Literature DB >> 1917792

Isolation of two morphologically distinct cell lines from rat arterial smooth muscle expressing high tumorigenic potentials.

N Blaes1, M C Bourdillon, J M Daniel-Lamaziere, J J Michaille, M Andujar, C Covacho.   

Abstract

Smooth muscle cell proliferation is an important feature of atherogenesis. Some works have hypothesized that a transformation of smooth muscle cells could arise during this pathological process. The present paper describes two spontaneously transformed cell lines of arterial smooth muscle cells (SMC) established from aortic media of adult rat. The cell lines have been designated V6 and V8; some of their morphologic, growth, and metabolic characteristics are described and compared to their parent cells. The two cell lines appeared distinct by their morphology and by their degree of transformation. V6 cells appeared as elongated spindle-shaped cells whereas V8 cells were spread cells with a cobblestone pattern. Karyotypes of both cell lines showed a high polyploidy level. V6 and V8 cell lines were immortalized and showed growth characteristics of transformed cells: low requirement of serum to grow, ability to form colonies in soft agar and tumorigenicity in nude mice; V8 cells presented a higher malignancy than V6 cells. Both V6 and V8 cells exhibited characteristics of cultured arterial SMC: ultrastructure, alpha actin expression at the protein and mRNA level, prostacyclin production. The remarkably different morphologies of the V6 and V8 lines and their transformed phenotype suggest that these cell lines could be useful models to study SMC differentiation and proliferation with respect to atherosclerotic or hypertensive vascular diseases.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1917792     DOI: 10.1007/bf02633218

Source DB:  PubMed          Journal:  In Vitro Cell Dev Biol        ISSN: 0883-8364


  46 in total

1.  Platelet-derived growth factor mRNA detection in human atherosclerotic plaques by in situ hybridization.

Authors:  J N Wilcox; K M Smith; L T Williams; S M Schwartz; D Gordon
Journal:  J Clin Invest       Date:  1988-09       Impact factor: 14.808

2.  Arterial smooth muscle cells in primary culture produce a platelet-derived growth factor-like protein.

Authors:  J Nilsson; M Sjölund; L Palmberg; J Thyberg; C H Heldin
Journal:  Proc Natl Acad Sci U S A       Date:  1985-07       Impact factor: 11.205

3.  Evidence for a monoclonal origin of human atherosclerotic plaques and some implications.

Authors:  E P Benditt
Journal:  Circulation       Date:  1974-10       Impact factor: 29.690

Review 4.  Kinetics of atherosclerosis: a stem cell model.

Authors:  S M Schwartz; M R Reidy; A Clowes
Journal:  Ann N Y Acad Sci       Date:  1985       Impact factor: 5.691

5.  Examination of a spontaneously transformed aortic smooth muscle cell line. I. Morphological examinations.

Authors:  E Csonka; A S Koch; A Kádár; I Ováry
Journal:  Acta Morphol Hung       Date:  1984

6.  Rat vascular smooth muscle cells immortalized with SV40 large T antigen possess defined smooth muscle cell characteristics including growth inhibition by heparin.

Authors:  C F Reilly
Journal:  J Cell Physiol       Date:  1990-02       Impact factor: 6.384

7.  The presence of cytomegalovirus nucleic acids in arterial walls of atherosclerotic and nonatherosclerotic patients.

Authors:  M G Hendrix; P H Dormans; P Kitslaar; F Bosman; C A Bruggeman
Journal:  Am J Pathol       Date:  1989-05       Impact factor: 4.307

8.  Platelet-derived growth factor gene expression in human atherosclerotic plaques and normal artery wall.

Authors:  T B Barrett; E P Benditt
Journal:  Proc Natl Acad Sci U S A       Date:  1988-04       Impact factor: 11.205

9.  Growth-stimulating effect of catecholamines on rat aortic smooth muscle cells in culture.

Authors:  N Blaes; J P Boissel
Journal:  J Cell Physiol       Date:  1983-08       Impact factor: 6.384

10.  Focal smooth muscle proliferation in the aortic intima produced by an initiation-promotion sequence.

Authors:  M W Majesky; M A Reidy; E P Benditt; M R Juchau
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

View more
  9 in total

1.  Vessel size-dependent expression of intermediate-sized filaments, calponin, and h-caldesmon in smooth muscle cells of human coronary arteries.

Authors:  A Nakamura; S Isoyama; K Goto
Journal:  Heart Vessels       Date:  1999       Impact factor: 2.037

2.  Ring formation in cultures of rat aortic smooth muscle cells.

Authors:  E Bonanno; R F Nicosia
Journal:  In Vitro Cell Dev Biol       Date:  1992 Nov-Dec

3.  Changes in cultured arterial smooth muscle cells isolated from chicks upon cholesterol feeding.

Authors:  A Carazo; J Alejandre; R Diaz; A Ríos; M Castillo; A Linares
Journal:  Lipids       Date:  1998-02       Impact factor: 1.880

4.  Induction of microRNA-1 by myocardin in smooth muscle cells inhibits cell proliferation.

Authors:  Jie Chen; Hao Yin; Yulan Jiang; Sarvan Kumar Radhakrishnan; Zhan-Peng Huang; Jingjing Li; Zhan Shi; Elisabeth P C Kilsdonk; Yu Gui; Da-Zhi Wang; Xi-Long Zheng
Journal:  Arterioscler Thromb Vasc Biol       Date:  2010-11-04       Impact factor: 8.311

5.  The reversal of the inhibition on lipids synthesis by L-659,699 in arterial smooth muscle cells cultures.

Authors:  A Carazo; M J Alejandre; A Louktibi; A Linares
Journal:  Mol Cell Biochem       Date:  2001-05       Impact factor: 3.396

6.  Phenotype-specific inhibition of the vascular smooth muscle cell cycle by high glucose treatment.

Authors:  X-L Zheng; S-G Yuan; D-Q Peng
Journal:  Diabetologia       Date:  2007-02-14       Impact factor: 10.122

7.  Lipid biosynthesis in cultured arterial smooth muscle cells is related to their phenotype.

Authors:  E Dusserre; M C Bourdillon; M Ciavatti; C Covacho; S Renaud
Journal:  Lipids       Date:  1993-07       Impact factor: 1.880

8.  Identification, structural, and functional characterization of a new early gene (6A3-5, 7 kb): implication in the proliferation and differentiation of smooth muscle cells.

Authors:  Kazem Zibara; Gwenaële Garin; John L McGregor
Journal:  J Biomed Biotechnol       Date:  2005

9.  6A3-5/Osa2 is an early activated gene implicated in the control of vascular smooth muscle cell functions.

Authors:  Gwenaele Garin; Kazem Zibara; Frederick Aguilar; Ming Lo; Adam Hurlstone; Robin Poston; John L Mcgregor
Journal:  J Biomed Biotechnol       Date:  2006
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.