Boyd A E, Bolton W E, Brinkley B R
J Cell Biol. 1982 Feb;92(2):425-34. doi: 10.1083/jcb.92.2.425.
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.
为了研究微管在胰岛素分泌中的作用,开发了一种单层培养系统。获取培养细胞以研究微管在胰岛素分泌中的作用。通过酶消化6至12周龄C57BL-KsJ小鼠的胰腺来获得培养细胞。在培养的第4天,更换培养基,添加对照或处理培养基,并频繁取样进行胰岛素测定。用抗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。虽然培养基中钙浓度的改变不影响微管模式,但培养基中无钙或无葡萄糖会抑制胰岛素分泌(P<0.001)。最佳胰岛素释放发生在钙浓度为2.5 mM时。浓度为10^(-10) M的秋水仙碱不影响微管免疫荧光模式,而浓度为1×10^(-7) M和5×10^(-7) M会减少微管数量,在用10^(-6) M秋水仙碱处理2小时的培养物中无法鉴定出微管。经过2小时的预孵育后,10^(-6) M秋水仙碱会降低在2.0或4.5 mg/ml葡萄糖时胰岛素的延长释放(P<0.02)。胰岛素的即时释放与对照平板相似,并且在没有可识别微管的培养物中也会发生。10^(-6) M光秋水仙碱不会改变微管和胰岛素分泌,去除秋水仙碱24小时后延长的胰岛素分泌恢复。这些研究表明,微管促进胰岛素的持续分泌,但激素的即时释放不需要微管。在胰岛素分泌中起重要作用的细胞外钙浓度的改变不会改变β细胞中的微管模式。