Mellergård P E, Siesjö B K
Laboratory for Experimental Brain Research, Lund University Hospital, Sweden.
Neuroreport. 1991 Nov;2(11):695-8. doi: 10.1097/00001756-199111000-00016.
Microspectrofluorometry was used to study the regulation of intracellular pH (pHi) in 2'-7'-bis (carboxyethyl-)-5,6-carboxyfluorescein (BCECF)-loaded astrocytes. They rapidly regulated an acid transient induced by an NH4+ prepulse. This back regulation was blocked by removal of Na+, or by addition of amiloride, but was also inhibited when extracellular pH (pHe) was lowered. Furthermore, when cells were exposed to HEPES buffer with reduced or increased pHe, pHi changed in parallel. Thus, although the cells possess an efficient H+ extrusion mechanism they fail to regulate pHi to a normal value unless pHe is held constant. The results challenge the concept of a H+ regulatory site at the internal side of the exchanger regulating pHi to a constant value.
利用显微分光荧光测定法研究了用2'-7'-双(羧乙基)-5,6-羧基荧光素(BCECF)负载的星形胶质细胞内pH(pHi)的调节。它们能快速调节由NH4+预脉冲诱导的酸性瞬变。这种反向调节可通过去除Na+或添加氨氯吡咪来阻断,但当细胞外pH(pHe)降低时也会受到抑制。此外,当细胞暴露于pHe降低或升高的HEPES缓冲液中时,pHi会平行变化。因此,尽管细胞拥有高效的H+外排机制,但除非pHe保持恒定,否则它们无法将pHi调节至正常值。这些结果对交换器内侧调节pHi至恒定值的H+调节位点的概念提出了挑战。