AMYLOID PRECURSOR PROTEIN SECRETION VIA MUSCARINIC RECEPTORS - REDUCED DESENSITIZATION USING THE M1-SELECTIVE AGONIST AF102B

被引:44
作者
HARING, R
GURWITZ, D
BARG, J
PINKASKRAMARSKI, R
HELDMAN, E
PITTEL, Z
WENGIER, A
MESHULAM, H
MARCIANO, D
KARTON, Y
FISHER, A
机构
[1] ISRAEL INST BIOL RES,IL-74100 NESS ZIONA,ISRAEL
[2] TEL AVIV UNIV,WOLFSON MED CTR,SCH MED,IL-58100 HOLON,ISRAEL
[3] WEIZMANN INST SCI,IL-76100 REHOVOT,ISRAEL
关键词
D O I
10.1006/bbrc.1994.2232
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Secretion of amyloid precursor protein (APP) by cultured cells is coupled to several receptors, including mi muscarinic (m1AChR), and is associated with decreased production of beta A4 amyloid. Secreted and cell-associated APP levels were measured in m1AChR-transfected PC12 cells stimulated with the non-selective agonist carbachol or the Mi-selective agonist, AF102B. Secreted APP levels following stimulation with AF102B (5-60 min) were about half compared with carbachol. Yet, following 24 h stimulation with carbachol or AF102B, cell-associated APP levels were similarly decreased. This may be associated with a smaller reduction in APP secretion following 24 h stimulation with AF102B as compared with carbachol. AF102B may therefore have an advantage over non-selective muscarinic ligands for sustained decrease of cell-associated APP. (C) 1994 Academic Press, Inc.
引用
收藏
页码:652 / 658
页数:7
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