首页> 外文期刊>Regulatory peptides. >Endogenous adrenomedullin system regulates the growth of rat adrenocortical cells cultured in vitro.
【24h】

Endogenous adrenomedullin system regulates the growth of rat adrenocortical cells cultured in vitro.

机译:内源性肾上腺髓质素系统调节体外培养的大鼠肾上腺皮质细胞的生长。

获取原文
获取原文并翻译 | 示例
           

摘要

The expression of adrenomedullin (AM) system (AM and its receptors), as mRNA and protein, has been detected in the mammalian adrenal zona glomerulosa (ZG) cells. Evidence has been also provided that exogenous AM is able to enhance in vivo and in vitro the proliferative activity of ZG cells. However, the possibility that endogenous AM system may act as a physiological ZG growth regulator has not yet been demonstrated. Hence, we investigated whether the prolonged (48-72 h) suppression of AM gene transcription by a specific antisense oligonucleotide or the long-lasting (24-96 h) blockade of AM receptors by the selective antagonist AM(22-52) are able to affect the growth of rat ZG cells cultured in vitro. Freshly dispersed cells were incubated for 3 h with an AM antisense or a scrambled oligonucleotide, then they were cultured for 48 or 72 h, and proAM mRNA expression and AM content was checked by reverse transcription-polymerase chain reaction and radioimmune assay, respectively. Other ZG cells were cultured in the presence of AM and/or AM(22-52). Growth assay showed that AM (10(-8) M) decreased and AM(22-52) (10(-6) M) increased the duplication time of cultured cells. AM (10(-8) M) raised proliferation index and decreased apoptotic index of cultured cells, and AM(22-52) reversed these effects. AM(22-52) (from 10(-7) to 10(-6) M) and pAM gene suppression by the antisense oligonucleotide significantly lowered proliferation index and increased apoptotic index of cultured cells, both these effects being abrogated by AM (10(-8) M). It is concluded that endogenous AM system plays a relevant role in the autocrine-paracrine regulation of cultured rat ZG-cell growth.
机译:在哺乳动物肾上腺肾小球(ZG)细胞中已检测到肾上腺髓质素(AM)系统(AM及其受体)的mRNA和蛋白质表达。还提供了外源AM能够增强体内和体外ZG细胞增殖活性的证据。但是,尚未证明内源性AM系统可以充当生理ZG生长调节剂的可能性。因此,我们研究了通过特异性反义寡核苷酸对AM基因转录的长时间抑制(48-72 h)或选择性拮抗剂AM(22-52)对AM受体的持久抑制(24-96 h)是否能够影响体外培养的大鼠ZG细胞的生长。将新鲜分散的细胞与AM反义或加扰的寡核苷酸孵育3小时,然后培养48或72小时,分别通过逆转录聚合酶链反应和放射免疫法检查proAM mRNA表达和AM含量。在AM和/或AM(22-52)存在下培养其他ZG细胞。生长试验表明,AM(10(-8)M)减少,AM(22-52)(10(-6)M)增加培养细胞的复制时间。 AM(10(-8)M)提高培养细胞的增殖指数,降低其凋亡指数,而AM(22-52)则逆转了这些作用。 AM(22-52)(从10(-7)到10(-6)M)和反义寡核苷酸对pAM基因的抑制作用显着降低了培养细胞的增殖指数并提高了细胞的凋亡指数,而这两种作用均被AM消除(10 (-8)M)。结论是内源性AM系统在培养大鼠ZG细胞生长的自分泌-旁分泌调节中起着相关作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号