TRPM1 is a component of the retinal ON bipolar cell transduction channel in the mGluR6 cascade
Author(s) -
Chieko Koike,
Takehisa Obara,
Yoshitsugu Uriu,
Tomohiro Numata,
Rikako Sanuki,
Kentarou Miyata,
Toshiyuki Koyasu,
Shinji Ueno,
Kazuo Funabiki,
Akiko Tani,
Hiroshi Ueda,
Mineo Kondo,
Yasuo Mori,
Masao Tachibana,
Takahisa Furukawa
Publication year - 2009
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0912730107
Subject(s) - metabotropic glutamate receptor 6 , microbiology and biotechnology , metabotropic glutamate receptor , metabotropic glutamate receptor 1 , biology , transduction (biophysics) , metabotropic glutamate receptor 5 , glutamate receptor , chemistry , biochemistry , receptor
An essential step in intricate visual processing is the segregation of visual signals into ON and OFF pathways by retinal bipolar cells (BCs). Glutamate released from photoreceptors modulates the photoresponse of ON BCs via metabotropic glutamate receptor 6 (mGluR6) and G protein (Go) that regulates a cation channel. However, the cation channel has not yet been unequivocally identified. Here, we report a mouse TRPM1 long form (TRPM1-L) as the cation channel. We found that TRPM1-L localization is developmentally restricted to the dendritic tips of ON BCs in colocalization with mGluR6. TRPM1 null mutant mice completely lose the photoresponse of ON BCs but not that of OFF BCs. In the TRPM1-L-expressing cells, TRPM1-L functions as a constitutively active nonselective cation channel and its activity is negatively regulated by Go in the mGluR6 cascade. These results demonstrate that TRPM1-L is a component of the ON BC transduction channel downstream of mGluR6 in ON BCs.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom