[Effects of histamine on proliferation, apoptosis and differentiation of human keratinocytes].

Li-wei Ran, Wei-ming Tan, Sheng-shun Tan, Ru Zhang, Wan-juan Wang
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Abstract

Objective: To investigate the effects of histamine on the proliferation, apoptosis and differentiation of human keratinocytes (HKC) and the mechanisms.

Methods: The effect of histamine on the growth of HKC in vitro was examined by MTT assay and trypan blue exclusion assay. Cell cycle analysis and early apoptosis analysis by double staining with Annexin V-FITC and PI were carried out by flow cytometry. DNA ladder assay was performed for the detection of cell apoptosis. HKC free calcium concentration ([Ca(2+)](i)) was measured by laser scanning confocal microscopy in combination with calcium fluorescence probe Fluo-3/AM. HKC differentiation markers keratin 10 (K10) and involucrin was detected by streptavidinbiotin complex immunocytochemical assay.

Results: Histamine at high concentration inhibited the proliferation of HKC with cell viability ratio of 65.6% at 1 x 10(-4) mol/L, while histamine at low concentrations promoted proliferation of HKC with the cell viability ratio of 130.7% at 1 x 10(-8) mol/L. Histamine at 1 x 10(-4) mol/L altered cell cycle distribution of HKC with an increase in G0/G1-phase cell population to 30.97%, a decrease in S-phase population to 73.81% and inhibition of G1/S switching. Histamine at 1 x 10(-4) mol/L induced obvious apoptosis of HKC with early apoptosis ratio of 18.64% as compared with the control (5.60%, P<0.05). Histamine 1 x 10(-4) mol/L induced an increase of HKC [Ca(2+)](i) up to 58.9% and cimetidine (an H(2) receptor antagonist) decreased HKC [Ca(2+)](i) down to 25.4%. Histamine at this concentration down-regulated the expressions of K10 and involucrin of HKC but these changes were not significantly different from those of the control (P>0.05).

Conclusions: Histamine at high concentrations inhibits cell cycle progress of HKC, mediates cell apoptosis and induces the increase of [Ca(2+)](i), which might be a partial explanation for growth arrest of HKC elicited by histamine. Histamine may regulate epidermal tissue turnover under physiological conditions, whereas under pathological circumstances of the skin as in trauma and inflammation, histamine at high concentrations may inhibit the regeneration of epidermis and the differentiation of HKC.

组胺对人角质形成细胞增殖、凋亡和分化的影响。
目的:探讨组胺对人角质形成细胞(HKC)增殖、凋亡和分化的影响及其机制。方法:采用MTT法和台盼蓝法检测组胺对体外培养的HKC细胞生长的影响。流式细胞术采用Annexin V-FITC和PI双染色法分析细胞周期和早期凋亡。采用DNA阶梯法检测细胞凋亡。用激光扫描共聚焦显微镜联合钙荧光探针Fluo-3/AM测定HKC游离钙浓度([Ca(2+)](i))。采用链亲和素复合免疫细胞化学法检测HKC分化标志物角蛋白10 (K10)和天花素(involucrin)。结果:高浓度组胺在1 × 10(-4) mol/L下抑制HKC增殖,细胞活力比为65.6%;低浓度组胺在1 × 10(-8) mol/L下促进HKC增殖,细胞活力比为130.7%。1 × 10(-4) mol/L组胺改变HKC细胞周期分布,G0/G1期细胞数量增加至30.97%,S期细胞数量减少至73.81%,G1/S转换受到抑制。1 × 10(-4) mol/L组胺诱导HKC明显凋亡,早期凋亡率为18.64%,高于对照组(5.60%,P0.05)。结论:高浓度组胺抑制HKC细胞周期进程,介导细胞凋亡,诱导[Ca(2+)](i)升高,这可能是组胺引起HKC生长阻滞的部分原因。在生理条件下,组胺可以调节表皮组织的更新,而在皮肤的病理情况下,如创伤和炎症,高浓度组胺可能会抑制表皮的再生和HKC的分化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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