𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Cell cycle dependent gene expression in quiescent stimulated and asynchronously cycling arterial smooth muscle cells in culture

✍ Scribed by Michel Campan; Claude Desgranges; Alain-Pierre Gadeau; Dominique Millet; Francis Belloc


Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
892 KB
Volume
150
Category
Article
ISSN
0021-9541

No coin nor oath required. For personal study only.

✦ Synopsis


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 were not expressed in quiescent SMC, were chronologically induced after serum stimulation. c‐fos mRNA were rapidly and transiently expressed very early in the G~1~ phase; c‐myc and ODC peaked a few hours after serum stimulation and then remained at an intermediary level throughout the first cell cycle; TK mRNA and activity then appeared at the G~1~/S boundary and peak in G~2~/M phases. Except for c‐fos, the other genes were also expressed in asynchronously cycling SMC (ACSMC); their expression was studied in elutriated subpopulations representative of cell cycle progression. c‐fos mRNA were undetectable in any sorted subpopulations, even in the pure early G~1~ population. Despite a slight increase as the cell cycle advanced, c‐myc and ODC genes were expressed throughout the ACSMC cell cycle. A faint TK activity was found in G~1~ subpopulations and increased in populations enriched in other phases; in contrast, TK mRNA remained highly expressed in all elutriated subpopulations. This study demonstrates significant modulations in CCD gene expression between quiescent stimulated and asynchronously cycling SMC in culture. This suggests that the events occurring during the emergence of SMC from quiescence are probably different from those in the G~1~ phase of ACSMC.


📜 SIMILAR VOLUMES


Induction of cell cycle-dependent genes
✍ Alain-Pierre Gadeau; Michel Campan; Claude Desgranges 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 626 KB

## 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 ce

Regulation of expression of the growth-s
✍ Mark S. Kindy; Karen E. Brown; Gail E. Sonenshein 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 611 KB

Vascular smooth muscle cells (SMCs) play a key role in the development of major arteries. Furthermore, abnormal growth of vascular smooth muscle cells has been implicated in the progression of major diseases of the cardiovascular system. Here, we report detection in primary cultures of bovine vascul

Cell cycle behavior and MyoD expression
✍ Moor, A.N.; Rector, E.S.; Anderson, J.E. 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 219 KB 👁 1 views

Since mdx limb muscle regeneration in vivo is accompanied by rapid myoblast proliferation and differentiation compared to normal, we tested the possibility that proliferation and differentiation were differentially regulated in normal and mdx dystrophic muscle cells. Cell cycle behavior, MyoD expres

Regional, developmental, and cell cycle-
✍ Anne Stiene-Martin; Rong Zhou; Kurt F. Hauser 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 596 KB

The diversity of opioid receptor expression was examined in astrocytes in low-density and non-dividing (confluent) cultures from the cerebral cortex, hippocampus, cerebellum, and striatum of 1-day-old mice. µ, ␦, and opioid receptor expression was assessed in individual cells immunocytochemically, b

Differential expression of the keratinoc
✍ Jeffrey A. Winkles; Gregory F. Alberts; Marcio Chedid; William G. Taylor; Sabina 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 148 KB 👁 2 views

Keratinocyte growth factor (KGF) is a secreted member of the fibroblast growth factor (FGF) family of heparin-binding proteins. Studies reported to date indicate that it functions primarily as an important paracrine mediator of epithelial cell growth and differentiation. KGF appears to act via bindi

Plasminogen activator inhibitor type-1 g
✍ Rohan Samarakoon; Craig E. Higgins; Stephen P. Higgins; Stacie M. Kutz; Paul J. 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 536 KB

## Abstract Transforming growth factor‐β1 (TGF‐β1) stimulates expression of plasminogen activator inhibitor type‐1 (PAI‐1), a serine protease inhibitor (__SERPIN__) important in the control of stromal barrier proteolysis and cell‐to‐matrix adhesion. Pharmacologic agents that target MEK (PD98059, U0