The proliferation and differentiation of placental-derived multipotent cells into smooth muscle cells on fibrillar collagen.

Abstract:

:Type I collagen constitutes a major portion of the extracellular matrix (ECM) in arterial wall and it is the major substrate for cell growth and differentiation. The goal of this study was to evaluate the differentiation and proliferation of placenta-derived multipotent cells (PDMCs) on polymerized type I collagen fibrils and monomer collagen. PDMCs grown on both polymerized collagen and monomer collagen with transforming growth factor (TGF)-beta treatment increases the expression of smooth muscle cell (SMC)-specific markers, including calponin, alpha-smooth muscle actin (alpha-SMA) and smooth muscle-myosin heavy chain (SM-MHC). Polymerized collagen increased the expressions of p21(CIP1) and p27(KIP1); decreased cyclin A, cyclin D1, cyclin-dependent protein kinase 2 (Cdk2); and led to G(0)/G(1) arrest in PDMCs. Furthermore, PDMC-differentiated SMCs exhibited significant collagen contractility in the presence or absence of endothelin-1 (ET-1) stimulation. By using specific inhibitors and small interfering RNA (siRNA), we demonstrated that p38 MAPK pathway and serum response factor (SRF)-DNA binding activity is critical for the polymerized collagen-induced PDMC differentiation into SMCs. Thus, polymerized collagen exhibits the great potential in inducing PDMCs differentiation into SMCs, and exerts anti-proliferative effect on PDMC-differentiated SMCs.

journal_name

Biomaterials

journal_title

Biomaterials

authors

Chou MT,Chang SN,Ke C,Chang HI,Sung ML,Kuo HC,Chen CN

doi

10.1016/j.biomaterials.2010.02.011

subject

Has Abstract

pub_date

2010-05-01 00:00:00

pages

4367-75

issue

15

eissn

0142-9612

issn

1878-5905

pii

S0142-9612(10)00224-3

journal_volume

31

pub_type

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