首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Binding and biological effects of tumor necrosis factor alpha on cultured human neonatal foreskin keratinocytes.
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Binding and biological effects of tumor necrosis factor alpha on cultured human neonatal foreskin keratinocytes.

机译:肿瘤坏死因子α对培养的人新生儿包皮角质形成细胞的结合和生物学作用。

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摘要

Tumor necrosis factor alpha (TNF alpha) localizes to the epidermis when injected in vivo, but its role in the skin has heretofore not been evaluated. As a first approach to assessing the role of TNF alpha in the skin, we evaluated the binding and biological effects of TNF alpha on human neonatal foreskin keratinocytes maintained in culture. We found that TNF alpha at 0.3-1.0 nM inhibited proliferation of keratinocytes in a reversible fashion as demonstrated by a reduction in total DNA content and clonal growth. The antiproliferative effects were most marked when TNF alpha was added in the preconfluent stages of cell growth. Accompanying this antiproliferative effect was a stimulation by TNF alpha of differentiation of keratinocytes as indicated by the stimulation of cornified envelope formation. Keratinocytes specifically bound TNF alpha, reaching maximal binding in 2 h at 34 degrees C or 8 h at 4 degrees C. Much of the apparent binding at 34 degrees C was due to internalization of the TNF alpha. At 4 degrees C the rate of internalization was much less. Confluent keratinocytes showed a single class of high-affinity receptors with 1,250 receptors/cell and a Kd of 0.28 nM. These data suggest a role for TNF alpha in the growth and differentiation of the epidermis.
机译:当体内注射时,肿瘤坏死因子α(TNFα)定位于表皮,但是迄今为止尚未评估其在皮肤中的作用。作为评估TNFα在皮肤中的作用的第一种方法,我们评估了TNFα对培养物中维持的人类新生儿包皮角质形成细胞的结合和生物学作用。我们发现,TNF-α在0.3-1.0 nM之间以可逆的方式抑制了角质形成细胞的增殖,这可通过减少总DNA含量和克隆生长来证明。当在细胞生长的融合前阶段添加TNFα时,抗增殖作用最为明显。伴随这种抗增殖作用的是由TNFα刺激的角质形成细胞分化,如对角质化包膜形成的刺激所示。角质形成细胞特异性结合TNFα,在34℃下2小时或在4℃下8小时达到最大结合。在34℃下的许多表观结合是由于TNFα的内在化。在4摄氏度时,内在化的速度要小得多。融合的角质形成细胞显示出一类高亲和力受体,每细胞具有1,250个受体,Kd为0.28 nM。这些数据表明TNFα在表皮的生长和分化中的作用。

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