Williams J A
Cell Tissue Res. 1978 Jan 17;186(2):287-95. doi: 10.1007/BF00225538.
The effects of the Ca2 + ionophore A2317 on pancreatic amylase and lactate dehydrogenase (LDH) release, cellular electrolyte balance and ultrastructure were studied with the use of incubated pancreatic fragments. A23187 (0.3 micrometer) in the presence of Ca2 +, increased amylase release but at higher concentrations (1-10 micrometer) also increased LDH release and increased uptake of 14C-sucrose with concomitant loss of tissue K + and gain in Na +. The ultrastructure of the majority of acini appeared normal and showed depletion of zymogen granules. Microtubules and microfilaments which have been implicated in the release process were normal or increased in number. In the absence of Ca + the ionophore had no effect on secretion, cellular integrity or ultrastructure. It is concluded that A23187 in the presence of Ca2 + increases amylase release by a mechanism comparable to the terminal steps in stimulus-secretion coupling induced by physiological secretagogues. This provides further evidence that amylase release is mediated by a rise in cell Ca2 + although the mechanisms of the ionophore- and physiological secretagogue-induced rise in Ca + are probably different. High concentrations of ionophore (greater than 1 micrometer) also induce Ca2 + dependent damage in a fraction of the cells.
利用孵育的胰腺片段,研究了钙离子载体A2317对胰腺淀粉酶和乳酸脱氢酶(LDH)释放、细胞电解质平衡及超微结构的影响。在钙离子存在的情况下,A23187(0.3微米)可增加淀粉酶的释放,但在较高浓度(1 - 10微米)时,也会增加LDH的释放,并增加14C - 蔗糖的摄取,同时伴有组织钾离子的丢失和钠离子的增加。大多数腺泡的超微结构看起来正常,但显示酶原颗粒减少。与释放过程相关的微管和微丝数量正常或增加。在没有钙离子的情况下,离子载体对分泌、细胞完整性或超微结构没有影响。得出的结论是,在钙离子存在的情况下,A23187通过一种与生理促分泌剂诱导的刺激 - 分泌偶联的终末步骤相当的机制增加淀粉酶的释放。这进一步证明淀粉酶的释放是由细胞钙离子升高介导的,尽管离子载体和生理促分泌剂诱导的钙离子升高机制可能不同。高浓度的离子载体(大于1微米)也会在一部分细胞中诱导钙离子依赖性损伤。