<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rodrigues-Amorim D</submitter><funding>Fundação para a Ciência e a Tecnologia</funding><funding>Instituto de Salud Carlos III</funding><funding>Axencia Galega de Innovación</funding><pagination>8499</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8395201</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(16)</volume><pubmed_abstract>The neurobiology of schizophrenia is multifactorial, comprising the dysregulation of several biochemical pathways and molecules. This research proposes a peripheral biomarker for schizophrenia that involves the second extracellular loop of norepinephrine transporter (NEText), the tropomyosin receptor kinase C (TrkC), and the neurotrophin-3 (NT-3) in T cells. The study of NEText, NT-3, and TrkC was performed in T cells and plasma extracted from peripheral blood of 54 patients with schizophrenia and 54 healthy controls. Levels of NT-3, TrkC, and NET were significantly lower in plasma and T cells of patients compared to healthy controls. Co-immunoprecipitation (co-IPs) showed protein interactions with Co-IP NEText-NT-3 and Co-IP NEText-TrkC. Computational modelling of protein-peptide docking </pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>The Role of the Second Extracellular Loop of Norepinephrine Transporter, Neurotrophin-3 and Tropomyosin Receptor Kinase C in T Cells: A Peripheral Biomarker in the Etiology of Schizophrenia.</pubmed_title><pmcid>PMC8395201</pmcid><funding_grant_id>P16/00405</funding_grant_id><funding_grant_id>SFRH/BD/135623/2018</funding_grant_id><funding_grant_id>IN607B 2018/17</funding_grant_id><funding_grant_id>PI20/00937</funding_grant_id><pubmed_authors>Garcia-Caballero A</pubmed_authors><pubmed_authors>Spuch C</pubmed_authors><pubmed_authors>Lopez-Garcia M</pubmed_authors><pubmed_authors>Rodrigues-Amorim D</pubmed_authors><pubmed_authors>Alvarez-Ariza M</pubmed_authors><pubmed_authors>Olivares JM</pubmed_authors><pubmed_authors>Freiria-Martinez L</pubmed_authors><pubmed_authors>Rodriguez-Jamardo C</pubmed_authors><pubmed_authors>Comis-Tuche M</pubmed_authors><pubmed_authors>de Las Heras E</pubmed_authors><pubmed_authors>Vallejo-Curto MDC</pubmed_authors><pubmed_authors>Fernandez-Palleiro P</pubmed_authors><pubmed_authors>Iglesias-Martinez-Almeida M</pubmed_authors><pubmed_authors>Rivera-Baltanas T</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Role of the Second Extracellular Loop of Norepinephrine Transporter, Neurotrophin-3 and Tropomyosin Receptor Kinase C in T Cells: A Peripheral Biomarker in the Etiology of Schizophrenia.</name><description>The neurobiology of schizophrenia is multifactorial, comprising the dysregulation of several biochemical pathways and molecules. This research proposes a peripheral biomarker for schizophrenia that involves the second extracellular loop of norepinephrine transporter (NEText), the tropomyosin receptor kinase C (TrkC), and the neurotrophin-3 (NT-3) in T cells. The study of NEText, NT-3, and TrkC was performed in T cells and plasma extracted from peripheral blood of 54 patients with schizophrenia and 54 healthy controls. Levels of NT-3, TrkC, and NET were significantly lower in plasma and T cells of patients compared to healthy controls. Co-immunoprecipitation (co-IPs) showed protein interactions with Co-IP NEText-NT-3 and Co-IP NEText-TrkC. Computational modelling of protein-peptide docking </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Aug</publication><modification>2026-04-08T07:46:31.426Z</modification><creation>2022-02-11T09:56:57.119Z</creation></dates><accession>S-EPMC8395201</accession><cross_references><pubmed>34445205</pubmed><doi>10.3390/ijms22168499</doi></cross_references></HashMap>