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细胞培养中的肢体芽软骨形成,特别涉及培养基中的血清浓度。

Limb bud chondrogenesis in cell culture, with particular reference to serum concentration in the culture medium.

作者信息

Hattori T, Ide H

出版信息

Exp Cell Res. 1984 Feb;150(2):338-46. doi: 10.1016/0014-4827(84)90577-9.

Abstract

When limb bud mesodermal cells of stages 23-24 chick embryos were plated at low cell density (2 X 10(5) cells/cm2) and cultured in medium containing 10% fetal calf serum (FCS) (serum-rich medium), all cells became fibroblastic and no chondrocyte differentiation occurred in the culture. However, when cells of the same origin were cultured in a medium containing only 0.1% FCS (serum-poor medium), almost all the cells formed aggregates which developed further to form cartilage nodules. The loss of chondrogenic activity in serum-rich medium culture was irreversible: cultivation of the limb bud cells in serum-rich medium for 12 h abolished chondrogenic activity completely and these cells could not resume activity on re-cultivation in serum-poor medium. Calf, horse and chick serum at a concentration of 10% also induced the loss of chondrogenic activity in low cell density culture. Failure of chondrogenesis in serum-rich medium culture seemed to be due to the commitment of bipotential limb bud mesodermal cells to fibroblastic cells rather than to selective detachment of pre-committed chondroblasts.

摘要

将23-24期鸡胚的肢芽中胚层细胞以低细胞密度(2×10⁵个细胞/cm²)接种,并在含有10%胎牛血清(FCS)的培养基(富血清培养基)中培养时,所有细胞都变成了成纤维细胞,培养物中未发生软骨细胞分化。然而,当相同来源的细胞在仅含有0.1%FCS的培养基(贫血清培养基)中培养时,几乎所有细胞都形成了聚集体,并进一步发育形成软骨结节。富血清培养基培养中软骨生成活性的丧失是不可逆的:肢芽细胞在富血清培养基中培养12小时会完全消除软骨生成活性,这些细胞在重新接种到贫血清培养基中时无法恢复活性。浓度为10%的小牛、马和鸡血清在低细胞密度培养中也会导致软骨生成活性丧失。富血清培养基培养中软骨形成失败似乎是由于双能性肢芽中胚层细胞定向分化为成纤维细胞,而不是预先定向的软骨细胞选择性脱离所致。

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