Leech C A, Holz G G, Habener J F
Laboratory of Molecular Endocrinology, Howard Hughes Medical Institute, Harvard Medical School, Massachusetts General Hospital, Boston 02114.
Endocrinology. 1995 Apr;136(4):1530-6. doi: 10.1210/endo.136.4.7895663.
The secretion of insulin by pancreatic beta-cells is controlled by synergistic interactions of glucose and hormones of the glucagon-related peptide family, of which pituitary adenylate cyclase-activating polypeptide (PACAP) is a member. Here we show by simultaneous recording of intracellular calcium ion ([Ca2+]i) and membrane potential that both PACAP-27 and PACAP-38 depolarize HIT-T15 cells and raise [Ca2+]i. PACAP stimulation can result in membrane depolarization by two distinct mechanisms: 1) PACAP reduces the membrane conductance and increases membrane excitability; and 2) PACAP activates a pronounced inward current that is predominantly a Na+ current, blockade by La3+, and which exhibits a reversal potential of about -28 mV. Activation of this current does not require membrane depolarization, because the response is observed when cells are held under voltage clamp at -70 mV. This current may result from the cAMP-dependent activation of nonspecific cation channels because the current is also observed in response to forskolin or membrane-permeant analogs of cAMP. We also suggest that PACAP raises [Ca2+]i and stimulates insulin secretion by three distinct mechanisms: 1) depolarization activates Ca2+ influx through L-type voltage-dependent calcium channels, 2) mobilization of intracellular Ca2+ stores, and 3) entry of Ca2+ via voltage-independent Ca2+ channels. These effects of PACAP may play an important role in a neuro-entero-endocrine loop regulating insulin secretion from pancreatic beta-cells during the transition period from fasting to feeding.
胰腺β细胞分泌胰岛素受葡萄糖与胰高血糖素相关肽家族激素的协同相互作用控制,垂体腺苷酸环化酶激活多肽(PACAP)是该家族的一员。在此,我们通过同时记录细胞内钙离子浓度([Ca2+]i)和膜电位发现,PACAP - 27和PACAP - 38均可使HIT - T15细胞去极化并升高[Ca2+]i。PACAP刺激可通过两种不同机制导致膜去极化:1)PACAP降低膜电导并增加膜兴奋性;2)PACAP激活一种明显的内向电流,该电流主要为Na+电流,可被La3+阻断,其反转电位约为 - 28 mV。这种电流的激活不需要膜去极化,因为在电压钳制于 - 70 mV时可观察到该反应。这种电流可能源于cAMP依赖性激活非特异性阳离子通道,因为在对福斯可林或cAMP的膜渗透性类似物的反应中也可观察到该电流。我们还认为,PACAP通过三种不同机制升高[Ca2+]i并刺激胰岛素分泌:1)去极化激活L型电压依赖性钙通道的Ca2+内流;2)动员细胞内Ca2+储存;3)通过电压非依赖性Ca2+通道使Ca2+内流。在从禁食到进食的过渡期,PACAP的这些作用可能在调节胰腺β细胞胰岛素分泌的神经 - 肠 - 内分泌环路中发挥重要作用。