Bipolar cells of the mouse retina: a gene gun, morphological study.
Bipolar cells of the mouse retina: a gene gun, morphological study.
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小鼠视网膜双极细胞:基因枪,形态学研究。
DOI:
10.1002/cne.20207
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发表时间:
2004
期刊:
影响因子:
--
通讯作者:
Strettoi,Enrica
中科院分区:
文献类型:
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作者:
Pignatelli,Vincenzo;Strettoi,Enrica
One of the key elements concerning our understanding of the organization of the mouse retina is the complete classification of the various types of bipolar cells. With the present study, we tried to contribute to this important issue. Unfortunately, most of the antibodies that stain specifically bipolar cells in the retina of other mammals hardly work for the retina of the mouse. We succeeded in overcoming this limitation by using a relatively novel technique based on the gene gun transfer of fluorescent dyes to cells. Hence, we were able to stain a considerable number of bipolar cells that could be characterized according to morphological and comparative criteria. We also performed a complete morphometric analysis of a subset of bipolar cells stained by anti–neurokinin-3 receptor antibodies. We found nine types of cone bipolar cells and one type of rod bipolar cell; these data are consistent with the findings of previous studies on the retinas of other mammals, such as rabbits, rats, and monkeys and with a recent study based on the mouse retina (Ghosh et al.[2004] J Comp Neurol 469: 70–82). Our results also confirm the existence of a common structural similarity among mammalian retinas. It remains to be elucidated what is exactly the functional role of the various types of cone bipolar cells and what is the specific contribution they provide to the perception of a given visual stimulus. Most probably, each bipolar cell type constitutes a specialized channel for the computation of a selected component of the visual stimulus. More complex signal coding, involving the coordinated activity of various types of bipolar cells, could also be postulated, as it has been shown for ganglion cells (Meister [1996] Proc Natl Acad Sci USA 93: 609–614). J. Comp. Neurol. 476: 254–266, 2004.© 2004 Wiley-Liss, Inc.