Literature DB >> 10640447

Induction of high mobility group I architectural transcription factors in proliferating vascular smooth muscle in vivo and in vitro.

M T Chin1, A Pellacani, C M Hsieh, S S Lin, M K Jain, A Patel, G S Huggins, R Reeves, M A Perrella, M E Lee.   

Abstract

Proliferation of vascular smooth muscle cells (VSMCs) is a hallmark of arteriosclerosis. Architectural transcription factors of the high mobility group (HMG)-I family have been implicated in the control of cell proliferation and gene expression. We studied the pattern of HMG-I mRNA and protein expression in proliferating VSMCs. HMG-I(Y) and HMGI-C mRNAs were barely detectable by Northern analysis in samples prepared from uninjured rat carotid arteries. In contrast, these mRNAs were induced dramatically in carotid arteries 2 and 5-6 days after balloon injury. By in situ hybridization at 6 days after injury, the induced mRNAs localized to smooth muscle cells of the developing neointima, and immunocytochemical analysis showed that HMG-I(Y) protein was expressed in the nuclei of these cells. To confirm this association between HMG-I protein induction and cell growth, we assessed HMG-I(Y) and HMGI-C mRNA expression in rat aortic smooth muscle cells (RASMCs) in primary culture. The HMG-I mRNAs were barely detectable in quiescent RASMCs but were induced markedly by serum stimulation. This induction of mRNA by serum was time dependent and peaked at 9 h. Western blot analysis confirmed that HMG-I(Y) protein induction also occurred in vitro. To our knowledge, this is the first demonstration of induction of HMG-I protein expression in proliferating RASMCs in vivo and in vitro. This demonstration suggests that the HMG-I proteins may play an important role in smooth muscle cell proliferation. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10640447     DOI: 10.1006/jmcc.1999.1054

Source DB:  PubMed          Journal:  J Mol Cell Cardiol        ISSN: 0022-2828            Impact factor:   5.000


  5 in total

Review 1.  The HMG I proteins: dynamic roles in gene activation, development, and tumorigenesis.

Authors:  F Liu; K Y Chau; P Arlotta; S J Ono
Journal:  Immunol Res       Date:  2001       Impact factor: 2.829

Review 2.  Regulation of smooth muscle phenotype.

Authors:  Ichiro Manabe; Ryozo Nagai
Journal:  Curr Atheroscler Rep       Date:  2003-05       Impact factor: 5.113

3.  Repression of smooth muscle differentiation by a novel high mobility group box-containing protein, HMG2L1.

Authors:  Jiliang Zhou; Guoqing Hu; Xiaobo Wang
Journal:  J Biol Chem       Date:  2010-05-27       Impact factor: 5.157

4.  High mobility group A2 protein and its derivatives bind a specific region of the promoter of DNA repair gene ERCC1 and modulate its activity.

Authors:  Lars Borrmann; Ralf Schwanbeck; Tomasz Heyduk; Birte Seebeck; Piere Rogalla; Jörn Bullerdiek; Jacek R Wisniewski
Journal:  Nucleic Acids Res       Date:  2003-12-01       Impact factor: 16.971

5.  Mesenchymal stromal cells expressing a dominant-negative high mobility group A1 transgene exhibit improved function during sepsis.

Authors:  Min-Young Kwon; Sailaja Ghanta; Julie Ng; Ana P Castano; Junwen Han; Bonna Ith; James A Lederer; Souheil El-Chemaly; Su Wol Chung; Xiaoli Liu; Mark A Perrella
Journal:  J Leukoc Biol       Date:  2021-01-13       Impact factor: 4.962

  5 in total

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