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PMID: 2478828 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

The interactions of vascular cells with solid phase (matrix) and soluble factors.

Journal of cardiovascular pharmacology ·Vol. 14 Suppl 6 ·1989-00-00 ·Pages S70-5

Madri JA, Kocher O, Merwin JR, Bell L, Yannariello-Brown J

Abstract

The vessel wall is composed of heterogeneous cell populations residing in a variety of vascular beds. Each cell type has different functions and morphologies but all of them have a role in the repair process following vascular injury. Responses to injury vary depending upon the type and extent of the injury and the vascular bed affected. The sheet migration and proliferation exhibited by large vessel endothelial cells is in striking contrast to the migration through soft tissues and tube formation exhibited by microvascular endothelial cells in response to injury. Vascular smooth muscle cells respond to injury by migrating into the intima, proliferating and synthesizing matrix, causing intimal thickening. The response to injury by vascular cells appears to be modulated, in part, by the composition and organization of the surrounding matrix and the various platelet factors and cytokines found at sites of injury. Furthermore, evidence has been accrued in culture, suggesting that solid phase (matrix) and soluble factors modulate each other's effects on local vascular cell populations following injury.

MeSH Terms
Animals Blood Vessels/cytology Humans Muscle, Smooth, Vascular/cytology,physiology
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Madri J A
Department of Pathology, Yale University, School of Medicine, New Haven, Connecticut 06510.
Kocher O
Merwin J R
Bell L
Yannariello-Brown J
Article Info
Journal
Journal of cardiovascular pharmacology
Abbr.
J Cardiovasc Pharmacol
ISSN
0160-2446
Published
1989-00-00
Pages
S70-5
Language
English
Region
United States
NLM ID
7902492
Subset
IM
Grants
NIDDK NIH HHS · P01-DK38979 · United States
NHLBI NIH HHS · R01-HL28373 · United States
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