4.8 Article

TRPM1 is a component of the retinal ON bipolar cell transduction channel in the mGluR6 cascade

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.0912730107

Keywords

G protein; retina; photoresponse; glutamate; vision

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan
  2. Japan Science and Technology Agency
  3. Takeda Science Foundation
  4. Uehara Memorial Foundation
  5. Mochida Memorial Foundation
  6. Grants-in-Aid for Scientific Research [22790208, 20249015] Funding Source: KAKEN

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available