lubasrksy B., Krasnow M.A. Tube morphogenesis: making and shaping biological tubes. Cell. 112:2003;19-28.
25. Whelan M.C., Senger D.R. Collagen I initiates endothelial cell morphogenesis by inducing actin polymerization through suppression of cyclic AMP and protein kinase A. J. Biol. Chem. 278:2003;327-334.
26. Sanz L., Garcia-Bermejo L., Blanco F.J., Kristensen P., Feijoo M., Suarez E., Blanco B., Alvarez-Vallina L. A novel binding site in the coiled-coil domain of laminin involved in capillary morphogenesis. EMBO J. 22:2003;1508-1517.
27. Ponce M.L., Nomizu M., Kleinman H.K. An angiogenic laminin site and its antagonist bind through the αvβ3 and α5β1 integrins. FASEB J. 15:2001;1389-1397.
28. Gonzalez A.M., Gonzalez M., Herron G.S., Nagavarapu W., Hopkinson S.B., Tsuruta D., Jones J.C.R. Complex interactions between the laminin α4 subunit and integrins regulate endothelial cell behavior in vitro and angiogenesis in vivo. Proc. Natl. Acad Sci. USA. 99:2002;16075-16080.
29. Javaherian K., Park S.Y., Pickl W.F., LaMontagne K.R., Sjin R.T.T., Gillies S., Lo K.-M. Laminin modulates morphogenic properties of collagen XVIII endostatin domain. J. Biol. Chem. 277:2002;45211-45218.
30. Kanda S., Mochizuki Y., Suematsu T., Miyata Y., Nomata K., Kanetake H. Sonic hedgehog induces capillary morphogenesis by endothelial cells through phosphoinositide 3-kinase. J. Biol. Chem. 278:2003;8244-8249.
31. Ruhrberg C., Gerhardt H., Golding M., Watson R., Ioannidou S., Fujisawa H., Betsholts C., Shima D.T. Spatially restricted patterning cues provided by heparin-binding VEGF-A control blood vessel branching morphogenesis. Genes Dev. 16:2002;2684-2698.
32. Salvucci O., Yao L., Villalba S., Sajewicz S., Pittaluga S., Tosato G. Regulation of endothelial cell branching morphogenesis by endogenous chemokine stromal-derived factor-1. Blood. 99:2002;2703-2711.
33. Davies J.A. Do different branching epithelial use a conserved developmental mechanism? Bioessays. 24:2002;937-948 This review discusses the common events involved in branching morphogenesis of several organs.
34. Hoffman M.P., Kidder B., Lakhani S., Steinberg Z., Ho S., Kleinman H., Larsen M. Gene expression profiles of mouse salivary gland development: identification of an important role for FGFR1 signaling and FGF7 and FGF10 expression during salivary gland branching morphogenesis in vitro. Development. 129:2002;5767-5778 The genes expressed during salivary gland development are profiled and the FGF receptors and ligands are shown to have functional importance in gland development.
35. Sakai T., Larsen M., Yamada K.M. Fibronectin requirement in branching morphogenesis. Nature. 423:2003;876-881.
36. Larsen M., Hoffman M.P., Sakai T., Neibaur J.C., Mitchell J.M., Yamada K.M. Role of PI-3 kinase and PIP3 in submandibular gland branching morphogenesis. Dev. Biol. 255:2003;178-191.
37. Hosokawa Y., Takahashi Y., Kadoya Y., Yamashina S., Nomizu M., Yamada Y., Nogawa H. Significant role of laminin-1 in branching morphogenesis of mouse salivary epithelium cultured in basement membrane matrix. Dev. Growth Differ. 41:1999;207-216.
38. Willem M., Miosge N., Halfter W., Smyth N., Jannetti I., Burghart E., Timl R., Maye U. Specific ablation of the nidogen-binding site in the laminin γ1 chain interferes with kidney and lung development. Development. 129:2002;2711-2722.
39. Dong L., Chen Y., Lewis M., Hsieh J.-C., Reing J., Chaillet J.R., Howell C.Y., Melhem M., Inoue S., Kuszak J.R.et al. Neurologic defect and selective disruption of basement membranes in mice lacking entactin-1/nidogen-1. Lab. Invest. 82:2002;1617-1630.
40. Durbeej M., Talts J.F., Henry M.D., Yurchenco P.D., Campbell K.P., Ekblom P. Dystroglycan binding to laminin α1 LG4 module influences epithelial morphogenesis of salivary gland and lung in vitro. Differentiation. 69:2001;121-134.
41. Nguyen N.M., Miner J.H., Pierce R.A., Senior R.M. Laminin α5 is required for lobular septation and visceral pleural basement membrane formation in the developing mouse lung. Dev. Biol. 246:2002;231-244.
42. Weaver V.M., Lelievre S., Lakins J.N., Chrenek M.A., Jones J.C.R., Giancotti F., Werb Z., Bissell M.J. β4 integrin-dependent formation of polarized three-dimensional architecture confers resistance to apoptosis in normal and malignant mammary epithelium. Cancer Cell. 2:2002;205-216.
43. Hoffman M.P., Engbring J.A., Nielsen P., Vargas J., Steinberg Z., Karmand A.J., Nomizu M., Yamada Y., Kleinman H.K. Cell type-specific differences in glycosaminoglycans modulate the biological activity of a heparin-binding peptide (RKRLQVQLSIRT) from the G-domain of the laminin α1 chain. J. Biol. Chem. 276:2001;22077-22085.
44. Badylak S.F. The extracellular matrix as a scaffold for tissue reconstruction. Cell Dev. Biol. 13:2002;377-383.
45. Patel N., Padera R., Sanders G.H.W., Gannizzaro S.M., Davies M.C., Langer R., Roberts C.J., Tendler S.J.B., Williams P.M., Shakeesheff K.M. Spatially controlled cell engineering on biodegradable polymer surfaces. FASEB J. 12:1998;1447-1454.
46. Mochizuki M, Kadoya Y, Wakabayasgi Y, Kato K, Okazaki I, Yamada M, Sato T, Sakairi N, Nishi N, Nomizu M: Laminin-1 peptide-conjugated chitosan membranes as a novel approach for cell engineering. FASEB J 2003: in press.
47. Mann B.K., West J.L. Cell adhesion peptides alter smooth muscle cell adhesion, proliferation, migration, and matrix protein synthesis on modified surface and in polymer scaffolds. J. Biomed. Mater. Res. 60:2002;86-93.