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PMID: 3623023 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Heparin modulates human intestinal smooth muscle cell proliferation, protein synthesis, and lattice contraction.

Gastroenterology ·Vol. 93 ·No. 4 ·1987-10-00 ·Pages 801-9

Graham MF, Drucker DE, Perr HA, Diegelmann RF, Ehrlich HP

Abstract

The effect of heparin on human intestinal smooth muscle cell proliferation, collagen and noncollagen protein synthesis, and collagen lattice contraction was studied in vitro. Proliferation of serum-stimulated cells was inhibited in a concentration-related fashion by continuous exposure to heparin. The inhibition of proliferation was reversible when heparin was removed from the culture medium. Collagen synthesis was inhibited by 24-h exposure to heparin, but only during that phase of culture (8-12 days) when collagen synthesis was maximal. Noncollagen protein synthesis was down-regulated by 24-h exposure to heparin at all phases of culture tested (5-21 days). Heparin also abolished the contraction of collagen lattices populated by human intestinal smooth muscle cells. These studies demonstrate that heparin plays a significant role in the modulation of human intestinal smooth muscle cell behavior in vitro and suggest that a similar role is played by heparinlike components of the extracellular matrix in vivo.

MeSH Terms
Cell Division Cells, Cultured Collagen/biosynthesis Culture Media Cytoskeleton/drug effects Dose-Response Relationship, Drug Heparin/pharmacology Humans Jejunum/cytology,drug effects,metabolism Muscle, Smooth/drug effects Photomicrography Protein Biosynthesis
Chemicals
Culture Media Heparin Collagen
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Graham M F
Drucker D E
Perr H A
Diegelmann R F
Ehrlich H P
Article Info
Journal
Gastroenterology
Abbr.
Gastroenterology
ISSN
0016-5085
Published
1987-10-00
Pages
801-9
Language
English
Region
United States
NLM ID
0374630
Subset
IM
Grants
NIADDK NIH HHS · AM34151 · United States
NIGMS NIH HHS · GM25561 · United States
NIGMS NIH HHS · GM32707 · United States
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