PMID- 12111828 OWN - NLM STAT- MEDLINE DCOM- 20020814 LR - 20161124 IS - 0360-4012 (Print) IS - 0360-4012 (Linking) VI - 68 IP - 6 DP - 2002 Jun 15 TI - Comparative expression profiles of Trk receptors and Shc-related phosphotyrosine adapters during retinal development: potential roles of N-Shc/ShcC in brain-derived neurotrophic factor signal transduction and modulation. PG - 668-80 AB - Neurotrophins (NTs) have multiple roles in retinal development and survival, which are mediated through their specific receptors and signaling molecules. An emerging family of adapter protein, Shc (Src homology and collagen)-related molecules, i.e., Shc/ShcA, Sck/ShcB, and N-Shc/ShcC, has been implicated in various phosphotyrosine signal transduction mechanisms, including that for NTs. To explore the potential role(s) of Shc-related adapters in NT signaling in the retina, we compared the developmental changes of the mRNA expression of TrkA -B, and -C in the rat retina, on one hand and, on the other hand, studied which members of the Shc family were activated after brain-derived neurotrophic factor (BDNF) application in axotomized rat retinas. Early in development, both TrkA and ShcA were highly expressed, whereas, in late development to adulthood, TrkB/C and ShcB/C were highly expressed. In the mature retinal ganglion cell layer, the expression of ShcB/C and TrkB/C was evident. Immunoreactivity of ShcC was located in the retinal ganglion cells, amacrine cells, and inner plexiform layer. The response of ShcC following retinal axotomy was most profound with the administration of BDNF, and there was some response with neurotrophin-3. These results indicate that ShcC could be a potential phosphotyrosine adapter among the Shc family members for BDNF signaling and function during retinal development and regeneration in vivo. CI - Copyright 2002 Wiley-Liss, Inc. FAU - Nakazawa, Toru AU - Nakazawa T AD - Department of Molecular Genetics, National Institute for Longevity Sciences, Aichi, Japan. FAU - Nakano, Itsuko AU - Nakano I FAU - Sato, Masahiro AU - Sato M FAU - Nakamura, Takeshi AU - Nakamura T FAU - Tamai, Makoto AU - Tamai M FAU - Mori, Nozomu AU - Mori N LA - eng PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - J Neurosci Res JT - Journal of neuroscience research JID - 7600111 RN - 0 (Adaptor Proteins, Signal Transducing) RN - 0 (Brain-Derived Neurotrophic Factor) RN - 0 (Nerve Tissue Proteins) RN - 0 (Neuropeptides) RN - 0 (Proteins) RN - 0 (RNA, Messenger) RN - 0 (Receptors, Nerve Growth Factor) RN - 0 (SHC3 protein, human) RN - 0 (Shc Signaling Adaptor Proteins) RN - 0 (Shc1 protein, rat) RN - 0 (Shc2 protein, rat) RN - 0 (Shc3 protein, rat) RN - 0 (Src Homology 2 Domain-Containing, Transforming Protein 1) RN - 0 (Src Homology 2 Domain-Containing, Transforming Protein 2) RN - 0 (Src Homology 2 Domain-Containing, Transforming Protein 3) RN - 21820-51-9 (Phosphotyrosine) RN - EC 2.7.10.1 (Receptor, trkA) RN - EC 2.7.10.1 (Receptor, trkB) RN - EC 2.7.10.1 (Receptor, trkC) SB - IM MH - *Adaptor Proteins, Signal Transducing MH - Animals MH - Axotomy MH - Blotting, Western MH - Brain-Derived Neurotrophic Factor/metabolism/*pharmacology MH - Gene Expression Regulation MH - Immunohistochemistry MH - In Situ Hybridization MH - Male MH - Nerve Tissue Proteins/*analysis/drug effects/genetics MH - Neuropeptides/*metabolism MH - Phosphotyrosine/*metabolism MH - Plasmids MH - Precipitin Tests MH - Proteins/*analysis/drug effects/genetics MH - RNA, Messenger/analysis MH - Rats MH - Rats, Sprague-Dawley MH - Rats, Wistar MH - Receptor, trkA/*analysis/genetics MH - Receptor, trkB/*analysis/genetics MH - Receptor, trkC/*analysis/genetics MH - Receptors, Nerve Growth Factor/metabolism MH - Retina/*growth & development/metabolism MH - Reverse Transcriptase Polymerase Chain Reaction MH - Shc Signaling Adaptor Proteins MH - Signal Transduction MH - Src Homology 2 Domain-Containing, Transforming Protein 1 MH - Src Homology 2 Domain-Containing, Transforming Protein 2 MH - Src Homology 2 Domain-Containing, Transforming Protein 3 EDAT- 2002/07/12 10:00 MHDA- 2002/08/15 10:01 CRDT- 2002/07/12 10:00 PHST- 2002/07/12 10:00 [pubmed] PHST- 2002/08/15 10:01 [medline] PHST- 2002/07/12 10:00 [entrez] AID - 10.1002/jnr.10259 [doi] PST - ppublish SO - J Neurosci Res. 2002 Jun 15;68(6):668-80. doi: 10.1002/jnr.10259.