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小鼠淋巴细胞上的血管活性肠肽受体更新迅速。

Receptors for vasoactive intestinal peptide on murine lymphocytes turn over rapidly.

作者信息

Ottaway C A

机构信息

Department of Medicine, University of Toronto, Ontario, Canada.

出版信息

J Neuroimmunol. 1992 Jun;38(3):241-53. doi: 10.1016/0165-5728(92)90017-f.

Abstract

The interaction of the neuropeptide vasoactive intestinal peptide (VIP) with its receptors on murine mesenteric lymph node lymphocytes (MLN) has been re-examined in detail. Intact MLN actively internalize surface bound VIP. The rate constants associated with the insertion of receptors at the MLN surface, the internalization of VIP occupied and unoccupied receptors and the elimination of the peptide were determined. At 37 degrees C, MLN insert approximately 140 VIP receptors cell-1 min-1 at their surface, and the rate of internalization of occupied receptors (0.23 min-1) was much greater than that of the unoccupied receptors (0.02 min-1). Exposure of MLN to non-saturating concentrations of VIP markedly altered the expression of VIP receptors at the lymphocyte surface. The rapid turnover of VIP receptors combined with the differential clearance of occupied and unoccupied receptors from the cell surface provides a mechanism by which homologous regulation of VIP receptor expression can occur on these lymphocytes.

摘要

已对神经肽血管活性肠肽(VIP)与其在小鼠肠系膜淋巴结淋巴细胞(MLN)上的受体之间的相互作用进行了详细的重新研究。完整的MLN会主动内化表面结合的VIP。测定了与MLN表面受体插入、VIP占据和未占据受体的内化以及肽消除相关的速率常数。在37℃时,MLN在其表面每分钟每细胞插入约140个VIP受体,被占据受体的内化速率(0.23分钟-1)远大于未被占据受体的内化速率(0.02分钟-1)。将MLN暴露于非饱和浓度的VIP会显著改变淋巴细胞表面VIP受体的表达。VIP受体的快速周转以及细胞表面被占据和未被占据受体的差异清除提供了一种机制,通过该机制这些淋巴细胞上可以发生VIP受体表达的同源调节。

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