Literature DB >> 7400245

Formation of cell-to-substrate contacts during fibroblast motility: an interference-reflexion study.

C S Izzard, L R Lochner.   

Abstract

The formatin of close contacts and focal contacts (ca. 30 nm and 10-15 nm separation distance respectively) has been studied during the movement of chick heart fibroblasts on planar substrates using interference-reflexion microscopy, and evaluated in the context of spreading and net movement. During spreading the overall advance of the margin of the close contact is steady, punctuated by periods in which it remains stationary, and only 5% of the time is spent withdrawing in contrast to the extreme leading edge. The close contact advances only where a lamellipodium has first extended free of the substrate (greater than or equal to 100 nm separation distance) ahead of the existing close contact. The new close contact is formed by the lamellipodium lowering to the substrate either progressively from its base forward or distally in patches which later join with the main close contact. New focal contacts are formed successively ahead of existing ones, either by microspikes or lamellipodia contacting the substrate locally ahead of the close contact, or within the close contact usually immediately, but not more than 1-2 microns, behind its margin. Examining the cell margin alternately with interference-reflexion and differential-interference contrast showed that the formation of the focal contact was preceded in 90% of the cases by the development of a linear structure in the form of a microspike (as expected), a short projection (< 2 microns long) of the lamellipodium, or a fibre within the lamellipodium, each of which could be traced to the cytoplasmic fibre typically associated with the focal contact. Stress fibres subsequently developed centripetally from these initial fibres. The different forms of the linear structure which preceded the focal contact were interchangeable, giving rise to one another, and we have evaluated that the structure common to each is probably a short bundle of microfilaments. The following features indicate that the close contact plays a primary role in marginal spreading: it is lost when spreading ceases; it is reformed when spreading resumes but only under the newly spread area; the advance of the margin of the thicker leading lamella closely follows that of the close contact; the advance of both can occur ahead of and is thus independent of existing focal contacts and associated stress fibres. We propose that the close contact provides the adhesion required to transmit to the substrate the forces involved in the forward movements of the marginal cytoplasm. The continual formation of focal contacts and stress fibres at the margin is consistent with their role, suggested by others, in drawing the bulk of the cell forward. These evaluations are discussed in the context of the form and distribution of contractile proteins in the cell margin. A primary role of the lamellipodia and microspikes in extending the cell margin and forming new adhesions, preparatory to further cytoplasmic movement, is established by this work.

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Mesh:

Year:  1980        PMID: 7400245     DOI: 10.1242/jcs.42.1.81

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  76 in total

Review 1.  Morphology of cell-substratum adhesion. Influence of receptor heterogeneity and nonspecific forces.

Authors:  M D Ward; D A Hammer
Journal:  Cell Biophys       Date:  1992 Apr-Jun

2.  The control of cellular shape and motility. Mg2+ and tropomyosin regulate the formation and the dissociation of microfilament bundles.

Authors:  E Grazi; P Cuneo; A Cataldi
Journal:  Biochem J       Date:  1992-12-15       Impact factor: 3.857

3.  Electrically excitable normal rat kidney fibroblasts: A new model system for cell-semiconductor hybrids.

Authors:  W J Parak; J Domke; M George; A Kardinal; M Radmacher; H E Gaub; A D de Roos; A P Theuvenet; G Wiegand; E Sackmann; J C Behrends
Journal:  Biophys J       Date:  1999-03       Impact factor: 4.033

4.  Spreading of wheat germ agglutinin-induced erythrocyte contact by formation of spatially discrete contacts.

Authors:  H Darmani; W T Coakley; A C Hann; A Brain
Journal:  Cell Biophys       Date:  1990-06

5.  Impedance analysis of renal vascular smooth muscle cells.

Authors:  Lavanya Balasubramanian; Kay-Pong Yip; Tai-Hsin Hsu; Chun-Min Lo
Journal:  Am J Physiol Cell Physiol       Date:  2008-08-06       Impact factor: 4.249

6.  Micromotion of mammalian cells measured electrically.

Authors:  I Giaever; C R Keese
Journal:  Proc Natl Acad Sci U S A       Date:  1991-09-01       Impact factor: 11.205

7.  Spectrally coded optical nanosectioning (SpecON) with biocompatible metal-dielectric-coated substrates.

Authors:  Kareem Elsayad; Alexander Urich; Piau Siong Tan; Maria Nemethova; J Victor Small; Karl Unterrainer; Katrin G Heinze
Journal:  Proc Natl Acad Sci U S A       Date:  2013-11-25       Impact factor: 11.205

Review 8.  The role of cell adhesion proteins--laminin and fibronectin--in the movement of malignant and metastatic cells.

Authors:  J B McCarthy; M L Basara; S L Palm; D F Sas; L T Furcht
Journal:  Cancer Metastasis Rev       Date:  1985       Impact factor: 9.264

9.  Redistribution of microfilament-associated proteins during the formation of focal contacts and adhesions in chick fibroblasts.

Authors:  J R Couchman; R A Badley; D A Rees
Journal:  J Muscle Res Cell Motil       Date:  1983-12       Impact factor: 2.698

10.  Lymph node metastasis and cell movement: ultrastructural studies on the rat 13762 mammary carcinoma and Walker carcinoma.

Authors:  I Carr; M Levy; K Orr; J Bruni
Journal:  Clin Exp Metastasis       Date:  1985 Apr-Jun       Impact factor: 5.150

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