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肺表面活性物质相关蛋白A研究进展 2

来源:医学杂志 2006-08-06 10:06:30 

用对Ⅱ型细胞增殖影响明显[15]。促分泌素通过 增大Ⅱ型细胞表面的SP-A受体密度从而增加SP-A的结合位点[4]。Shannon等的研 究表明细胞骨架能稳定SP mRNA,如用细胞松弛素、秋水仙碱处理Ⅱ型细胞,SP-A mRNA的 半衰期受到影响,SP-A合成量下降。Griffin发现Ⅱ型细胞与纤维母细胞共同培养时可分泌 胰岛素样生长因子-1(IGF-1)来刺激纤维母细胞胶原-Ⅰ分泌,后者对Ⅱ型细胞的营养作 用使SP-A mRNA表达上升[7]。

  尽管目前关于SP-A合成调控的研究很多,但到目前,SP-A的基因转录调控机制还尚未 完全阐明。

  4 SP-A的临床意义

  羊水中SP-A可判断胎肺发育情况;SP-A可用于评价肺气血屏障完整性,也可作为检测 肺分泌细胞变化的外周标志[3]。SP-A与许多肺疾病密切相关,它可作为诊断肺腺 癌的特异性标记物[10];SP-A与ARDS严重程度呈负相关,SP-A含量下降可作为AR DS敏感标志,甚至可作为急性肺损伤高危患者预警和预后指标。同时,因SP-A的含量变化 先于X胸片改变,故它可用于肺疾病疗效监测[2]。SP-A与肺炎、肺泡蛋白沉着症 结节病、过敏性肺泡炎、特发性肺间质纤维化和支气管哮喘等疾病的发病有关。新生儿ARDS 、支气管发育不良、慢性肺损伤等则可能与SP-A缺陷有关。

  综上所述,SP-A功能、分泌调节复杂,临床意义重大,同时,PS替代疗法已初步取得 较好的临床效果,因此SP-A的制备和临床大规模应用成为未来的研究方向。

  作者简介:郝嘉,男,26岁,住院医师,硕士研究生

  作者单位:(第三军医大学附属新桥医院心血管外科) 重庆,400037

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