Evidence for further heterogeneity of the receptors for neuropeptide-Y and peptide-YY in tumor cell lines derived from neural crest.
Evidence for further heterogeneity of the receptors for neuropeptide-Y and peptide-YY in tumor cell lines derived from neural crest.
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神经嵴来源的肿瘤细胞系中神经肽-Y 和肽-YY 受体进一步异质性的证据。
DOI:
10.1210/endo.131.5.1330489
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发表时间:
1992
期刊:
影响因子:
4.8
通讯作者:
Masato Kasuga
中科院分区:
文献类型:
--
作者:
A. Inui;K. Sano;M. Miura;Y. Hirosue;M. Nakajima;M. Okita;S. Baba;Masato Kasuga
The expression and structure of the receptors for neuropeptide-Y (NPY) and peptide-YY (PYY) were studied in 16 human and rodent tumor cell lines derived from the neural crest by ligand binding and cross-linking techniques using [125I]Bolton-Hunter-NPY, [125I]PYY, and various forms of monoiodinated NPY and PYY. Although NPY-binding sites were observed in most of the tumor cells, PYY-binding sites were found only on the human neuroblastoma cell lines SMS-MSN, SMS-KAN, SK-N-MC, and MC-IXC and the human Ewing's sarcoma cell line SK-ES. The differential labeling of the NPY/PYY receptors on these cell lines suggests that the NPY/PYY receptors are more heterogeneous than previously described as the Y1, Y2, and Y3 receptor subtypes. Cross-linking studies demonstrate that the Y1 and Y2 receptors for NPY/PYY are structurally different (mol wt, 70 and 50 kilodaltons, respectively) and that the 70- and 50-kilodalton receptor proteins are coexpressed in certain tumor cell lines. This could explain at least in part why cell lines show a relative specificity for Y1/Y2 classification, observed as the inhibition by both C-terminal fragments and Y1-specific analogs on the NPY/PYY binding to membrane receptors. Collectively, the present study suggests further heterogeneity of the NPY/PYY receptors and the existence of multiple receptor proteins in the tumor cell lines derived from the neural crest.
影响因子:
4.8
作者:
Servin,AL;Rouyer-Fessard,C;Balasubramaniam,A;SaintPierre,S;Laburthe,M
通讯作者:
Laburthe,M
DOI:
--
发表时间:
1990
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
Nguyen,TD;Heintz,GG;Kaiser,LM;Staley,CA;Taylor,IL
通讯作者:
Taylor,IL