Retardation of phenotypic transition of rabbit arterial smooth muscle cells in three-dimensional primary culture

被引:14
作者
Yamamoto, M
Nakamura, H
Yamato, M
Aoyagi, M
Yamamoto, K
机构
[1] SAITAMA MED SCH,ELECTRON MICROSCOPY LAB,MOROYAMA,SAITAMA 35004,JAPAN
[2] NIHON UNIV,COLL PHARM,DEPT BIOCHEM,FUNABASHI,CHIBA 274,JAPAN
[3] TOKYO MED & DENT UNIV,DEPT NEUROSURG,BUNKYO KU,TOKYO 113,JAPAN
关键词
D O I
10.1006/excr.1996.0152
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Three-dimensional gel culture systems represent conditions that mimic the differentiated state of mesenchymal cells in vivo. We examined gel contraction, cell growth, and phenotypic modulation of rabbit arterial SMC in three-dimensional gel culture. The gel contraction rate was dependent on the collagen type; that is, the contraction by freshly isolated SMC was faster and more pronounced in type I collagen than in type III collagen. In contrast, the phenotypic modulation of SMC was independent of collagen type. The major portion of cells in both type I and III collagens with growth factors underwent transition from a contractile (G0 phase) to a synthetic phenotype (G1B phase), but this transition was clearly delayed compared with that on collagens. The cells had hardly begun DNA synthesis in either collagen type and failed to proliferate even after 10 days of culture. These results indicate that collagen type is important in gel contraction by vascular SMC, while the organization of collagen fibrils (two-dimensional vs three-dimensional) is more critical in the phenotypic transition and proliferation of these cells. However, the more specific organization of extracellular matrix than the collagen gel culture system may be necessary to maintain the contractile phenotype of SMC. (C) 1996 Academic Press, Inc.
引用
收藏
页码:12 / 21
页数:10
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