This Article Full Text Full Text (PDF) Data Supplement All Versions of this Article: 105/3/214    most recent CIRCRESAHA.109.199984v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Request Permissions Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Martin, K. Articles by Caplice, N. Search for Related Content PubMed PubMed Citation Articles by Martin, K. Articles by Caplice, N. Related Collections Smooth muscle proliferation and differentiation Thrombin Other Vascular biology

(Circulation Research. 2009;105:214.)
© 2009 American Heart Association, Inc.

Reports

Thrombin Stimulates Smooth Muscle Cell Differentiation From Peripheral Blood Mononuclear Cells via Protease-Activated Receptor-1, RhoA, and Myocardin

Kenneth Martin^*, Sharon Weiss^*, Pat Metharom, Jeffrey Schmeckpeper, Brian Hynes, John O'Sullivan, Noel Caplice

From the Centre for Research in Vascular Biology, Biosciences Institute, University College Cork, Ireland.

Correspondence to Noel Caplice, MD, PhD, Rm 2.39, CRVB, Biosciences Institute, University College Cork, Cork, Ireland. E-mail n.caplice{at}ucc.ie

Abstract

Rationale: Smooth muscle precursor cells have previously been reported to reside in bone marrow and in the circulation, but little is currently known regarding the proximate stimuli for smooth muscle cell differentiation of these putative progenitors.

Objective: Because local thrombin generation occurs as an initial response to vascular injury, we hypothesized that thrombin may influence the differentiation of circulating smooth muscle progenitor cells.

Methods and Results: Peripheral blood mononuclear cells were cultured on type I collagen using a protocol optimized to stimulate smooth muscle cell outgrowth. Thrombin-stimulated upregulation of the transcription factor myocardin and smooth muscle myosin heavy chain, and both were inhibited by hirudin or the RhoA inhibitor Y27632. After 10 days of culture, smooth muscle outgrowth colonies formed, which stained positive for -smooth muscle actin, smooth muscle myosin heavy chain, and calponin, in addition to having a contractile response to 100 nmol/L angiotensin II. Coincubation of peripheral blood mononuclear cells with thrombin, 10 µmol/L protease-activated receptor-1, but not protease-activated receptor-4 activating peptide significantly increased the number of smooth muscle outgrowth colonies formed. Thrombin-induced enhancement of smooth muscle outgrowth colony formation was inhibited by hirudin, Y27632, and an antibody against protease-activated receptor-1.

Conclusions: These data illustrate a novel thrombin-induced pathway for smooth muscle differentiation from putative smooth muscle progenitors in peripheral blood.

Key Words: thrombin • RhoA • myocardin • smooth muscle differentiation • circulating progenitor cells