Volume sensing in the transient receptor potential vanilloid 4 ion channel is cell type?specific and mediated by an N-terminal volume-sensing domain

被引:24
|
作者
Toft-Bertelsen, Trine L. [1 ]
Yarishkin, Oleg [2 ]
Redmon, Sarah [2 ]
Phuong, Tam T. T. [2 ]
Krizaj, David [2 ]
MacAulay, Nanna [1 ]
机构
[1] Univ Copenhagen, Dept Neurosci, Blegdamsvej 3,Bldg 24-6, DK-2200 Copenhagen N, Denmark
[2] Univ Utah, Sch Med, Dept Ophthalmol & Visual Sci, Salt Lake City, UT 84132 USA
基金
美国国家卫生研究院;
关键词
transient receptor potential channels (TRP channels); aquaporin 4 (AQP4); polyunsaturated fatty acid (PUFA); lipid; retina; osmo-sensing; osmo-sensor; transient receptor potential vanilloid 4 (TRPV4); volume sensing; volume sensor; cell swelling; phospholipase A2 (PLA2); 5; 6?-epoxy-8Z; 11Z; 14Z-eicosatrienoic acid (5; 6?-EET); glaucoma; Xenopus oocytes; M?ller cells; retinal ganglion cells; CALCIUM HOMEOSTASIS; PHOSPHOLIPASE A(2); TRPV4; CHANNELS; ACTIVATION; VARIANT; NEURONS; MODULATION; SENSATION; PRESSURE; IDENTITY;
D O I
10.1074/jbc.RA119.011187
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
Many retinal diseases are associated with pathological cell swelling, but the underlying etiology remains to be established. A key component of the volume-sensitive machinery, the transient receptor potential vanilloid 4 (TRPV4) ion channel, may represent a sensor and transducer of cell swelling, but the molecular link between the swelling and TRPV4 activation is unresolved. Here, our results from experiments using electrophysiology, cell volumetric measurements, and fluorescence imaging conducted in murine retinal cells and Xenopus oocytes indicated that cell swelling in the physiological range activated TRPV4 in M?ller glia and Xenopus oocytes, but required phospholipase A(2) (PLA(2)) activity exclusively in M?ller cells. Volume-dependent TRPV4 gating was independent of cytoskeletal rearrangements and phosphorylation. Our findings also revealed that TRPV4-mediated transduction of volume changes is dependent by its N terminus, more specifically by its distal-most part. We conclude that the volume sensitivity and function of TRPV4 in situ depend critically on its functional and cell type?specific interactions.
引用
收藏
页码:18421 / 18434
页数:14
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