<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Majumdar S</submitter><funding>NEI NIH HHS</funding><funding>National Institute of Health</funding><pagination>1024</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12468242</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(9)</volume><pubmed_abstract>&lt;b>Background/Objectives&lt;/b>: Glutamatergic neurotransmission is essential for the normal functioning of the retina. Photoreceptor to bipolar and bipolar to ganglion cell signaling is mediated by L-glutamate, which is stored in and released from vesicular glutamate transporter 1 (VGLUT1) containing synaptic vesicles. VGLUT1 is expressed postnatally, P2 onwards, and is required for the glutamatergic retinal wave observed between P10 and P12 in the developing mouse retina. P9-P13 postnatal age is critical for retinal development as VGLUT1 expressing ribbon synapses activate in the outer and inner plexiform layers, and rod/cone mediated visual signaling commences in that period. Although it has been hypothesized that glutamatergic extrinsic signaling drives cell cycle exit and initiates cellu</pubmed_abstract><journal>Brain sciences</journal><pubmed_title>Genetic Loss of VGLUT1 Alters Histogenesis of Retinal Glutamatergic Cells and Reveals Dynamic Expression of VGLUT2 in Cones.</pubmed_title><pmcid>PMC12468242</pmcid><funding_grant_id>R37 EY001869</funding_grant_id><funding_grant_id>P30 EY002162</funding_grant_id><funding_grant_id>EY01869 and EY002162</funding_grant_id><funding_grant_id>R01 EY001869</funding_grant_id><pubmed_authors>Majumdar S</pubmed_authors><pubmed_authors>Wu V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genetic Loss of VGLUT1 Alters Histogenesis of Retinal Glutamatergic Cells and Reveals Dynamic Expression of VGLUT2 in Cones.</name><description>&lt;b>Background/Objectives&lt;/b>: Glutamatergic neurotransmission is essential for the normal functioning of the retina. Photoreceptor to bipolar and bipolar to ganglion cell signaling is mediated by L-glutamate, which is stored in and released from vesicular glutamate transporter 1 (VGLUT1) containing synaptic vesicles. VGLUT1 is expressed postnatally, P2 onwards, and is required for the glutamatergic retinal wave observed between P10 and P12 in the developing mouse retina. P9-P13 postnatal age is critical for retinal development as VGLUT1 expressing ribbon synapses activate in the outer and inner plexiform layers, and rod/cone mediated visual signaling commences in that period. Although it has been hypothesized that glutamatergic extrinsic signaling drives cell cycle exit and initiates cellu</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-05-02T03:11:10.305Z</modification><creation>2026-05-02T03:08:03.239Z</creation></dates><accession>S-EPMC12468242</accession><cross_references><pubmed>41008384</pubmed><doi>10.3390/brainsci15091024</doi></cross_references></HashMap>