4.7 Article

Melanopsin-Positive Intrinsically Photosensitive Retinal Ganglion Cells: From Form to Function

期刊

JOURNAL OF NEUROSCIENCE
卷 31, 期 45, 页码 16094-16101

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.4132-11.2011

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资金

  1. NIH [EY06678, EY09625, EY014596, GM076430, EY012949, EY018885]
  2. National Research Service Award fellowship
  3. Visual Neuroscience Training Program training grant
  4. Champalimaud Foundation
  5. David and Lucille Packard Foundation
  6. Alfred P. Sloan Foundation
  7. Wellcome Trust
  8. Biotechnology and Biological Sciences Research Council
  9. European Research Council
  10. University of Minnesota
  11. Stein/Oppenheimer Endowment Award
  12. Harold and Pauline Price Chair in Ophthalmology
  13. Jules Stein Eye Institute
  14. BBSRC [BB/I007296/1] Funding Source: UKRI
  15. Biotechnology and Biological Sciences Research Council [BB/I007296/1] Funding Source: researchfish

向作者/读者索取更多资源

Melanopsin imparts an intrinsic photosensitivity to a subclass of retinal ganglion cells (ipRGCs). Generally thought of as irradiance detectors, ipRGCs target numerous brain regions involved in non-image-forming vision. ipRGCs integrate their intrinsic, melanopsin-mediated light information with rod/cone signals relayed via synaptic connections to influence light-dependent behaviors. Early observations indicated diversity among these cells and recently several specific subtypes have been identified. These subtypes differ in morphological and physiological form, controlling separate functions that range from biological rhythm via circadian photoentrainment, to protective behavioral responses including pupil constriction and light avoidance, and even image-forming vision. In this Mini-Symposium review, we will discuss some recent findings that highlight the diversity in both form and function of these recently discovered atypical photoreceptors.

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