共 48 条
Glucagon-like peptide-1 (GLP-1) diminishes neuronal degeneration and death caused by NGF deprivation by suppressing Bim induction
被引:72
作者:
Biswas, Subhas C.
[1
,2
]
Buteau, Jean
[3
,4
]
Greene, Lloyd A.
[1
,2
]
机构:
[1] Columbia Univ Coll Phys & Surg, Dept Pathol, Ctr Neurobiol & Behav, New York, NY 10032 USA
[2] Columbia Univ Coll Phys & Surg, Taub Ctr Alzheimers Dis Res, New York, NY 10032 USA
[3] Univ Laval, Dept Anat & Physiol, Quebec City, PQ G1V 4G5, Canada
[4] Ctr Rech Hop, Quebec City, PQ G1V 4G5, Canada
关键词:
neuronal apoptosis;
GLP-1;
Bim;
NGF;
D O I:
10.1007/s11064-008-9646-4
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 [生物化学与分子生物学];
081704 [应用化学];
摘要:
Glucagon-like peptide-1 (GLP-1) is a glucoincretin hormone most intensively studied for its actions on insulin secreting beta-cells. GLP-1 and its receptor are also found in brain and accumulating evidence indicates that GLP-1 has neuroprotective actions. Here, we investigated whether GLP-1 protects neuronal cells from death evoked by nerve growth factor (NGF) withdrawal. Compromised trophic factor signaling may underlie neurodegenerative diseases ranging from Alzheimer disease to diabetic neuropathies. We report that GLP-1 provides sustained protection of cultured neuronal PC12 cells and sympathetic neurons from degeneration and death caused by NGF deprivation. Past work shows that NGF deprivation induces the pro-apoptotic protein Bim which contributes to neuron death. Here, we find that GLP-1 suppresses Bim induction promoted by NGF deprivation. Thus, GLP-1 may protect neurons, at least in part, by suppressing Bim induction. Our findings support the idea that drugs that mimic or elevate GLP-1 represent potential therapeutics for neurodegenerative diseases.
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页码:1845 / 1851
页数:7
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