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Microtubules and beta cell function: effect of colchicine on microtubules and insulin secretion in vitro by mouse beta cells

机译:微管和β细胞功能:秋水仙碱对小鼠β细胞体外微管和胰岛素分泌的影响

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摘要

A monolayer culture system was developed to study the role of microtubules in insulin secretion. Cultured cells were obtained to study the role of microtubules in insulin secretion. Cultured cells were obtained by enzymatic digestion of pancreases from C57BL-KsJ mice 6-12 wk of age. On day 4 of culture, the medium was changed, control or treatment medium added, and frequent samples were removed for insulin assay. Microtubules and beta cells were identified by indirect immunofluorescence with monospecific antibodies to tubulin and insulin. An extensive microtubule network radiates from the perinuclear region of the beta cell to the plasma membrane. Although alterations in the calcium concentration of the medium did not affect the microtubule pattern, the absence of calcium or glucose in the medium inhibited insulin secretion (P less than 0.001). Optimum insulin release occurred at a calcium concentration of 2.5 mM. Colchicine, in concentrations of 10(-10) M, did not affect the microtubule immunofluorescent pattern, whereas concentrations of 1 and 5 x 10(-7) M decreased the number of microtubules, and microtubules could not be identified in cultures treated with 10(-6) M colchicine for 2 h. After a 2-h preincubation, the prolonged release of insulin at either 2.0 or 4.5 mg/ml of glucose was decreased by 10(-6) M colchicine (P less than 0.02). The immediate release of insulin was similar to that in control plates and occurred in cultures with no identifiable microtubules. Microtubules and insulin secretion were not altered by 10(-6) M lumicolchicine and prolonged insulin secretion recovered 24 h after removal of colchicine. These studies show that the microtubules facilitate sustained secretion of insulin but are not required for the immediate release of the hormone. Alterations in the extracellular calcium concentration which play an essential role in insulin secretion do not alter the microtubule pattern in the beta cell.
机译:开发了单层培养系统以研究微管在胰岛素分泌中的作用。获得培养的细胞以研究微管在胰岛素分泌中的作用。通过酶消化6-12周龄的C57BL-KsJ小鼠的胰腺获得培养的细胞。在培养的第4天,更换培养基,添加对照或处理培养基,并移出频繁的样品用于胰岛素测定。用针对微管蛋白和胰岛素的单特异性抗体通过间接免疫荧光鉴定微管和β细胞。广泛的微管网络从β细胞的核周区域辐射到质膜。尽管培养基中钙浓度的变化不会影响微管模式,但培养基中钙或葡萄糖的缺乏会抑制胰岛素分泌(P小于0.001)。最佳的胰岛素释放发生在钙浓度为2.5 mM时。秋水仙碱浓度为10(-10)M不会影响微管的免疫荧光模式,而浓度为1和5 x 10(-7)M的微管会减少微管的数量,并且在用10处理的培养物中无法鉴定出微管。 (-6)秋水仙碱2 h。预温育2小时后,通过10(-6)M秋水仙碱降低了2.0或4.5 mg / ml葡萄糖时胰岛素的延长释放(P小于0.02)。立即释放的胰岛素类似于对照板中的释放,并且发生在没有可识别的微管的培养物中。秋水仙碱去除后24小时,10(-6)M发光霉素不会改变微管和胰岛素的分泌,胰岛素分泌延长。这些研究表明,微管促进胰岛素的持续分泌,但不是立即释放激素所必需的。在胰岛素分泌中起重要作用的细胞外钙浓度的变化不会改变β细胞中的微管模式。

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