Literature DB >> 6370669

Insulin receptors in isolated adult mouse intestinal cells: studies in vivo and in organ culture.

N Gallo-Payet, J S Hugon.   

Abstract

Isolated intestinal cells from adult mice possess a high concentration of insulin receptors. The binding capacity and the number of binding sites are higher in duodenum than in jejunum or ileum and in the upper part of the villus than in the crypts. The specific binding is, respectively, 11.8 +/- 1.0%, 9.1 +/- 4.0%, and 5.5 +/- 0.3%/mg . protein for duodenum, jejunum, and ileum. The number of high affinity sites per cell is, respectively, 11.0 X 10(3), 3 X 10(3), and 2.5 X 10(3). The number of low affinity sites per cell is, respectively, 11.0 X 10(4), 4.1 X 10(3), and 3.9 X 10(3). This specific binding increases to 15.9 +/- 0.9% after 24 h of fasting and to 24.5 +/- 2.2% mg protein after 48 h of fasting. This increase is due not only to an increment in the number of sites but also to alterations in affinity constants (K1, control, 0.380, 48-h fasting, 0.044 X 10(9) M-1; K2, control, 1.20, 48-h fasting; 2.61 X 10(7) M-1). The receptors are mainly located on the basolateral and internal membranes (P1, 9.4 +/- 0.7%/mg protein), but are also present on brush border membranes (P2, 2.6 +/- 1.1%/mg protein, P less than 0.01). After 24 h of organ culture, the specific binding is not modified in duodenal explants. Moreover, in the presence of insulin in the culture medium, the binding is decreased by 59%.

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Year:  1984        PMID: 6370669     DOI: 10.1210/endo-114-5-1885

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  18 in total

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4.  A low-temperature method for the isolation of small-intestinal epithelium along the crypt-villus axis.

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6.  Effects of intestinal adaptation on insulin binding to villus cell membranes.

Authors:  G P Young; C L Morton; I S Rose; T M Taranto; P S Bhathal
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9.  Organ culture of chicken cecum: morphologic and physiologic observations after 24 and 48 h of culture.

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10.  Insulin, IGF-1, and IGF-2 receptors in rat small intestine following massive small bowel resection. Analysis by binding, flow cytometry, and immunohistochemistry.

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