HOMOLOGOUS BUT NOT HETEROLOGOUS CONTACT INCREASES THE INSULIN-SECRETION OF INDIVIDUAL PANCREATIC B-CELLS
HOMOLOGOUS BUT NOT HETEROLOGOUS CONTACT INCREASES THE INSULIN-SECRETION OF INDIVIDUAL PANCREATIC B-CELLS
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DOI:
10.1016/0014-4827(89)90365-0
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发表时间:
1989-09-01
影响因子:
3.7
通讯作者:
MEDA, P
中科院分区:
文献类型:
--
作者:
BOSCO, D;ORCI, L;MEDA, P
To assess whether and how specifically contact influences the functioning of differentiated cells, we have studied the secretion of adult pancreactic B-cells as a function of aggregation to either homologous B-cells or other heterologous endocrine islet cell types, all present in a mixed cell suspension. Using an immunological plaque assay for insulin, we have quantitated the proportion of single and aggregated B-cells inducing the formation of a hemolytic plaque (a reflection of the size of the secreting cell population) and the area of these plaques (a reflection of the hormonal output of individual cells or aggregates) after a 30-min stimulation by 16.7 mM glucose. By taking into account the number of B-cells within the aggregates, we have calculated from these data the insulin output on a per B-cell basis. We show here that the homologous contact between companion B-cells promotes the recruitment of secreting B-cells and increases theier individual secretion of insulin twofold over that of single B-cells. By contrast, heterologous B- to non-B-cell contact was not effective in enhancing the recruitment of secreting B-cells and in promoting their individual secretion. These findins show that a highly differentiated cell function, such as insulin secretion, is controlled specifically by homologous cell to cell contacts.