科研之友
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摘要
The adult zebrafish retina continuously produces rod photoreceptors from infrequent Muller glial cell division, yielding neuronal progenitor cells that migrate to the outer nuclear layer and become rod precursor cells that are committed to differentiate into rods. Retinal damage models suggested that rod cell death induces regeneration from rod precursor cells, whereas loss of any other retinal neurons activates Muller glia proliferation to produce pluripotent neuronal progenitors that can generate any other neuronal cell type in the retina. We tested this hypothesis by creating two transgenic lines that expressed the E. coli nitroreductase enzyme fused to EGFP (NTR-EGFP) in only rods. Treating transgenic adults with metronidazole resulted in two rod cell death models. First, killing all rods throughout the Tg(zop:nfsB-EGFP)(nt19) retina induced robust Muller glial proliferation, which yielded clusters of neuronal progenitor cells. In contrast, ablating only a subset of rods across the Tg(zop:nfsB-EGFP)(nt20) retina led to rod precursor, but not Muller glial, cell proliferation. We propose that two different criteria determine whether rod cell death will induce a regenerative response from the Muller glia rather than from the resident rod precursor cells in the ONL. First, there must be a large amount of rod cell death to initiate Muller glia proliferation. Second, the rod cell death must be acute, rather than chronic, to stimulate regeneration from the Muller glia. This suggests that the zebrafish retina possesses mechanisms to quantify the amount and timing of rod cell death. J. Comp. Neurol. 518: 800 - 814, 2010.
- 出版日期2010-3-15
