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软骨细胞PRG4表型的微环境调节

Microenvironment regulation of PRG4 phenotype of chondrocytes.

作者信息

Blewis Megan E, Schumacher Barbara L, Klein Travis J, Schmidt Tannin A, Voegtline Michael S, Sah Robert L

机构信息

Department of Bioengineering, University of California-San Diego, La Jolla, California 92093-0412, USA.

出版信息

J Orthop Res. 2007 May;25(5):685-95. doi: 10.1002/jor.20307.

Abstract

Articular cartilage is a heterogeneous tissue with superficial (S), middle (M), and deep (D) zones. Chondrocytes in the S zone secrete the lubricating PRG4 protein, while chondrocytes from the M and D zones are more specialized in producing large amounts of the glycosaminoglycan (GAG) component of the extracellular matrix. Soluble and insoluble chemicals and mechanical stimuli regulate cartilage development, growth, and homeostasis; however, the mechanisms of regulation responsible for the distinct PRG4-positive and negative phenotypes of chondrocytes are unknown. The objective of this study was to determine if interaction between S and M chondrocytes regulates chondrocyte phenotype, as determined by coculture in monolayer at different ratios of S:M (100:0, 75:25, 50:50, 25:75, 0:100) and at different densities (240,000, 120,000, 60,000, and 30,000 cells/cm(2)), and by measurement of PRG4 secretion and expression, and GAG accumulation. Coculture of S and M cells resulted in significant up-regulation in PRG4 secretion and the percentage of cells expressing PRG4, with simultaneous down-regulation of GAG accumulation. Tracking M cells with PKH67 dye in coculture revealed that they maintained a PRG4-negative phenotype, and proliferated less than S cells. Taken together, these results indicate that the up-regulated PRG4 expression in coculture is a result of preferential proliferation of PRG4-expressing S cells. This finding may have practical implications for generating a large number of phenotypically normal S cells, which can be limited in source, for tissue engineering applications.

摘要

关节软骨是一种具有表层(S)、中层(M)和深层(D)区域的异质组织。S区的软骨细胞分泌润滑蛋白PRG4,而M区和D区的软骨细胞则更专门地产生细胞外基质的大量糖胺聚糖(GAG)成分。可溶性和不溶性化学物质以及机械刺激调节软骨的发育、生长和稳态;然而,负责软骨细胞不同PRG4阳性和阴性表型的调节机制尚不清楚。本研究的目的是确定S和M软骨细胞之间的相互作用是否调节软骨细胞表型,通过以不同的S:M比例(100:0、75:25、50:50、25:75、0:100)和不同密度(240,000、120,000、60,000和30,000个细胞/cm²)在单层中共培养,并测量PRG4分泌和表达以及GAG积累来确定。S和M细胞的共培养导致PRG4分泌和表达PRG4的细胞百分比显著上调,同时GAG积累下调。在共培养中用PKH67染料追踪M细胞发现,它们保持PRG4阴性表型,并且增殖比S细胞少。综上所述,这些结果表明共培养中PRG4表达上调是表达PRG4的S细胞优先增殖的结果。这一发现可能对为组织工程应用生成大量表型正常但来源可能有限的S细胞具有实际意义。

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