Migration by haptotaxis of a Schwann cell tumor line to the basement membrane glycoprotein laminin - PubMed (original) (raw)
Migration by haptotaxis of a Schwann cell tumor line to the basement membrane glycoprotein laminin
J B McCarthy et al. J Cell Biol. 1983 Sep.
Abstract
Laminin is a large (greater than 850-kdalton) glycoprotein that is localized within basement membranes. Recent work has indicated that this protein is present within the endoneurium of mouse sciatic nerve. Furthermore, it has been shown that a rat Schwannoma cell line, RN22F, produced laminin and that laminin promoted the attachment of these cells to bacterial plastic. This report presents evidence that RN22F cells migrate in vitro to laminin in a concentration-dependent fashion. Laminin was extracted from the mouse EHS tumor and purified by molecular sieve and heparin-agarose affinity chromatography. The migration of Schwannoma cells to laminin, as assessed in a microwell modified Boyden chamber, was inhibited in a dose-dependent manner by affinity-purified antilaminin antibody. Zigmond-Hirsch checkerboard analysis experiments indicated that laminin stimulated both random and directed movement of RN22F cells. Additionally, reversal of the laminin gradient in the chambers also stimulated RN22F migration in a concentration-dependent manner, suggesting that directed migration of RN22F cells was due to a substratum-bound laminin (haptotaxis) as opposed to cell movement in response to fluid-phase laminin (chemotaxis). Binding studies using [3H]laminin demonstrated that laminin bound to the filter surface under the assay conditions used, and support the contention that cells are migrating to substrate-bound material. Furthermore, RN22F cells were shown to migrate on filters coated with laminin in the absence of additional fluid-phase laminin. The magnitude of this response could be altered by changing the relative density of bound laminin. In contrast, fibronectin promoted only marginal migration of RN22F cells. Collectively, these observations indicate that haptotaxis may be a mechanism by which laminin may guide cells during development and raise the possibility that it may be involved in peripheral nervous system myelination.
Similar articles
- Thrombospondin-induced tumor cell migration: haptotaxis and chemotaxis are mediated by different molecular domains.
Taraboletti G, Roberts DD, Liotta LA. Taraboletti G, et al. J Cell Biol. 1987 Nov;105(5):2409-15. doi: 10.1083/jcb.105.5.2409. J Cell Biol. 1987. PMID: 3680388 Free PMC article. - Production of laminin and fibronectin by Schwannoma cells: cell-protein interactions in vitro and protein localization in peripheral nerve in vivo.
Palm SL, Furcht LT. Palm SL, et al. J Cell Biol. 1983 May;96(5):1218-26. doi: 10.1083/jcb.96.5.1218. J Cell Biol. 1983. PMID: 6341376 Free PMC article. - Laminin and fibronectin promote the haptotactic migration of B16 mouse melanoma cells in vitro.
McCarthy JB, Furcht LT. McCarthy JB, et al. J Cell Biol. 1984 Apr;98(4):1474-80. doi: 10.1083/jcb.98.4.1474. J Cell Biol. 1984. PMID: 6715409 Free PMC article. - Laminin and fibronectin in normal and malignant neuroectodermal cells.
Liesi P. Liesi P. Med Biol. 1984;62(3):163-80. Med Biol. 1984. PMID: 6387323 Review. - Mechanisms of cell migration in the vertebrate embryo.
Thiery JP. Thiery JP. Cell Differ. 1984 Nov;15(1):1-15. doi: 10.1016/0045-6039(84)90024-1. Cell Differ. 1984. PMID: 6394144 Review.
Cited by
- Thrombospondin-induced tumor cell migration: haptotaxis and chemotaxis are mediated by different molecular domains.
Taraboletti G, Roberts DD, Liotta LA. Taraboletti G, et al. J Cell Biol. 1987 Nov;105(5):2409-15. doi: 10.1083/jcb.105.5.2409. J Cell Biol. 1987. PMID: 3680388 Free PMC article. - Type IV collagen and laminin in the synovial intimal layer: an immunohistochemical study.
Pollock LE, Lalor P, Revell PA. Pollock LE, et al. Rheumatol Int. 1990;9(6):277-80. doi: 10.1007/BF00541324. Rheumatol Int. 1990. PMID: 2315607 - Use of a reconstituted basement membrane to measure cell invasiveness and select for highly invasive tumor cells.
Terranova VP, Hujanen ES, Loeb DM, Martin GR, Thornburg L, Glushko V. Terranova VP, et al. Proc Natl Acad Sci U S A. 1986 Jan;83(2):465-9. doi: 10.1073/pnas.83.2.465. Proc Natl Acad Sci U S A. 1986. PMID: 3455782 Free PMC article. - Subcellular spatial segregation of integrin subtypes by patterned multicomponent surfaces.
Desai RA, Khan MK, Gopal SB, Chen CS. Desai RA, et al. Integr Biol (Camb). 2011 May;3(5):560-7. doi: 10.1039/c0ib00129e. Epub 2011 Feb 4. Integr Biol (Camb). 2011. PMID: 21298148 Free PMC article. - Gap geometry dictates epithelial closure efficiency.
Ravasio A, Cheddadi I, Chen T, Pereira T, Ong HT, Bertocchi C, Brugues A, Jacinto A, Kabla AJ, Toyama Y, Trepat X, Gov N, Neves de Almeida L, Ladoux B. Ravasio A, et al. Nat Commun. 2015 Jul 9;6:7683. doi: 10.1038/ncomms8683. Nat Commun. 2015. PMID: 26158873 Free PMC article.
References
- Nature. 1977 Nov 24;270(5635):351-2 - PubMed
- Cell. 1978 Feb;13(2):263-71 - PubMed
- Cell. 1978 Jun;14(2):439-46 - PubMed
- J Cell Biol. 1978 Sep;78(3):943-50 - PubMed
- Exp Cell Res. 1978 Dec;117(2):403-12 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources