Differentiation of Vascular Smooth Muscle Cells and the Regulation of Protein Kinase C-alpha
作者:
Hermann Haller,
Carsten Lindschau,
Petra Quass,
Armin Distler,
Friedrich C. Luft,
期刊:
Circulation Research
(OVID Available online 1995)
卷期:
Volume 76,
issue 1
页码: 21-29
ISSN:0009-7330
年代: 1995
出版商: OVID
数据来源: OVID
摘要:
Dedifferentiation and proliferation of vascular smooth muscle cells (VSMCs) are important features of atherosclerosis. The molecular mechanisms are largely unclear; however, protein kinase C (PKC) is a key enzyme in the intracellular signaling pathways that mediate this process. We studied the activity and immunoreactivity of PKC-alpha in primary cultures of VSMCs from rat aortas under different conditions of growth and differentiation. PKC-alpha was determined under the following conditions: (1) during the growth phase and after confluence of cultured (passages 1 through 3) VSMCs, (2) before and after induction of differentiation in VSMCs by retinoic acid, and (3) in primary cultures of VSMCs from spontaneously hypertensive rats (SHR) and Wistar-Kyoto (WKY) rats during early passages. PKC activity was measured by in vitro substrate phosphorylation. PKC-alpha immunoreactivity was assessed by Western blot using specific polyclonal antibodies and by immunostaining with confocal microscopy. Cell proliferation was measured by direct count. The cell phenotype was characterized by immunostaining and Western blot for alpha-actin and desmin. PKC-alpha expression and PKC activity during VSMC growth showed a decrease during rapid growth and an increase in confluent cells. This pattern was associated with the respective changes in cell differentiation. Retinoic acid induced an increase in PKC-alpha expression together with a more differentiated phenotype. Subcultured, rapidly growing VSMCs from SHR showed a decreased PKC-alpha expression compared with cells from WKY rats. To establish cause and effect, we next microinjected either PKC-alpha or inactivated material directly into dedifferentiated cells. We found that cells injected with active PKC-alpha expressed increased amounts of actin compared with control cells. We identified a close correlation between PKC-alpha and actin immunofluorescence. We conclude that PKC-alpha is downregulated in rapidly growing VSMCs. Our findings demonstrate an inverse association between PKC-alpha expression and VSMC differentiation. They suggest a role for downregulation of PKC-alpha in the proliferative response of these cells.(Circ Res. 1995;76:21-29.)
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