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PMID: 2932470 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Linkage of a membrane skeleton to integral membrane glycoproteins in human platelets. Identification of one of the glycoproteins as glycoprotein Ib.

The Journal of clinical investigation ·Vol. 76 ·No. 4 ·1985-10-00 ·Pages 1673-83

Fox JE

Abstract

Experiments were performed to determine whether platelets contain a membrane skeleton. Platelets were labeled by a sodium periodate/sodium [3H]borohydride method and lysed with Triton X-100. Much of the filamentous actin could be sedimented at low g forces (15,600 g, 4 min), but some of the actin filaments required high-speed centrifugation for their sedimentation (100,000 g, 3 h). The latter filaments differed from those in the low-speed pellet in that they could not be depolymerized by Ca2+ and could not be sedimented at low g forces even from Triton X-100 lysates of platelets that had been activated with thrombin. Actin-binding protein sedimented with both types of filaments, but 3H-labeled membrane glycoproteins were recovered mainly with the high-speed filaments. The primary 3H-labeled glycoprotein recovered with this "membrane skeleton" was glycoprotein (GP) Ib. Approximately 70% of the platelet GP Ib was present in this skeleton. Several other minor glycoproteins, including greater than 50% of the GP Ia and small amounts of three unidentified glycoproteins of Mr greater than 200,000, were also recovered with the membrane skeleton. The Triton X-100 insolubility of GP Ib, GP Ia, a minor membrane glycoprotein of 250,000 Mr, and actin-binding protein resulted from their association with actin filaments as they were rendered Triton X-100-soluble when actin filaments were depolymerized with deoxyribonuclease I and co-isolated with actin filaments on sucrose gradients. When isolated platelet plasma membranes were extracted with Triton X-100, actin, actin-binding protein, and GP Ib were recovered as the Triton X-100 residue. These studies show that unstimulated platelets contain a membrane skeleton composed of actin filaments and actin-binding protein that is distinct from the rest of the cytoskeleton and is attached to GP Ib, GP Ia, and a minor glycoprotein of 250,000 Mr on the plasma membrane.

MeSH Terms
Actin Cytoskeleton/analysis Actins/isolation & purification Adult Blood Platelets/analysis,ultrastructure Cell Membrane/analysis,ultrastructure Centrifugation Cytoskeleton/analysis,ultrastructure Deoxyribonuclease I Glycoproteins/isolation & purification Humans Membrane Proteins/isolation & purification Microfilament Proteins/isolation & purification Molecular Weight Octoxynol Platelet Membrane Glycoproteins Polyethylene Glycols Solubility
Chemicals
Actins Glycoproteins Membrane Proteins Microfilament Proteins Platelet Membrane Glycoproteins Polyethylene Glycols Octoxynol Deoxyribonuclease I
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Fox J E
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Article Info
Journal
The Journal of clinical investigation
Abbr.
J Clin Invest
ISSN
0021-9738
Published
1985-10-00
Pages
1673-83
Language
English
Region
United States
NLM ID
7802877
PMCID
PMC424161
Subset
IM
Grants
NHLBI NIH HHS · HL-30657 · United States
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