摘要
目的 探讨增生性瘢痕和自身对照正常处皮肤中应激活化蛋白激酶 (SAPK)及其上游信号分子MAPKs(MKK4和 MKK7)基因表达的变化。 方法 提取 8例增生性瘢痕和自身对照正常处皮肤组织的总 RNA后 ,分离纯化 m RNA,用 RT- PCR方法检测 SAPK,MKK4和 MKK7基因在不同组织中的表达变化规律。 结果 增生性瘢痕中 ,MKK7和 SAPK基因表达较弱 ,自身对照皮肤组织中 ,这两种基因 PCR结果的灰度比分别为增生性瘢痕的 1.5倍和 2 .6倍 ,基因表达量明显升高 (P<0 .0 1) ,而 MKK4在这两种不同类型组织中的表达量无统计学意义 (P>0 .0 5 )。 结论 增生性瘢痕中 MKK7和 SAPK基因表达降低引起细胞凋亡减少 ,可能是瘢痕内成纤维细胞大量增殖 ,增生性瘢痕形成的机制之一。
Objective To explore the change of gene expression of stress activated protein kinase (SAPK) and its upstream signal-regulated molecule ——mitogen activated protein kinases(MAPKs) (MKK4 and MKK7) in hypertrophic scar and auto-control normal skin. Methods The total RNA was isolated from 8 hypertrophic scars and 8 auto-control skin, and then mRNA was purified. The gene expressions of MKK4, MKK7 and SAPK were examined with reverse transcription-polymerase chain reaction(RT-PCR) method. Results In hypertrophic scar, both MKK7 and SAPK genes weakly expressed. In auto-control skin, the expression of these 2 genes was significantly elevated in comparison with hypertrophic scar (P<0.01). The expression levels of these 2 genes were 1.5 times and 2.6 times as long as those of hypertrophic scar, respectively. Gene expression of MKK4 had no significant difference between auto-control skin and hypertrophic scar (P>0.05). Conclusion Decreased gene expression of MKK7 and SAPK which results in reducing cell apoptosis might be one of the mechanisms for controlling the formation of hypertrophic scar.
出处
《中国修复重建外科杂志》
CAS
CSCD
2004年第1期1-3,共3页
Chinese Journal of Reparative and Reconstructive Surgery
基金
国家重点基础研究发展规划项目(973):创伤愈合与组织修复的分子基础研究基金资助项目(G1999054204)
国家杰出青年科学基金资助项目(39525024)
国家自然科学基金资助项目(39870731) ~~