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生长因子对大鼠甲状腺滤泡细胞增殖的调控

Growth factor control of rat thyroid follicular cell proliferation.

作者信息

Smith P, Wynford-Thomas D, Stringer B M, Williams E D

出版信息

Endocrinology. 1986 Oct;119(4):1439-45. doi: 10.1210/endo-119-4-1439.

Abstract

We have investigated the proliferative responses of rat thyroid follicular cells in serum-free culture to a range of growth factors including TSH, epidermal growth factor, and insulin, added singly or in combination. Follicles released from normal thyroids by collagenase/dispase digestion were cultured in suspension in agarose-coated microtiter plates to prevent monolayer formation. Growth responses were measured by [3H] thymidine incorporation and by autoradiography over successive 24- or 36-h periods. Insulin, even in the absence of other growth factors, stimulated [3H]thymidine incorporation in a concentration-dependent manner, rising from basal levels of 486 +/- (SE) 18 cpm to 4222 +/- 367 cpm/5 X 10(4) cells at 8 micrograms/ml. In contrast, TSH alone had no effect. In the presence of threshold levels (0.08 micrograms/ml) of insulin, however, there was a highly significant (P less than 0.001) response to TSH, [3H]thymidine incorporation rising from 1089 +/- 163 cpm in the absence of TSH to a maximum of 7548 +/- 585 with 1 mU/ml TSH. There was a synergistic interaction between insulin and TSH over the concentrations tested. Epidermal growth factor either alone or in combination with insulin failed to produce a significant response. Parallel autoradiographic studies were concordant with the [3H]thymidine incorporation data. We conclude that whereas in the absence of other growth factors TSH is unable to stimulate DNA synthesis in isolated rat thyroid follicles, the inclusion of just a single growth factor, insulin, permits a marked response. These observations emphasize the need for inclusion of appropriate permissive growth factor(s) when assessing the in vitro effect of a suspected tissue-specific mitogen.

摘要

我们研究了无血清培养条件下大鼠甲状腺滤泡细胞对一系列生长因子(包括促甲状腺激素、表皮生长因子和胰岛素,单独添加或联合添加)的增殖反应。通过胶原酶/分散酶消化从正常甲状腺释放的滤泡在琼脂糖包被的微量滴定板中悬浮培养,以防止形成单层细胞。在连续的24或36小时内,通过[3H]胸苷掺入和放射自显影来测量生长反应。即使在没有其他生长因子的情况下,胰岛素也能以浓度依赖的方式刺激[3H]胸苷掺入,在8微克/毫升时,从基础水平的486±(标准误)18 cpm升至4222±367 cpm/5×10(4)个细胞。相比之下,单独的促甲状腺激素没有作用。然而,在存在阈值水平(0.08微克/毫升)胰岛素的情况下,对促甲状腺激素有高度显著(P<0.001)的反应,[3H]胸苷掺入从无促甲状腺激素时的1089±163 cpm升至1毫单位/毫升促甲状腺激素时的最高7548±585 cpm。在测试的浓度范围内,胰岛素和促甲状腺激素之间存在协同相互作用。单独或与胰岛素联合使用的表皮生长因子均未产生显著反应。平行的放射自显影研究与[3H]胸苷掺入数据一致。我们得出结论,在没有其他生长因子的情况下,促甲状腺激素无法刺激分离的大鼠甲状腺滤泡中的DNA合成,但仅加入单一生长因子胰岛素就能产生显著反应。这些观察结果强调了在评估可疑组织特异性有丝分裂原的体外作用时,需要加入适当的允许性生长因子。

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