Literature DB >> 6541224

The organization of microfilaments in spreading platelets: a comparison with fibroblasts and glial cells.

R Karlsson, I Lassing, A S Höglund, U Lindberg.   

Abstract

Platelets respond to stimulatory agents in general by the formation of long spikelike surface projections built up of tightly bundled microfilaments. During contact stimulation this is followed by a second phase when thin membrane lamellae grow out between the projections. This behaviour resembles that seen for instance in fibroblasts and glial cells, sending out microspikes and lamellipodia as a step in their advancement over solid substrata. Conditions, designed earlier for the preservation and visualization of the fragile organization of microfilaments and microtubules in the peripheral, highly motile parts (leading lamellae) of such cells (Höglund et al. (1980) J. Musc. Res. Cell Motility, 1:127-146), were used here to produce high-resolution images of the ultrastructural organization of platelets spreading on a solid substratum. This revealed an unexpected arrangement of actin filaments running parallel to the advancing edge, and small tufts of microfilaments on the outside of this edge-bundle. Cytochalasin D caused a regression of the spikelike projections as well as of both types of structures in the advancing platelet lamella and led to the appearance of a dense filamentous mat in juxtaposition to the plasma membrane. Analysis of the actin pools using the DNAase inhibition assay showed that the dramatic reorganizations of actin seen during the two phases of contact stimulation was reflected in a shift in the G/F-actin ratio only during the early phase.

Entities:  

Mesh:

Substances:

Year:  1984        PMID: 6541224     DOI: 10.1002/jcp.1041210113

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  14 in total

1.  2E4 (kaptin): a novel actin-associated protein from human blood platelets found in lamellipodia and the tips of the stereocilia of the inner ear.

Authors:  E L Bearer; M T Abraham
Journal:  Eur J Cell Biol       Date:  1999-02       Impact factor: 4.492

2.  Actin filament organization in aligned prefusion myoblasts.

Authors:  Nathan T Swailes; Peter J Knight; Michelle Peckham
Journal:  J Anat       Date:  2004-11       Impact factor: 2.610

3.  Surface-activated bovine platelets do not spread, they unfold.

Authors:  L H Grouse; G H Rao; D J Weiss; V Perman; J G White
Journal:  Am J Pathol       Date:  1990-02       Impact factor: 4.307

Review 4.  Actin dynamics in platelets.

Authors:  E L Bearer; J M Prakash; Z Li
Journal:  Int Rev Cytol       Date:  2002

5.  Pattern formation and handedness in the cytoskeleton of human platelets.

Authors:  J Hagmann
Journal:  Proc Natl Acad Sci U S A       Date:  1993-04-15       Impact factor: 11.205

6.  Identification of a membrane skeleton in platelets.

Authors:  J E Fox; J K Boyles; M C Berndt; P K Steffen; L K Anderson
Journal:  J Cell Biol       Date:  1988-05       Impact factor: 10.539

7.  Role of the membrane skeleton in preventing the shedding of procoagulant-rich microvesicles from the platelet plasma membrane.

Authors:  J E Fox; C D Austin; J K Boyles; P K Steffen
Journal:  J Cell Biol       Date:  1990-08       Impact factor: 10.539

8.  Actin filament organization in the fish keratocyte lamellipodium.

Authors:  J V Small; M Herzog; K Anderson
Journal:  J Cell Biol       Date:  1995-06       Impact factor: 10.539

9.  Blood platelets are assembled principally at the ends of proplatelet processes produced by differentiated megakaryocytes.

Authors:  J E Italiano; P Lecine; R A Shivdasani; J H Hartwig
Journal:  J Cell Biol       Date:  1999-12-13       Impact factor: 10.539

10.  Mechanisms of actin rearrangements mediating platelet activation.

Authors:  J H Hartwig
Journal:  J Cell Biol       Date:  1992-09       Impact factor: 10.539

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.