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地塞米松对含血清颅盖骨细胞培养物中软骨表达和维持的影响。

Effects of dexamethasone on expression and maintenance of cartilage in serum-containing cultures of calvaria cells.

作者信息

Bellows C G, Heersche J N, Aubin J E

机构信息

Medical Research Council Group in Periodontal Physiology, Faculty of Dentistry, University of Toronto, Ontario, Canada.

出版信息

Cell Tissue Res. 1989 Apr;256(1):145-51. doi: 10.1007/BF00224728.

DOI:10.1007/BF00224728
PMID:2713890
Abstract

The effects of dexamethasone on the ability of cells enzymatically isolated from 21-day fetal rat calvaria to produce cartilage in vitro has been investigated. Primary cultures of single-cell suspensions of rat calvaria were grown for up to 28 days in vitro in alpha-minimal essential medium containing 15% fetal bovine serum, 50 micrograms/ml ascorbic acid, 10 mM Na beta-glycerophosphate and dexamethasone at concentrations of 1 microM to 1 nM. Two types of nodules were present in dexamethasone-containing cultures. One has been characterized previously as bone (Bellows et al. 1986). The second morphologically resembled hyaline cartilage, possessed a strong Alcian blue-positive matrix and contained type-II, but not type-I, collagen. Both bone and cartilaginous nodules were spatially distinct and developed in isolation from each other. Cartilaginous nodules were found in the highest number at a dexamethasone concentration of 100 nM. Time-course experiments revealed that while the number of bone nodules increased continuously at least to day 28, the number of cartilaginous nodules remained constant after cultures had reached confluency. When cells were isolated separately from frontal and parietal bones and sutural regions, the greatest number of cartilaginous nodules developed from parietal bones. Since 21-day fetal rat calvaria contains 2 distinct patches of cartilage at the periphery of the parietal bones, it seems likely that this cartilaginous tissue is the origin of the cartilage cells. The results demonstrate that cultures of rat calvaria cells contain chondrocytes and possibly chondroprogenitor cells that are distinct from osteoprogenitors.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

已研究地塞米松对从21日龄胎鼠颅骨酶解分离的细胞在体外产生软骨能力的影响。将大鼠颅骨单细胞悬液的原代培养物在含有15%胎牛血清、50微克/毫升抗坏血酸、10毫摩尔/升β-甘油磷酸钠以及浓度为1微摩尔至1纳摩尔的地塞米松的α-最低必需培养基中体外培养长达28天。在含地塞米松的培养物中存在两种类型的结节。一种先前已被鉴定为骨(贝洛斯等人,1986年)。另一种在形态上类似于透明软骨,具有强烈的阿利新蓝阳性基质,并且含有II型而非I型胶原蛋白。骨结节和软骨结节在空间上是分开的,并且彼此独立发育。在地塞米松浓度为100纳摩尔时发现软骨结节数量最多。时间进程实验表明,虽然骨结节数量至少持续增加至第28天,但软骨结节数量在培养物达到汇合后保持恒定。当分别从额骨、顶骨和缝合区域分离细胞时,从顶骨发育出的软骨结节数量最多。由于21日龄胎鼠颅骨在顶骨周边含有两块不同的软骨,这种软骨组织似乎很可能是软骨细胞的来源。结果表明,大鼠颅骨细胞培养物含有与骨祖细胞不同的软骨细胞以及可能的软骨祖细胞。(摘要截短至250字)

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