Lu Feng, Gao JianHua, Ogawa Rei, Hyakusoku Hiko
Department of Plastic and Reconstructive Surgery, Southern Medical University, Guangzhou, China.
Plast Reconstr Surg. 2007 Mar;119(3):844-51. doi: 10.1097/01.prs.0000255539.99698.f4.
Expression of connexins and other constituent proteins of gap junctions along with gap junctional intercellular communication are involved in cellular development and differentiation processes. In addition, an increasing number of hereditary skin disorders appear to be linked to connexins. Therefore, in this report, the authors studied in vitro gap junctional intercellular communication function and connexin expression in fibroblasts derived from keloid and hypertrophic scar patients.
Fibroblasts harvested from each of six keloid and hypertrophic scar patients were used for this study. Gap junctional intercellular communication function was investigated using the gap fluorescence recovery after photobleaching method, and expression of connexin proteins was studied using quantitative confocal microscopic analyses.
Compared with normal skin, a decreased level of gap junctional intercellular communication was seen in fibroblasts derived from hypertrophic scar tissue, whereas an extremely low gap junctional intercellular communication level was detected in fibroblasts derived from keloid tissue. We also detected little connexin 43 (Cx43) protein localized in fibroblasts derived from keloids. Moreover, Cx43 protein levels were much lower in fibroblasts derived from hypertrophic scars than in those derived from normal skin.
The authors' data suggest that the loss of gap junctional intercellular communication and connexin expression may affect intercellular recognition and thus break the proliferation and apoptosis balance in fibroblasts derived from keloid and hypertrophic scar tissue.
缝隙连接的连接蛋白和其他组成蛋白的表达以及缝隙连接细胞间通讯参与细胞发育和分化过程。此外,越来越多的遗传性皮肤病似乎与连接蛋白有关。因此,在本报告中,作者研究了瘢痕疙瘩和增生性瘢痕患者来源的成纤维细胞的体外缝隙连接细胞间通讯功能和连接蛋白表达。
本研究使用了从6名瘢痕疙瘩和增生性瘢痕患者身上采集的成纤维细胞。采用光漂白后缝隙荧光恢复法研究缝隙连接细胞间通讯功能,采用定量共聚焦显微镜分析研究连接蛋白的表达。
与正常皮肤相比,增生性瘢痕组织来源的成纤维细胞缝隙连接细胞间通讯水平降低,而瘢痕疙瘩组织来源的成纤维细胞缝隙连接细胞间通讯水平极低。我们还检测到瘢痕疙瘩来源的成纤维细胞中几乎没有连接蛋白43(Cx43)蛋白定位。此外,增生性瘢痕来源的成纤维细胞中Cx43蛋白水平远低于正常皮肤来源的成纤维细胞。
作者的数据表明,缝隙连接细胞间通讯和连接蛋白表达的丧失可能会影响细胞间识别,从而打破瘢痕疙瘩和增生性瘢痕组织来源的成纤维细胞的增殖和凋亡平衡。