肾切除动物模型代偿性肾肥大和增生机制的研究。利用组织培养在未切除肾的兔血清中发现嗜肾性生长刺激因子的证据。

Investigative urology Pub Date : 1981-03-01
H Kanetake, N Yamamoto
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引用次数: 0

摘要

当同步原代兔肾融合单层细胞培养物与含有未切除肾的兔血清的培养基孵育时,氚化胸腺嘧啶与DNA的结合比含有正常兔血清的培养基大得多。未去肾血清对胸腺嘧啶掺入稀疏培养细胞的最大促生长活性比正常血清提高了约5倍。我们得出结论,未切除的血清含有一种生长刺激因子。未去肾兔血清对兔皮肤原代培养细胞DNA合成的刺激作用不高于正常兔血清,说明未去肾兔血清中的生长刺激因子在组织培养中具有嗜肾性特异性。转化的兔肾细胞系RK-13对嗜肾性生长刺激因子无反应。然而,原代和转化的兔肾细胞从未切除的血清中吸收嗜肾性生长刺激因子。因此,细胞系RK-13具有吸附嗜肾性生长因子的受体,但不能进一步响应生长刺激过程。嗜肾性生长刺激因子是热不稳定的,不能被孔径高达12000分子量的透析管透析。因此,嗜肾性生长因子似乎是一种大分子,可能是一种蛋白质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Studies on the mechanism of compensatory renal hypertrophy and hyperplasia in a nephrectomized animal model. I. Evidence for a renotropic growth stimulating factor in uninephrectomized rabbit sera using tissue culture.

When synchronized primary rabbit kidney confluent monolayer cell cultures were incubated with a medium that contained uninephrectomized rabbit serum, the incorporation of tritiated thymidine into DNA was much greater than that with a medium that contained normal rabbit serum. The maximal growth stimulating activity of uninephrectomized serum on thymidine incorporation into sparsely cultured cells was increased approximately 5 fold above that of normal serum. We conclude that uninephrectomized sera contain a growth stimulating factor. Uninephrectomized rabbit sera showed no increased stimulation of DNA synthesis in primary rabbit skin cultured cells above that by normal rabbit serum, indicating that the growth stimulating factor in uninephrectomized serum shows renotropic specificity in tissue culture. A transformed rabbit kidney cell line RK-13 did not respond to the renotropic growth stimulating factor. However, primary and the transformed rabbit kidney cells absorbed the renotropic growth stimulating factor from uninephrectomized sera. Thus, the cell line RK-13 has receptors for adsorption of the renotropic growth factor but is unable to respond further to the growth stimulating process. The renotropic growth stimulating factor is heat unstable and undialyzable by dialysis tubings with pore size up to 12,000 molecular weight. Thus the renotropic growth factor seems to be a macromolecule, probably a protein.

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