𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Induction of cell cycle-dependent genes during cell cycle progression of arterial smooth muscle cells in culture

✍ Scribed by Alain-Pierre Gadeau; Michel Campan; Claude Desgranges


Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
626 KB
Volume
146
Category
Article
ISSN
0021-9541

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Serum stimulation of arterial smooth muscle cells in culture induces a progression through the cell cycle and cell proliferation. Most genes previously described as cell cycle‐dependent in various cell types also demonstrate a cell cycle‐dependent expression in arterial smooth muscle cells. As in other cell types, these genes can be classified into three groups according to their mode of expression: “immediate early” genes (c‐fos, c‐myc,…), “delayed early” genes (2F1,…), and “late‐G1” genes (proliferating cell nuclear antigen, thymidine kinase,…). In addition to these previously described genes, three genes isolated from a cDNA library of stimulated smooth muscle cells have been demonstrated to be cell cycledependent: A21, the rat JE gene, and L51 can be classified as “immediate early” genes, while M11 represents a new member of the “delayed early” gene family.


📜 SIMILAR VOLUMES


Cell cycle dependent gene expression in
✍ Michel Campan; Claude Desgranges; Alain-Pierre Gadeau; Dominique Millet; Francis 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 892 KB

## Abstract The expression of a set of cell cycle dependent (CCD) genes (c‐fos, c‐myc, ornithine decarboxylase (ODC), and thymidine kinase (TK)) was comparatively studied in cultured arterial smooth muscle cells (SMC) during exit from quiescence and exponential proliferation. These genes, which wer

MEK hyperphosphorylation coincides with
✍ Sabina Vogel; Thomas Kubin; Dietmar von der Ahe; Elisabeth Deindl; Wolfgang Scha 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 89 KB

## Abstract Smooth muscle cells (SMCs) form the backbone of arteries and their proliferation hallmarks collateral vessel growth, a process termed arteriogenesis, as well as pathogenic responses such as restenosis. Since signaling pathways in SMCs are the main targets for therapeutic interventions,

MEK hyperphosphorylation coincides with
✍ Sabina Vogel; Thomas Kubin; Dietmar von der Ahe; Elisabeth Deindl; Wolfgang Scha 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 571 KB

## Abstract Smooth muscle cells (SMCs) form the backbone of arteries and their proliferation hallmarks collateral vessel growth, a process termed arteriogenesis, as well as pathogenic responses such as restenosis. Since signaling pathways in SMCs are the main targets for therapeutic interventions,

Changes in the cell cycle during culture
✍ Jennifer A. Marshall Graves; Kenneth W. Koschel 📂 Article 📅 1980 🏛 John Wiley and Sons 🌐 English ⚖ 617 KB

## Abstract Cell cycle studies, using PLM analysis, were carried out on a mouse‐Chinese hamster cell hybrid and its derivatives which stably retained all parental chromosomes during the year of study. Parameter estimates were obtained from the PLM curves, using conjugate gradient curve fitting proc

Alternative splicing and cycling kinetic
✍ Ingo Morano; Stefan Koehlen; Hannelore Haase; Gunter Erb; Leonidas G. Baltas; St 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 182 KB

We investigated in vivo expression of myosin heavy chain (MHC) isoforms, 17 kDa myosin light chain (MLC 17 ), and phosphorylation of the 20 kDa MLC (MLC 20 ) as well as mechanical performance of chemically skinned fibers of normal and hypertrophied smooth muscle (SM) of human myometrium. According t

SPARC regulates cell cycle progression i
✍ Aleksandar Francki; Kouros Motamed; Timothy D. McClure; Marcus Kaya; Carrie Murr 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 209 KB 👁 1 views

## Abstract Glomerular mesangial cells both synthesize and respond to insulin‐like growth factor‐1 (IGF‐1). Increased activity of the IGF signaling pathway has been implicated as a major contributor to renal enlargement and subsequent development of diabetic nephropathy. Secreted protein acidic and