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ATP inhibits onset of exocytosis in permeabilised mast cells

机译:ATP抑制透化肥大细胞中胞吐作用的发生

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ATP is not required for exocytosis from permeabilised mast cells, and therefore there is no direct role for protein phosphorylation in the late stages of the activation pathway. We have measured the timecourse of exocytosis from permeabilised cells triggered to release hexosaminidase following addition of Ca2+ to cells equilibrated for 2 min with GTP-γ-S. If ATP is included at the time of permeabilisation, then exocytosis commences after a delay, the duration of which depends on the square root of the product [Ca2+][GTP-γ-S], and which may extend to beyond 3 min. When ATP is excluded then the maximal rate of exocytosis is established within 3 secs of completing the effector combination. These results suggest that the achievement of a new steady-state, induced by Ca2+ and GTP-γ-S, and required for exocytosis is inhibited by ATP. From this we conclude that dephosphorylation of an unknown regulator protein may comprise a step in the exocytotic pathway.
机译:ATP对透化肥大细胞的胞吐作用不是必需的,因此在激活途径的后期,蛋白磷酸化没有直接作用。我们已经测量了Ca2 +加入GTP-γ-S平衡细胞2分钟后,透化细胞触发释放己糖胺酶释放的时间。如果透化时包括了ATP,则胞吐作用会在延迟后开始,其持续时间取决于产物[Ca2 +] [GTP-γ-S]的平方根,并且可能会延长到3分钟以上。当排除ATP时,则在完成效应器组合后的3秒钟内将建立最大的胞吐速率。这些结果表明,ATP抑制了Ca2 +和GTP-γ-S诱导的胞吐作用所需的新稳态的实现。据此我们得出结论,未知调节蛋白的去磷酸化可能包括胞吐途径中的一个步骤。

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