Intracellular pH regulation in rat round spermatids
Author
dc.contributor.author
Osses, Nelson
Author
dc.contributor.author
Pancetti, Floria
Author
dc.contributor.author
Benos, Dale J.
Author
dc.contributor.author
Reyes, Juan G.
Admission date
dc.date.accessioned
2019-01-29T17:15:43Z
Available date
dc.date.available
2019-01-29T17:15:43Z
Publication date
dc.date.issued
1997
Cita de ítem
dc.identifier.citation
Biology of the Cell, Volumen 89, Issue 4, 2018, Pages 273-283
Identifier
dc.identifier.issn
02484900
Identifier
dc.identifier.other
10.1016/S0248-4900(97)82315-5
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/163318
Abstract
dc.description.abstract
Intracellular pH has been shown to be an important physiological parameter in cell cycle control and differentiation, aspects that are central to the spermatogenic process. However, the pH regulatory mechanisms in spermatogenic cells have not been systematically explored. In this work, measuring intracellular pH (pH(i)) with a fluorescent probe (BCECF), membrane potential with a fluorescent lipophilic anion (bisoxonol), and net movement of acid using a pH-stat system, we have found that rat round spermatids regulate pH(i) by means of a V-type H+-ATPase, a HCO3- entry pathway, a Na+/HCO3- dependent transport system, and a putative proton conductive pathway. Rat spermatids do not have functional base extruder transport systems. These pH regulatory characteristics seem specially designed to withstand acid challenges, and can generate sustained alkalinization upon acid exit stimulation.