Tetanus toxin-mediated cleavage of cellubrevin inhibits proton secretion in the male reproductive tract (CROSBI ID 86061)
Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija
Podaci o odgovornosti
Breton, Sylvie ; Nsumu, Ndona N. ; Thierry, Galli ; Sabolić, Ivan ; Smith, Peter J.S. ; Brown, Dennis
engleski
Tetanus toxin-mediated cleavage of cellubrevin inhibits proton secretion in the male reproductive tract
Our laboratory has previously shown that the vacuolar H+-ATPase, located in a subpopulation of specialized cells establishes a luminal acidic environment in the epididymis and proximal part of the vas deferens (Breton S, Smith PSJ, Lui B, and Brown D. Nat Med 2:470-472, 1996). Low luminal pH is critical for sperm maturation and maintainance of sperm in a quiescent state during storage in these organs. In the present study we examined the regulation of proton secretion in the epididymis and vas deferens. In vivo microtubule disruption by colchicine induced an almost complete loss of H+-ATPase apical polarity. Endocytotic vesicles, visualized by Texas red-dextran internalization, contain H+-ATPase, indicating active endocytosis of the pump. Cellubrevin, an analog of the vesicle soluble N-ethyl maleimide-sensitive factor attachment protein (SNAP) receptor (v-SNARE) synaptobrevin, is highly enriched in H+-ATPase- rich cells of the epididymis and vas deferens, and tetanus toxin treatment markedly inhibited bafilomycin-sensitive proton secretion by 64.3 ą 9.0% in the proximal vas deferens. Western blotting showed effective cleavage of cellubrevin by tetanus toxin in intact vas deferens, demonstrating that the toxin gained access to cellubrevin in. These results suggest that H+- ATPase is actively endocytosed and exocytosed in proton-secreting cells of the epididymis and vas deferens and that net proton secretion requires the participation of the v-SNARE cellubrevin.
vas deferens ; epididymis ; hydrogen-adenosine 3'5'-triphosphatase ; vesicle endocytosis ; soluble N-ethyl maleimide-sensitive factor for attachment protein receptors
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Podaci o izdanju
278 (5)
2000.
F717-F725
objavljeno
1931-857X
1522-1466
10.1152/ajprenal.2000.278.5.F717
Povezanost rada
Temeljne medicinske znanosti