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小鼠肾细胞无血清原代培养物中糖鞘脂的表达:雌雄差异及雄激素敏感性

Expression of glycosphingolipids in serum-free primary cultures of mouse kidney cells: male-female differences and androgen sensitivity.

作者信息

Gross S K, Lyerla T A, Evans J E, McCluer R H

机构信息

E.K. Shriver Center for Mental Retardation, Waltham, MA 02254.

出版信息

Mol Cell Biochem. 1994 Aug 17;137(1):25-31. doi: 10.1007/BF00926036.

Abstract

The expression of neutral glycosphingolipids was examined in primary kidney cell cultures derived from adult male and female beige mutant mice (C57BL/6J;bgj/bgj) with enrichment for proximal tubule cells during preparation of explants and using defined serum-free medium for the culture conditions. Cells proliferated for 7 days in vitro to provide confluent or nearly confluent monolayers of epithelial-type growth indicative of proximal tubule cells. The male vs female differences in neutral glycosphingolipids seen in the kidney in vivo were retained in these 7 day cultures. Cultures derived from males contained galacto- and digalactosylceramides whereas those from females did not express these types of glycolipids. Also, male cells had higher ratios of sphingosine: phytosphingosine containing species in Nfa (non-hydroxy fatty acid) globotriaosylceramide and in glucosylceramide than females. The shift in sphingosine: phytosphingosine to male ratios in Nfa globotriaosylceramide and in glucosylceramide could be stimulated in female kidney cells by treatment with 10(-5) M testosterone or 5 alpha-dihydrotestosterone. The male-specific expression of neutral glycosphingolipids, then, appears to be stable character of male-type differentiation in mouse kidney that is passed on during proliferation in culture. Female kidney cells retain an ability to respond to androgens with specific changes in neutral glycosphingolipid expression during 7 days of growth in vitro in serum-free conditions, but do not respond with the induction of the male-specific glycolipids galacto- and digalactosylceramides as seen in vivo.

摘要

在成年雄性和雌性米色突变小鼠(C57BL/6J;bgj/bgj)的原代肾细胞培养物中检测了中性糖鞘脂的表达。在制备外植体时富集近端小管细胞,并使用限定的无血清培养基进行培养条件。细胞在体外增殖7天,形成汇合或接近汇合的上皮型生长单层,表明为近端小管细胞。体内肾脏中观察到的中性糖鞘脂的雄性与雌性差异在这些7天的培养物中得以保留。来自雄性的培养物含有半乳糖神经酰胺和二半乳糖神经酰胺,而来自雌性的培养物不表达这些类型的糖脂。此外,在Nfa(非羟基脂肪酸)球三糖神经酰胺和葡萄糖神经酰胺中,雄性细胞中鞘氨醇:植物鞘氨醇含有的物种的比例高于雌性。用10^(-5) M睾酮或5α-二氢睾酮处理雌性肾细胞,可刺激Nfa球三糖神经酰胺和葡萄糖神经酰胺中鞘氨醇:植物鞘氨醇向雄性比例的转变。因此,中性糖鞘脂的雄性特异性表达似乎是小鼠肾脏中雄性型分化的稳定特征,在培养增殖过程中得以传递。在无血清条件下体外生长7天期间,雌性肾细胞保留了对雄激素作出反应并使中性糖鞘脂表达发生特定变化的能力,但不会像在体内那样通过诱导雄性特异性糖脂半乳糖神经酰胺和二半乳糖神经酰胺作出反应。

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