Abstract
The assembly of fibronectin (FN) into a fibrillar matrix is a complex stepwise process that involves binding to integrin receptors as well as interactions between FN molecules. To follow the progression of matrix formation and determine the stages during which specific domains function, we have developed cell lines that lack an endogenous FN matrix but will form fibrils when provided with exogenous FN. Recombinant FNs (recFN) containing deletions of either the RGD cell- binding sequence (RGD-) or the first type III repeats (FN delta III1-7) including the III1 FN binding site were generated with the baculovirus insect cell expression system. After addition to cells, recFN matrix assembly was monitored by indirect immunofluorescence and by insolubility in the detergent deoxycholate (DOC). In the absence of any native FN, FN delta III1-7 was assembled into fibrils and was converted into DOC-insoluble matrix. This process could be inhibited by the amino- terminal 70 kD fragment of FN, showing that FN delta III1-7 follows an assembly pathway similar to FN. The progression of FN delta III1-7 assembly differed from native FN in that the recFN became DOC-insoluble more quickly. In contrast, RGD- recFNs were not formed into fibrils except when added in combination with native FN. These results show that the RGD sequence is essential for the initiation step but fibrils can form independently of the III1-7 modules. The altered rate of FN delta III1-7 assembly suggests that one function of the missing repeats might be to modulate an early stage of matrix formation.
Full Text
The Full Text of this article is available as a PDF (2.6 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Aguirre K. M., McCormick R. J., Schwarzbauer J. E. Fibronectin self-association is mediated by complementary sites within the amino-terminal one-third of the molecule. J Biol Chem. 1994 Nov 11;269(45):27863–27868. [PubMed] [Google Scholar]
- Akiyama S. K., Yamada S. S., Chen W. T., Yamada K. M. Analysis of fibronectin receptor function with monoclonal antibodies: roles in cell adhesion, migration, matrix assembly, and cytoskeletal organization. J Cell Biol. 1989 Aug;109(2):863–875. doi: 10.1083/jcb.109.2.863. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brown P. J., Juliano R. L. Selective inhibition of fibronectin-mediated cell adhesion by monoclonal antibodies to a cell-surface glycoprotein. Science. 1985 Jun 21;228(4706):1448–1451. doi: 10.1126/science.4012302. [DOI] [PubMed] [Google Scholar]
- Busk M., Pytela R., Sheppard D. Characterization of the integrin alpha v beta 6 as a fibronectin-binding protein. J Biol Chem. 1992 Mar 25;267(9):5790–5796. [PubMed] [Google Scholar]
- Castle A. M., Schwarzbauer J. E., Wright R. L., Castle J. D. Differential targeting of recombinant fibronectins in AtT-20 cells based on their efficiency of aggregation. J Cell Sci. 1995 Dec;108(Pt 12):3827–3837. doi: 10.1242/jcs.108.12.3827. [DOI] [PubMed] [Google Scholar]
- Chernousov M. A., Faerman A. I., Frid M. G., Printseva OYu, Koteliansky V. E. Monoclonal antibody to fibronectin which inhibits extracellular matrix assembly. FEBS Lett. 1987 Jun 8;217(1):124–128. doi: 10.1016/0014-5793(87)81255-3. [DOI] [PubMed] [Google Scholar]
- Chernousov M. A., Fogerty F. J., Koteliansky V. E., Mosher D. F. Role of the I-9 and III-1 modules of fibronectin in formation of an extracellular fibronectin matrix. J Biol Chem. 1991 Jun 15;266(17):10851–10858. [PubMed] [Google Scholar]
- Choi M. G., Hynes R. O. Biosynthesis and processing of fibronectin in NIL.8 hamster cells. J Biol Chem. 1979 Dec 10;254(23):12050–12055. [PubMed] [Google Scholar]
- Darribère T., Guida K., Larjava H., Johnson K. E., Yamada K. M., Thiery J. P., Boucaut J. C. In vivo analyses of integrin beta 1 subunit function in fibronectin matrix assembly. J Cell Biol. 1990 May;110(5):1813–1823. doi: 10.1083/jcb.110.5.1813. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Darribère T., Koteliansky V. E., Chernousov M. A., Akiyama S. K., Yamada K. M., Thiery J. P., Boucaut J. C. Distinct regions of human fibronectin are essential for fibril assembly in an in vivo developing system. Dev Dyn. 1992 May;194(1):63–70. doi: 10.1002/aja.1001940108. [DOI] [PubMed] [Google Scholar]
- Engvall E., Ruoslahti E. Binding of soluble form of fibroblast surface protein, fibronectin, to collagen. Int J Cancer. 1977 Jul 15;20(1):1–5. doi: 10.1002/ijc.2910200102. [DOI] [PubMed] [Google Scholar]
- Faull R. J., Kovach N. L., Harlan J. M., Ginsberg M. H. Affinity modulation of integrin alpha 5 beta 1: regulation of the functional response by soluble fibronectin. J Cell Biol. 1993 Apr;121(1):155–162. doi: 10.1083/jcb.121.1.155. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fogerty F. J., Akiyama S. K., Yamada K. M., Mosher D. F. Inhibition of binding of fibronectin to matrix assembly sites by anti-integrin (alpha 5 beta 1) antibodies. J Cell Biol. 1990 Aug;111(2):699–708. doi: 10.1083/jcb.111.2.699. [DOI] [PMC free article] [PubMed] [Google Scholar]
- George E. L., Georges-Labouesse E. N., Patel-King R. S., Rayburn H., Hynes R. O. Defects in mesoderm, neural tube and vascular development in mouse embryos lacking fibronectin. Development. 1993 Dec;119(4):1079–1091. doi: 10.1242/dev.119.4.1079. [DOI] [PubMed] [Google Scholar]
- Giancotti F. G., Ruoslahti E. Elevated levels of the alpha 5 beta 1 fibronectin receptor suppress the transformed phenotype of Chinese hamster ovary cells. Cell. 1990 Mar 9;60(5):849–859. doi: 10.1016/0092-8674(90)90098-y. [DOI] [PubMed] [Google Scholar]
- Ginsberg M. H., Du X., Plow E. F. Inside-out integrin signalling. Curr Opin Cell Biol. 1992 Oct;4(5):766–771. doi: 10.1016/0955-0674(92)90099-x. [DOI] [PubMed] [Google Scholar]
- Hocking D. C., Sottile J., McKeown-Longo P. J. Fibronectin's III-1 module contains a conformation-dependent binding site for the amino-terminal region of fibronectin. J Biol Chem. 1994 Jul 22;269(29):19183–19187. [PubMed] [Google Scholar]
- Hynes R. O., Destree A. Extensive disulfide bonding at the mammalian cell surface. Proc Natl Acad Sci U S A. 1977 Jul;74(7):2855–2859. doi: 10.1073/pnas.74.7.2855. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hynes R. O., George E. L., Georges E. N., Guan J. L., Rayburn H., Yang J. T. Toward a genetic analysis of cell-matrix adhesion. Cold Spring Harb Symp Quant Biol. 1992;57:249–258. doi: 10.1101/sqb.1992.057.01.030. [DOI] [PubMed] [Google Scholar]
- Keski-Oja J., Mosher D. F., Vaheri A. Dimeric character of fibronectin, a major cell surface-associated glycoprotein. Biochem Biophys Res Commun. 1977 Jan 24;74(2):699–706. doi: 10.1016/0006-291x(77)90359-x. [DOI] [PubMed] [Google Scholar]
- Lin A. Y., Devaux B., Green A., Sagerström C., Elliott J. F., Davis M. M. Expression of T cell antigen receptor heterodimers in a lipid-linked form. Science. 1990 Aug 10;249(4969):677–679. doi: 10.1126/science.1696397. [DOI] [PubMed] [Google Scholar]
- Marcantonio E. E., Hynes R. O. Antibodies to the conserved cytoplasmic domain of the integrin beta 1 subunit react with proteins in vertebrates, invertebrates, and fungi. J Cell Biol. 1988 May;106(5):1765–1772. doi: 10.1083/jcb.106.5.1765. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McDonald J. A. Extracellular matrix assembly. Annu Rev Cell Biol. 1988;4:183–207. doi: 10.1146/annurev.cb.04.110188.001151. [DOI] [PubMed] [Google Scholar]
- McDonald J. A., Quade B. J., Broekelmann T. J., LaChance R., Forsman K., Hasegawa E., Akiyama S. Fibronectin's cell-adhesive domain and an amino-terminal matrix assembly domain participate in its assembly into fibroblast pericellular matrix. J Biol Chem. 1987 Mar 5;262(7):2957–2967. [PubMed] [Google Scholar]
- McKeown-Longo P. J., Mosher D. F. Binding of plasma fibronectin to cell layers of human skin fibroblasts. J Cell Biol. 1983 Aug;97(2):466–472. doi: 10.1083/jcb.97.2.466. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McKeown-Longo P. J., Mosher D. F. Interaction of the 70,000-mol-wt amino-terminal fragment of fibronectin with the matrix-assembly receptor of fibroblasts. J Cell Biol. 1985 Feb;100(2):364–374. doi: 10.1083/jcb.100.2.364. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Merril C. R., Goldman D., Van Keuren M. L. Gel protein stains: silver stain. Methods Enzymol. 1984;104:441–447. doi: 10.1016/s0076-6879(84)04111-2. [DOI] [PubMed] [Google Scholar]
- Morla A., Ruoslahti E. A fibronectin self-assembly site involved in fibronectin matrix assembly: reconstruction in a synthetic peptide. J Cell Biol. 1992 Jul;118(2):421–429. doi: 10.1083/jcb.118.2.421. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Morla A., Zhang Z., Ruoslahti E. Superfibronectin is a functionally distinct form of fibronectin. Nature. 1994 Jan 13;367(6459):193–196. doi: 10.1038/367193a0. [DOI] [PubMed] [Google Scholar]
- Mosher D. F., Sottile J., Wu C., McDonald J. A. Assembly of extracellular matrix. Curr Opin Cell Biol. 1992 Oct;4(5):810–818. doi: 10.1016/0955-0674(92)90104-k. [DOI] [PubMed] [Google Scholar]
- Quade B. J., McDonald J. A. Fibronectin's amino-terminal matrix assembly site is located within the 29-kDa amino-terminal domain containing five type I repeats. J Biol Chem. 1988 Dec 25;263(36):19602–19609. [PubMed] [Google Scholar]
- Roman J., LaChance R. M., Broekelmann T. J., Kennedy C. J., Wayner E. A., Carter W. G., McDonald J. A. The fibronectin receptor is organized by extracellular matrix fibronectin: implications for oncogenic transformation and for cell recognition of fibronectin matrices. J Cell Biol. 1989 Jun;108(6):2529–2543. doi: 10.1083/jcb.108.6.2529. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schwarzbauer J. E. Identification of the fibronectin sequences required for assembly of a fibrillar matrix. J Cell Biol. 1991 Jun;113(6):1463–1473. doi: 10.1083/jcb.113.6.1463. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schwarzbauer J. E., Spencer C. S., Wilson C. L. Selective secretion of alternatively spliced fibronectin variants. J Cell Biol. 1989 Dec;109(6 Pt 2):3445–3453. doi: 10.1083/jcb.109.6.3445. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sottile J., Wiley S. Assembly of amino-terminal fibronectin dimers into the extracellular matrix. J Biol Chem. 1994 Jun 24;269(25):17192–17198. [PubMed] [Google Scholar]
- Wennerberg K., Lohikangas L., Gullberg D., Pfaff M., Johansson S., Fässler R. Beta 1 integrin-dependent and -independent polymerization of fibronectin. J Cell Biol. 1996 Jan;132(1-2):227–238. doi: 10.1083/jcb.132.1.227. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wu C., Bauer J. S., Juliano R. L., McDonald J. A. The alpha 5 beta 1 integrin fibronectin receptor, but not the alpha 5 cytoplasmic domain, functions in an early and essential step in fibronectin matrix assembly. J Biol Chem. 1993 Oct 15;268(29):21883–21888. [PubMed] [Google Scholar]
- Wu C., Chung A. E., McDonald J. A. A novel role for alpha 3 beta 1 integrins in extracellular matrix assembly. J Cell Sci. 1995 Jun;108(Pt 6):2511–2523. doi: 10.1242/jcs.108.6.2511. [DOI] [PubMed] [Google Scholar]
- Wu C., Fields A. J., Kapteijn B. A., McDonald J. A. The role of alpha 4 beta 1 integrin in cell motility and fibronectin matrix assembly. J Cell Sci. 1995 Feb;108(Pt 2):821–829. doi: 10.1242/jcs.108.2.821. [DOI] [PubMed] [Google Scholar]
- Wu C., Keivens V. M., O'Toole T. E., McDonald J. A., Ginsberg M. H. Integrin activation and cytoskeletal interaction are essential for the assembly of a fibronectin matrix. Cell. 1995 Dec 1;83(5):715–724. doi: 10.1016/0092-8674(95)90184-1. [DOI] [PubMed] [Google Scholar]
- Yang J. T., Rayburn H., Hynes R. O. Embryonic mesodermal defects in alpha 5 integrin-deficient mice. Development. 1993 Dec;119(4):1093–1105. doi: 10.1242/dev.119.4.1093. [DOI] [PubMed] [Google Scholar]
- Zhang Q., Checovich W. J., Peters D. M., Albrecht R. M., Mosher D. F. Modulation of cell surface fibronectin assembly sites by lysophosphatidic acid. J Cell Biol. 1994 Dec;127(5):1447–1459. doi: 10.1083/jcb.127.5.1447. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zhang Z., Morla A. O., Vuori K., Bauer J. S., Juliano R. L., Ruoslahti E. The alpha v beta 1 integrin functions as a fibronectin receptor but does not support fibronectin matrix assembly and cell migration on fibronectin. J Cell Biol. 1993 Jul;122(1):235–242. doi: 10.1083/jcb.122.1.235. [DOI] [PMC free article] [PubMed] [Google Scholar]