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12-羟基-5,8,10,14-二十碳四烯酸(12-HETE)不会刺激人新生儿角质形成细胞的增殖。

12-Hydroxy-5,8,10,14-eicosatetraenoic acid (12-HETE) does not stimulate proliferation of human neonatal keratinocytes.

作者信息

Otto W R, Barr R M, Dowd P M, Wright N A, Greaves M W

机构信息

Department of Histopathology, Royal Postgraduate Medical School, Hammersmith Hospital, London, England.

出版信息

J Invest Dermatol. 1989 May;92(5):683-8. doi: 10.1111/1523-1747.ep12696874.

Abstract

We have developed an assay to study the effect of drugs on the proliferation of neonatal human skin-derived keratinocytes in vitro. Expanding populations of neonatal keratinocytes were cultured in low concentrations (0.5%) of fetal calf serum for up to 12 d. Growth of the cultures was determined by measurement of DNA using a sensitive fluorimetric assay. Addition of 10(-9)-10(-6) M 12(RS)-hydroxy-5,8,10,14-eicosatetraenoic acid (12(RS)-HETE) neither stimulated keratinocyte proliferation nor enhanced the incorporation of [3H]thymidine. The ability of neonatal keratinocytes in low serum medium to respond to exogenous factors was demonstrated by increased growth in response to a mixture of cholera toxin, hydrocortisone, and epidermal growth factor. Confluent keratinocyte cultures in 10% human AB serum exposed to 12(S)-HETE for 72 h also showed no changes in DNA, [3H]thymidine incorporation, or labeling index. Metabolism of 12(S)-[3H]HETE was greater in cultures containing low concentrations of serum but there was no evidence for the formation of 12,20-dihydroxyeicosatetraenoic acid.

摘要

我们已经开发出一种检测方法,用于研究药物对体外培养的新生儿人皮肤来源角质形成细胞增殖的影响。将不断扩增的新生儿角质形成细胞群体在低浓度(0.5%)胎牛血清中培养长达12天。通过使用灵敏的荧光分析法测量DNA来确定培养物的生长情况。添加10⁻⁹ - 10⁻⁶ M的12(RS)-羟基-5,8,10,14-二十碳四烯酸(12(RS)-HETE)既不刺激角质形成细胞增殖,也不增强[³H]胸腺嘧啶核苷的掺入。霍乱毒素、氢化可的松和表皮生长因子的混合物可使低血清培养基中的新生儿角质形成细胞生长增加,从而证明了其对外部因子的反应能力。在10%人AB血清中汇合的角质形成细胞培养物暴露于12(S)-HETE 72小时后,DNA、[³H]胸腺嘧啶核苷掺入或标记指数也没有变化。在含有低浓度血清的培养物中,12(S)-[³H]HETE的代谢更活跃,但没有证据表明形成了12,20-二羟基二十碳四烯酸。

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