A bi directional, saturable transport of glutathione (GSH) was found in rat liver microsomal vesicles. GSH transport could be inhibited by the anion transport blockers flufenamic acid and 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid. A part of GSH taken up by the vesicles was metabolized to glutathione disulfide (GSSG) in the lumen. Microsomal membrane was virtually nonpermeable toward GSSG; accordingly, GSSG generated in the microsomal lumen could hardly exit. Therefore, GSH transport, contrary to previous assumptions, is preferred in the endoplasmic reticulum, and GSSG entrapped and accumulated in the lumen creates the oxidized state of its redox buffer.
Banhegyi, G., Lusini, L., Puskas, F., Rossi, R., Fulceri, R., Braun, L., et al. (1999). Preferential transport of glutathione versus glutathione disulfide in rat liver microsomal vesicles. THE JOURNAL OF BIOLOGICAL CHEMISTRY, 274(18), 12213-12216 [10.1074/jbc.274.18.12213].
Preferential transport of glutathione versus glutathione disulfide in rat liver microsomal vesicles
ROSSI, RANIERI;FULCERI, ROSELLA;BENEDETTI, ANGIOLO
1999-01-01
Abstract
A bi directional, saturable transport of glutathione (GSH) was found in rat liver microsomal vesicles. GSH transport could be inhibited by the anion transport blockers flufenamic acid and 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid. A part of GSH taken up by the vesicles was metabolized to glutathione disulfide (GSSG) in the lumen. Microsomal membrane was virtually nonpermeable toward GSSG; accordingly, GSSG generated in the microsomal lumen could hardly exit. Therefore, GSH transport, contrary to previous assumptions, is preferred in the endoplasmic reticulum, and GSSG entrapped and accumulated in the lumen creates the oxidized state of its redox buffer.File | Dimensione | Formato | |
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https://hdl.handle.net/11365/19436
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