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促肾上腺皮质激素释放肽可使空肠绒毛肠上皮细胞内硝苯地平敏感的容量减少。

Corticostatic peptides cause nifedipine-sensitive volume reduction in jejunal villus enterocytes.

作者信息

MacLeod R J, Hamilton J R, Bateman A, Belcourt D, Hu J, Bennett H P, Solomon S

机构信息

Department of Pediatrics, McGill University-Montreal Children's Hospital Research Institute, Quebec, Canada.

出版信息

Proc Natl Acad Sci U S A. 1991 Jan 15;88(2):552-6. doi: 10.1073/pnas.88.2.552.

Abstract

We studied cell-volume changes caused by adding corticostatin (CS) or defensin-like peptides to villus enterocytes isolated in suspension from guinea pig jejunum. Guinea pig CS (10(-9) M) added to villus cells in Na(+)-containing medium reduced volume, but immediate cell swelling was caused by 10(-6) M guinea pig CS. In Na(+)-free N-methyl-D-glucamine-containing medium 10(-9) M guinea pig CS accelerated the initial rate of shrinkage compared with cells in N-methyl-D-glucamine-containing medium alone as well as causing greater cell shrinkage. Guinea pig CS-stimulated cell shrinkage was prevented by a Ca2(+)-channel blocker--5 microM nifedipine, by chelation of extracellular Ca2+ with 100 microM EGTA, or by omega-conotoxin (10(-9) M). The Ca2+ ionophore A23187 (2.5 microM) reduced volume when added to villus cells in N-methyl-D-glucamine-containing medium; this action was prevented by EGTA, or quinine--an inhibitor of K+ conductance, or 9-anthracenecarboxylic acid--a Cl- channel blocker, suggesting that the volume reduction occurred because K+ and Cl- conductances were activated. Guinea pig CS-stimulated volume reduction was also prevented by 100 microM quinine or 9-anthracenecarboxylic acid. We conclude that jejunal villus enterocytes possess a Ca2(+)-activated Cl- conductance and a K+ conductance that need not be stretch-activated. Corticostatic peptides cause volume reduction in villus cells by activating L-type Ca2+ channels; other defensin-like peptides were without effect.

摘要

我们研究了向从豚鼠空肠中分离出的悬浮绒毛肠上皮细胞添加皮质抑素(CS)或防御素样肽所引起的细胞体积变化。在含钠培养基中向绒毛细胞添加10⁻⁹ M的豚鼠CS会使细胞体积减小,但10⁻⁶ M的豚鼠CS会导致细胞立即肿胀。在不含钠的含N - 甲基 - D - 葡糖胺的培养基中,与仅含N - 甲基 - D - 葡糖胺的培养基中的细胞相比,10⁻⁹ M的豚鼠CS加快了初始收缩速率,并且导致更大程度的细胞收缩。豚鼠CS刺激的细胞收缩可被Ca²⁺通道阻滞剂——5 μM硝苯地平、用100 μM乙二醇双(氨基乙基醚)四乙酸(EGTA)螯合细胞外Ca²⁺或ω - 芋螺毒素(10⁻⁹ M)所阻止。当向含N - 甲基 - D - 葡糖胺的培养基中的绒毛细胞添加Ca²⁺离子载体A23187(2.5 μM)时,细胞体积减小;EGTA、K⁺电导抑制剂奎宁或Cl⁻通道阻滞剂9 - 蒽甲酸可阻止这种作用,这表明体积减小是因为K⁺和Cl⁻电导被激活。100 μM奎宁或9 - 蒽甲酸也可阻止豚鼠CS刺激的体积减小。我们得出结论,空肠绒毛肠上皮细胞具有一种Ca²⁺激活的Cl⁻电导和一种无需拉伸激活的K⁺电导。皮质抑制肽通过激活L型Ca²⁺通道导致绒毛细胞体积减小;其他防御素样肽则无此作用。

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