PMID- 17640634 OWN - NLM STAT- MEDLINE DCOM- 20071109 LR - 20091119 IS - 0014-4835 (Print) IS - 0014-4835 (Linking) VI - 85 IP - 3 DP - 2007 Sep TI - Temporal and spatial differences in expression of TrkB isoforms in rat retina during constant light exposure. PG - 346-55 AB - Brain-derived neurotrophic factor (BDNF) has been reported to rescue neuroretinal cells under different toxic conditions. These cells include not only those expressing BDNF receptors (TrkB) but also those not expressing TrkB including photoreceptors. The purpose of this study was to determine the retinal sites at which BDNF and TrkB isoforms are expressed after different durations of continuous light exposure, and to compare these sites with those of TUNEL-positive cells in the same retina. Sprague-Dawley rats were exposed to continuous light for different durations. The expressions of BDNF and TrkB isoforms, TrkB-FL and TrkB-T1, were determined by Western blot analysis, real-time PCR, immunohistochemistry, and in situ hybridization before and after the light exposure. The number of TUNEL-positive cells reached a maximum at 48 to 72h after light exposure. The degree of up-regulation of the TrkB-T1 gene was significantly higher than that in normal control eyes at 24h by real-time PCR. Immunohistochemistry showed that TrkB-FL-positive cells were detected in all retinal layers except the outer nuclear layer (ONL), photoreceptor cells, and retinal pigment epithelium (RPE). The number of TrkB-FL-positive cells in the IPL was transiently decreased at 6h, and was increased on the processes of the Mueller cells in the ONL after 48h. TrkB-T1 was expressed in the INL, OPL, and RPE, and was up-regulated on the soma of Mueller cells after 24h. In situ hybridization showed that the expression of the TrkB-FL gene was up-regulated in the INL after 48h when the number of TUNEL-positive cells was at its peak. The TrkB-T1 gene was up-regulated before or just prior to the appearance of TUNEL-positive cells. These results suggest that BDNF transduces the signals using appropriate receptor isoforms that are expressed temporally and spatially differentially on Mueller cells during light-induced retinal degeneration. FAU - Asai, Nobuharu AU - Asai N AD - Division of Clinical Cell Therapy, Center for Translational and Advanced Animal Research, Tohoku University, Graduate School of Medicine, 1-1 Seiryoumachi, Aobaku, Sendai, Miyagi 980-8574, Japan. FAU - Abe, Toshiaki AU - Abe T FAU - Saito, Takae AU - Saito T FAU - Sato, Hajime AU - Sato H FAU - Ishiguro, Sei-Ichi AU - Ishiguro S FAU - Nishida, Kohji AU - Nishida K LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20070615 PL - England TA - Exp Eye Res JT - Experimental eye research JID - 0370707 RN - 0 (Brain-Derived Neurotrophic Factor) RN - 0 (Eye Proteins) RN - 0 (Protein Isoforms) RN - EC 2.7.10.1 (Receptor, trkB) SB - IM MH - Animals MH - Apoptosis/radiation effects MH - Brain-Derived Neurotrophic Factor/genetics/metabolism MH - Eye Proteins/genetics/*metabolism MH - Gene Expression Regulation/radiation effects MH - Immunoenzyme Techniques MH - *Light MH - Male MH - Photic Stimulation/methods MH - Photoreceptor Cells, Vertebrate/radiation effects MH - Protein Isoforms/genetics/metabolism MH - Rats MH - Rats, Sprague-Dawley MH - Receptor, trkB/genetics/*metabolism MH - Retina/*metabolism/*radiation effects MH - Reverse Transcriptase Polymerase Chain Reaction/methods EDAT- 2007/07/21 09:00 MHDA- 2007/11/10 09:00 CRDT- 2007/07/21 09:00 PHST- 2007/02/08 00:00 [received] PHST- 2007/05/12 00:00 [revised] PHST- 2007/05/30 00:00 [accepted] PHST- 2007/07/21 09:00 [pubmed] PHST- 2007/11/10 09:00 [medline] PHST- 2007/07/21 09:00 [entrez] AID - S0014-4835(07)00157-1 [pii] AID - 10.1016/j.exer.2007.05.010 [doi] PST - ppublish SO - Exp Eye Res. 2007 Sep;85(3):346-55. doi: 10.1016/j.exer.2007.05.010. Epub 2007 Jun 15.