TY - JOUR
T1 - Intracellular trpa1 mediates ca2+ release from lysosomes in dorsal root ganglion neurons
AU - Shang, Shujiang
AU - Zhu, Feipeng
AU - Liu, Bin
AU - Chai, Zuying
AU - Wu, Qihui
AU - Hu, Meiqin
AU - Wang, Yuan
AU - Huang, Rong
AU - Zhang, Xiaoyu
AU - Wu, Xi
AU - Sun, Lei
AU - Wang, Yeshi
AU - Wang, Li
AU - Xu, Huadong
AU - Teng, Sasa
AU - Liu, Bing
AU - Zheng, Lianghong
AU - Zhang, Chen
AU - Zhang, Fukang
AU - Feng, Xinghua
AU - Zhu, Desheng
AU - Wang, Changhe
AU - Liu, Tao
AU - Zhu, Michael X.
AU - Zhou, Zhuan
PY - 2016
Y1 - 2016
N2 - Transient receptor potential A1 (TRPA1) is a nonselective cation channel implicated in thermosensation and inflammatory pain. In this study, we show that TRPA1 (activated by allyl isothiocyanate, acrolein, and 4-hydroxynonenal) elevates the intracellular Ca2+ concentration ([Ca2+]i) in dorsal root ganglion (DRG) neurons in the presence and absence of extracellular Ca2+. Pharmacological and immunocytochemical analyses revealed the presence of TRPA1 channels both on the plasma membrane and in endolysosomes. Confocal line-scan imaging demonstrated Ca2+ signals elicited from individual endolysosomes ("lysosome Ca2+ sparks") by TRPA1 activation. In physiological solutions, the TRPA1- mediated endolysosomal Ca2+ release contributed to ~40% of the overall [Ca2+]i rise and directly triggered vesicle exocytosis and calcitonin gene-related peptide release, which greatly enhanced the excitability of DRG neurons. Thus, in addition to working via Ca2+ influx, TRPA1 channels trigger vesicle release in sensory neurons by releasing Ca2+ from lysosome-like organelles.
AB - Transient receptor potential A1 (TRPA1) is a nonselective cation channel implicated in thermosensation and inflammatory pain. In this study, we show that TRPA1 (activated by allyl isothiocyanate, acrolein, and 4-hydroxynonenal) elevates the intracellular Ca2+ concentration ([Ca2+]i) in dorsal root ganglion (DRG) neurons in the presence and absence of extracellular Ca2+. Pharmacological and immunocytochemical analyses revealed the presence of TRPA1 channels both on the plasma membrane and in endolysosomes. Confocal line-scan imaging demonstrated Ca2+ signals elicited from individual endolysosomes ("lysosome Ca2+ sparks") by TRPA1 activation. In physiological solutions, the TRPA1- mediated endolysosomal Ca2+ release contributed to ~40% of the overall [Ca2+]i rise and directly triggered vesicle exocytosis and calcitonin gene-related peptide release, which greatly enhanced the excitability of DRG neurons. Thus, in addition to working via Ca2+ influx, TRPA1 channels trigger vesicle release in sensory neurons by releasing Ca2+ from lysosome-like organelles.
UR - https://www.scopus.com/pages/publications/84995923553
U2 - 10.1083/jcb.201603081
DO - 10.1083/jcb.201603081
M3 - 文献综述
C2 - 27799370
AN - SCOPUS:84995923553
SN - 0021-9525
VL - 215
SP - 369
EP - 381
JO - Journal of Cell Biology
JF - Journal of Cell Biology
IS - 3
ER -