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一种用于支持细胞的新型灌流双室培养系统的特性:细胞外基质对转铁蛋白分泌的细胞通透性和动力学的影响

Characterization of a new superfusion, two-compartment culture system for Sertoli cells: influence of extracellular matrix on the cell permeability and dynamics of transferrin secretion.

作者信息

Guillou F

机构信息

Unité Endocrinologie de la gamétogenèse, INRA, CNRS URA 1291, Nouzilly, France.

出版信息

J Androl. 1990 Mar-Apr;11(2):182-94.

PMID:2324005
Abstract

A new superfusion two-compartment culture system was developed in the laboratory of the author and was used to investigate the influence of testicular extracellular matrix on barrier formation by Sertoli cells in culture, and the acute dynamic changes in the bidirectional secretion of transferrin. Only Sertoli cells growing on extracellular matrix formed a monolayer that was specifically impermeable to inulin, peroxidase, and FSH, but did not affect the passage of testosterone. Moreover, in these conditions, they were highly polarized morphologically. The bidirectional secretion (basal/apical ratio) of transferrin was affected by the duration of the stationary culture preceding the superfusion. After 2 days of culture, the amount of transferrin secreted during the subsequent 20 h superfusion was higher in the basal chamber than in the apical chamber. In contrast, after 5 days of culture, the amount of secreted transferrin was higher in the apical compartment. The author compared his data with those previously reported by other authors, using stationary two-compartment chambers.

摘要

作者所在实验室开发了一种新型的双室灌注培养系统,用于研究睾丸细胞外基质对培养的支持细胞屏障形成的影响,以及转铁蛋白双向分泌的急性动态变化。只有生长在细胞外基质上的支持细胞形成了单层,该单层对菊粉、过氧化物酶和促卵泡激素具有特异性的不透性,但不影响睾酮的通过。此外,在这些条件下,它们在形态上高度极化。转铁蛋白的双向分泌(基底/顶端比率)受灌注前静止培养持续时间的影响。培养2天后,在随后20小时的灌注过程中,基底室分泌的转铁蛋白量高于顶端室。相反,培养5天后,顶端室分泌的转铁蛋白量更高。作者将自己的数据与其他作者先前使用静止双室培养箱报告的数据进行了比较。

相似文献

1
Characterization of a new superfusion, two-compartment culture system for Sertoli cells: influence of extracellular matrix on the cell permeability and dynamics of transferrin secretion.一种用于支持细胞的新型灌流双室培养系统的特性:细胞外基质对转铁蛋白分泌的细胞通透性和动力学的影响
J Androl. 1990 Mar-Apr;11(2):182-94.
2
Polarized secretion of androgen-binding protein and transferrin by Sertoli cells grown in a bicameral culture system.在双室培养系统中生长的支持细胞对雄激素结合蛋白和转铁蛋白的极化分泌。
Endocrinology. 1987 Mar;120(3):1097-103. doi: 10.1210/endo-120-3-1097.
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Characterization of Sertoli cells cultured in the bicameral chamber system: relationship between formation of permeability barriers and polarized secretion of transferrin.双室系统中培养的支持细胞的特性:通透性屏障形成与转铁蛋白极化分泌之间的关系。
Biol Reprod. 1990 Oct;43(4):672-83. doi: 10.1095/biolreprod43.4.672.
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Modulation of Sertoli cell functions in the two-chamber assembly by peritubular cells and extracellular matrix.在双室组件中,睾丸支持细胞功能受睾丸间质细胞和细胞外基质的调节。
Endocrinology. 1988 Jun;122(6):2604-12. doi: 10.1210/endo-122-6-2604.
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Direct toxic effects of clinical doses of chloroquine on transferrin secretion in immature rat sertoli cells in vitro.氯喹临床剂量对体外培养的未成熟大鼠支持细胞转铁蛋白分泌的直接毒性作用。
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Vectorial secretion of inhibin by immature rat Sertoli cells in vitro: reexamination of previous results.未成熟大鼠支持细胞体外抑制素的向量分泌:对先前结果的重新审视
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Bipolar secretion of androgen-binding protein and transferrin by Sertoli cells cultured in a two-compartment culture chamber.在两室培养室中培养的支持细胞对雄激素结合蛋白和转铁蛋白的双相分泌。
Endocrinology. 1987 Jan;120(1):291-8. doi: 10.1210/endo-120-1-291.
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Control of levels of plasminogen activator activity secreted by Sertoli cells maintained in a two-chamber assembly.
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Study of the dynamics of Sertoli cell secretions in a new superfusion, two-compartment culture system.新型双室灌流培养系统中支持细胞分泌动力学的研究
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Secreted products and extracellular matrix from testicular peritubular myoid cells influence androgen-binding protein secretion by Sertoli cells in culture.睾丸生精小管肌样细胞分泌的产物和细胞外基质影响培养的支持细胞雄激素结合蛋白的分泌。
J Androl. 1995 Jan-Feb;16(1):28-35.

引用本文的文献

1
Immortalized germ cells undergo meiosis in vitro.永生化生殖细胞在体外进行减数分裂。
Proc Natl Acad Sci U S A. 1994 Jun 7;91(12):5533-7. doi: 10.1073/pnas.91.12.5533.
2
Expression of fetal-type intermediate filaments by 17-day-old rat Sertoli cells cultured on reconstituted basement membrane.在重组基底膜上培养的17日龄大鼠支持细胞中胎儿型中间丝的表达。
Cell Tissue Res. 1990 May;260(2):395-401. doi: 10.1007/BF00318642.