Literature DB >> 25521284

Cone bipolar cells in the retina of the microbat Carollia perspicillata.

Elisabeth Butz1, Leo Peichl, Brigitte Müller.   

Abstract

We studied the retinal cone bipolar cells of Carollia perspicillata, a microchiropteran bat of the phyllostomid family. Microchiroptera are strongly nocturnal, with small eyes and rod-dominated retinae. However, they also possess a significant cone population (2-4%) comprising two spectral types, which are hence the basis for daylight and color vision. We used antibodies against the calcium-binding protein recoverin and the carbohydrate epitope 15 (CD15) as reliable markers for certain cone bipolar cells. Dye injections of recoverin- or CD15-prelabeled cone bipolar cells in vertical slices revealed the morphology of the axon terminal system of individual bipolar cells. Seven distinct cone bipolar cell types were identified. They differed in the morphology and stratification level of their axon terminal system in the inner plexiform layer and in immunoreactivity for recoverin and/or CD15. Additional immunocytochemical markers were used to assess the functional ON/OFF subdivision of the inner plexiform layer. In line with the extended thickness of the ON sublayer of the inner plexiform layer in the microbat retina, more ON than OFF cone bipolar cell types were found, namely, four versus three. Most likely, in the bats' predominantly dark environment, ON signals have greater importance for contrast perception. We conclude that the microbat retina conforms to the general mammalian blueprint, in which light signals of intensities above rod sensitivity are detected by cones and transmitted to various types of ON and OFF cone bipolar cells.
© 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  RRID:AB_152707; RRID:AB_2039906; RRID:AB_2086768; RRID:AB_2253622; RRID:AB_2301751; RRID:AB_2314432; RRID:AB_397181; RRID:AB_477345; bat vision; cone pathway; microchiroptera; photopic vision; retinal anatomy

Mesh:

Substances:

Year:  2015        PMID: 25521284     DOI: 10.1002/cne.23726

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


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