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体外培养的内淋巴囊细胞的透明质酸合成

Hyaluronan synthesis by in vitro cultured endolymphatic sac cells.

作者信息

Amoils C P, Schindler R A, Parker D A, Hradek G T

机构信息

Department of Otolaryngology, Coleman and Epstein Neurotological Laboratories, University of California, San Francisco 94117.

出版信息

Am J Otol. 1992 Jul;13(4):303-7.

PMID:1415490
Abstract

The endolymphatic sac (ELS) has been the subject of investigation for many years and yet its overall function remains unclear. It is believed mainly to be involved in the regulation of endolymph through fluid resorption and secretion of osmotically active substances. The present study was performed using in vitro cultured, fetal ELSs of 18 to 19 day gestational mice, to assess whether the ELS cells can synthesize the osmotically active polysaccharide, hyaluronan (HA). The ELS and portions of the membranous labyrinth were dissected from whole otocyst specimens and placed in 14C glucose-enhanced tissue culture media. A light microscopic (LM), autoradiographic study was performed to assess whether 14C glucose could be incorporated by the tissue into HA. Both the ELS cells and the adjacent cartilage demonstrated radiolabel incorporation within 4 hours of incubation in tissue culture medium, with increased radiolabel density in ELS cells after 24 hours of incubation. HA-specific hyaluronidase (HAase) resulted in removal of HAase-sensitive compounds in the ELS in both 4-hour and 24-hour cultured specimens when compared to adjacent cartilage cells (p = 0.001). Approximately 43 percent of the radiolabel was incorporated into HA in ELS specimens, as compared to a 22 percent HA synthesis in the adjacent cartilage tissue, suggesting preferential synthesis by ELS cells. The dissected murine otocysts demonstrate viability in vitro as measured by their ability to incorporate 14C glucose from tissue culture medium. Under these conditions the cultured ELS demonstrates an ability to synthesize HA. A theory of ELS function is proposed.

摘要

内淋巴囊(ELS)多年来一直是研究的对象,但其整体功能仍不清楚。人们认为它主要通过液体重吸收和渗透活性物质的分泌参与内淋巴的调节。本研究使用妊娠18至19天小鼠的体外培养胎儿ELS进行,以评估ELS细胞是否能合成渗透活性多糖透明质酸(HA)。从整个耳囊标本中解剖出ELS和部分膜迷路,并置于含14C葡萄糖的组织培养基中。进行了光镜(LM)放射自显影研究,以评估组织能否将14C葡萄糖掺入HA中。在组织培养基中孵育4小时内,ELS细胞和相邻软骨均显示有放射性标记掺入,孵育24小时后ELS细胞中的放射性标记密度增加。与相邻软骨细胞相比,HA特异性透明质酸酶(HAase)在4小时和24小时培养的标本中均导致ELS中对HAase敏感的化合物被去除(p = 0.001)。ELS标本中约43%的放射性标记掺入了HA,而相邻软骨组织中的HA合成率为22%,这表明ELS细胞优先合成HA。解剖的小鼠耳囊在体外通过其从组织培养基中摄取14C葡萄糖的能力来证明其活力。在这些条件下,培养的ELS显示出合成HA的能力。提出了一种ELS功能理论。

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