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Tissue kallikrein protects SH‐SY5Y neuronal cells against oxygen and glucose deprivation‐induced injury through bradykinin B2 receptor‐dependent regulation of autophagy induction
Author(s) -
Liu Yanping,
Lu Zhengyu,
Cui Mei,
Yang Qi,
Tang Yuping,
Dong Qiang
Publication year - 2016
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/jnc.13690
Subject(s) - autophagy , protein kinase a , neuroprotection , ampk , pi3k/akt/mtor pathway , mapk/erk pathway , microbiology and biotechnology , sh sy5y , gene knockdown , chemistry , biology , kinase , signal transduction , apoptosis , pharmacology , cell culture , biochemistry , neuroblastoma , genetics
Previous studies have demonstrated that tissue kallikrein ( TK ) protects against cerebral ischemia injury mainly through inhibition of apoptosis via bradykinin B2 receptor (B2R). In this study, we proposed that autophagy induction contributed to the neuroprotective mechanism of TK . To validate this hypothesis, we investigated TK ‐induced autophagy and its signaling mechanisms in human SH ‐ SY 5Y cells exposed to oxygen and glucose deprivation ( OGD ). We found that TK treatment enhanced autophagy induction, reflected by augmented LC 3 conversion and Beclin1 expression, decreased p62 levels and increased monomeric red fluorescent protein‐ LC 3 puncta formation. Green fluorescent protein‐monomeric red fluorescent protein‐ LC 3 adenovirus assay indicated that TK maintained autophagic flux. Moreover, bafilomycin A1 (Baf.A1) caused obvious LC 3‐ II accumulation either in the presence or absence of TK . Autophagy inhibition by Beclin1 knockdown or Baf.A1 treatment abrogated the neuroprotective effects of TK . Mitogen‐activated protein kinase kinase 1/2 (MEK1/2)/extracellular signal‐regulated kinase ( ERK )1/2 and AMP‐activated protein kinase ( AMPK )/tuberous sclerosis complex 2 ( TSC 2)/mammalian target of rapamycin ( mTOR ) signaling were induced by OGD stress and enhanced by TK . MEK / ERK inhibitor U0126 alone elevated autophagy in OGD conditions, but impaired TK ‐induced autophagy. Blockade of AMPK / TSC 2/ mTOR signaling by AMPK inhibitor compound C and sh RNA mediated the knockdown of AMPK α1 and TSC 2 but abolished autophagy in SH ‐ SY 5Y cells exposed to OGD treated either with or without TK . Moreover, B2R expression was up‐regulated by OGD exposure. B2R knockdown attenuated autophagy and suppressed MEK 1/2/ ERK 1/2 and AMPK / TSC 2/ mTOR signaling in OGD conditions in either the presence or absence of TK . In sum, we revealed the significance of B2R‐mediated MEK / ERK and AMPK signaling in autophagy induction under OGD stress, and proposed novel mechanisms involved in the neuropotective function of TK through B2R‐dependent regulation of autophagy.We propose the depicted model for the neuroprotective mechanism of tissue kallikrein (TK) during OGD stress: TK enhances bradykinin B2 receptor (B2R)‐mediated MEK1/2/ERK1/2 and AMPK/TSC2/mTOR signaling, thus inducing protective autophagy. The findings reported in this study should provide new evidence for the pro‐survival role of B2R‐mediated autophagy in cerebral ischemia.