特定前列腺素可增强扩增后的成人关节软骨细胞的软骨形成。

Chondrogenesis of expanded adult human articular chondrocytes is enhanced by specific prostaglandins.

作者信息

Jakob M, Démarteau O, Suetterlin R, Heberer M, Martin I

机构信息

Institute for Surgical Research and Hospital Management, University Hospital Basel, Hebelstrasse 20, ZLF, Room 405, 4031 Basel, Switzerland.

出版信息

Rheumatology (Oxford). 2004 Jul;43(7):852-7. doi: 10.1093/rheumatology/keh197. Epub 2004 Apr 27.

Abstract

OBJECTIVE

To investigate the effects of the cyclooxygenase-2 (cox-2)-dependent prostaglandins D(2) (PGD(2)), E(2) (PGE(2)) and F(2)alpha (PGF(2)alpha) on the redifferentiation and cartilage matrix production of dedifferentiated articular chondrocytes.

METHODS

Human articular chondrocytes from three adult donors were dedifferentiated by monolayer expansion and induced to redifferentiate by culture as 3D pellets in a defined serum-free medium containing TGF-beta(1) and dexamethasone, without or with further supplementation with PGD(2), PGE(2) or PGF(2)alpha. After 2 weeks, pellets were assessed histologically, immunohistochemically, biochemically and by real-time quantitative reverse transcriptase-polymerase chain reaction.

RESULTS

All three PGs, but predominantly PGE(2), reduced the staining intensity of pellets for collagen type I, whereas PGD(2) and PGF(2)alpha increased the staining intensity of pellets for collagen type II and glycosaminoglycans (GAG). The GAG/DNA content of pellets was not affected by PGE(2) but was increased 1.5- and 2.1-fold by PGD(2) and PGF(2)alpha respectively. PGE(2) reduced the expression of collagen type I mRNA (9.0-fold), whereas PGD(2) and PGF(2)alpha increased the mRNA expression of collagen type II (6.2- and 4.1-fold respectively) and aggrecan (29.8- and 10.7-fold respectively).

CONCLUSION

In contrast to PGE(2), PGD(2) and PGF(2)alpha enhanced chondrogenic differentiation and hyaline cartilage matrix deposition by expanded human articular chondrocytes, and could thus be used to improve in vitro or in vivo cartilage regeneration approaches based on these cells.

摘要

目的

研究环氧化酶-2(COX-2)依赖性前列腺素D2(PGD2)、E2(PGE2)和F2α(PGF2α)对去分化关节软骨细胞再分化及软骨基质产生的影响。

方法

从三名成年供体获取人关节软骨细胞,通过单层扩增使其去分化,并在含有转化生长因子-β1(TGF-β1)和地塞米松的特定无血清培养基中作为三维微球培养以诱导其再分化,培养基中不添加或进一步添加PGD2、PGE2或PGF2α。2周后,对微球进行组织学、免疫组织化学、生物化学评估以及实时定量逆转录聚合酶链反应检测。

结果

所有三种前列腺素均可降低Ⅰ型胶原微球的染色强度,但主要是PGE2;而PGD2和PGF2α可增加Ⅱ型胶原和糖胺聚糖(GAG)微球的染色强度。微球的GAG/DNA含量不受PGE2影响,但分别被PGD2和PGF2α增加了1.5倍和2.1倍。PGE2降低了Ⅰ型胶原mRNA的表达(9.0倍),而PGD2和PGF2α增加了Ⅱ型胶原(分别为6.2倍和4.1倍)和聚集蛋白聚糖(分别为29.8倍和10.7倍)的mRNA表达。

结论

与PGE2相反,PGD2和PGF2α可增强人关节软骨细胞去分化后的软骨形成分化及透明软骨基质沉积,因此可用于改善基于这些细胞的体外或体内软骨再生方法。

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