TY - JOUR
T1 - G protein-coupled receptors (GPCRs) in Alzheimer's disease
T2 - A focus on BACE1 related GPCRs
AU - Zhao, Juan
AU - Deng, Yulin
AU - Jiang, Zhaotan
AU - Qing, Hong
N1 - Publisher Copyright:
© 2016 Zhao, Deng, Jiang and Qing.
PY - 2016/3/24
Y1 - 2016/3/24
N2 - The G protein coupled receptors (GPCRs) have been considered as one of the largest families of validated drug targets, which involve in almost overall physiological functions and pathological processes. Meanwhile, Alzheimer's disease (AD), the most common type of dementia, affects thinking, learning, memory and behavior of elderly people, that has become the hotspot nowadays for its increasing risks and incurability. The above fields have been intensively studied, and the link between the two has been demonstrated, whereas the way how GPCRs perturb AD progress are yet to be further explored given their complexities. In this review, we summarized recent progress regarding the GPCRs interacted with β-site APP cleaving enzyme 1 (BACE1), a key secretase in AD pathogenesis. Then we discussed the current findings on the regulatory roles of GPCRs on BACE1, and the possibility for pharmaceutical treatment of AD patients by the allosteric modulators and biased ligands of GPCRs. We hope this review can provide new insights into the understanding of mechanistic link between GPCRs and BACE1, and highlight the potential of GPCRs as therapeutic target for AD.
AB - The G protein coupled receptors (GPCRs) have been considered as one of the largest families of validated drug targets, which involve in almost overall physiological functions and pathological processes. Meanwhile, Alzheimer's disease (AD), the most common type of dementia, affects thinking, learning, memory and behavior of elderly people, that has become the hotspot nowadays for its increasing risks and incurability. The above fields have been intensively studied, and the link between the two has been demonstrated, whereas the way how GPCRs perturb AD progress are yet to be further explored given their complexities. In this review, we summarized recent progress regarding the GPCRs interacted with β-site APP cleaving enzyme 1 (BACE1), a key secretase in AD pathogenesis. Then we discussed the current findings on the regulatory roles of GPCRs on BACE1, and the possibility for pharmaceutical treatment of AD patients by the allosteric modulators and biased ligands of GPCRs. We hope this review can provide new insights into the understanding of mechanistic link between GPCRs and BACE1, and highlight the potential of GPCRs as therapeutic target for AD.
KW - Allosteric modulator
KW - Alzheimer's disease (AD)
KW - Biased ligand
KW - G protein-coupled protein (GPCR)
KW - β-site APP cleaving enzyme 1 (BACE1)
UR - http://www.scopus.com/inward/record.url?scp=84964649219&partnerID=8YFLogxK
U2 - 10.3389/fnagi.2016.00058
DO - 10.3389/fnagi.2016.00058
M3 - Review article
AN - SCOPUS:84964649219
SN - 1663-4365
VL - 8
JO - Frontiers in Aging Neuroscience
JF - Frontiers in Aging Neuroscience
IS - MAR
M1 - 58
ER -