<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Spaethling JM</submitter><funding>NIMH NIH HHS</funding><funding>NIH Single Cell Analysis Program</funding><pagination>791-803</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5316103</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(3)</volume><pubmed_abstract>Investigation of human CNS disease and drug effects has been hampered by the lack of a system that enables single-cell analysis of live adult patient brain cells. We developed a culturing system, based on a papain-aided procedure, for resected adult human brain tissue removed during neurosurgery. We performed single-cell transcriptomics on over 300 cells, permitting identification of oligodendrocytes, microglia, neurons, endothelial cells, and astrocytes after 3 weeks in culture. Using deep sequencing, we detected over 12,000 expressed genes, including hundreds of cell-type-enriched mRNAs, lncRNAs and pri-miRNAs. We describe cell-type- and patient-specific transcriptional hierarchies. Single-cell transcriptomics on cultured live adult patient derived cells is a prime example of the promise</pubmed_abstract><journal>Cell reports</journal><pubmed_title>Primary Cell Culture of Live Neurosurgically Resected Aged Adult Human Brain Cells and Single Cell Transcriptomics.</pubmed_title><pmcid>PMC5316103</pmcid><funding_grant_id>R33 MH106637</funding_grant_id><funding_grant_id>U01 MH098953</funding_grant_id><funding_grant_id>MH106637</funding_grant_id><pubmed_authors>Sul JY</pubmed_authors><pubmed_authors>Grady MS</pubmed_authors><pubmed_authors>Spaethling JM</pubmed_authors><pubmed_authors>Lucas TH</pubmed_authors><pubmed_authors>Lee J</pubmed_authors><pubmed_authors>Chen HI</pubmed_authors><pubmed_authors>Dueck H</pubmed_authors><pubmed_authors>Na YJ</pubmed_authors><pubmed_authors>Bell TJ</pubmed_authors><pubmed_authors>Khaladkar M</pubmed_authors><pubmed_authors>Kim J</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Wolf JA</pubmed_authors><pubmed_authors>Fisher SA</pubmed_authors><pubmed_authors>Ulyanova AV</pubmed_authors><pubmed_authors>Kung DK</pubmed_authors><pubmed_authors>Baltuch GH</pubmed_authors><pubmed_authors>Garcia MP</pubmed_authors><pubmed_authors>O'Rourke DM</pubmed_authors><pubmed_authors>Bartfai T</pubmed_authors><pubmed_authors>Stefanik D</pubmed_authors><pubmed_authors>Eberwine JH</pubmed_authors><pubmed_authors>Brem S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Primary Cell Culture of Live Neurosurgically Resected Aged Adult Human Brain Cells and Single Cell Transcriptomics.</name><description>Investigation of human CNS disease and drug effects has been hampered by the lack of a system that enables single-cell analysis of live adult patient brain cells. We developed a culturing system, based on a papain-aided procedure, for resected adult human brain tissue removed during neurosurgery. We performed single-cell transcriptomics on over 300 cells, permitting identification of oligodendrocytes, microglia, neurons, endothelial cells, and astrocytes after 3 weeks in culture. Using deep sequencing, we detected over 12,000 expressed genes, including hundreds of cell-type-enriched mRNAs, lncRNAs and pri-miRNAs. We describe cell-type- and patient-specific transcriptional hierarchies. Single-cell transcriptomics on cultured live adult patient derived cells is a prime example of the promise</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Jan</publication><modification>2026-04-14T09:35:56.922Z</modification><creation>2019-03-27T02:36:50Z</creation></dates><accession>S-EPMC5316103</accession><cross_references><pubmed>28099855</pubmed><doi>10.1016/j.celrep.2016.12.066</doi></cross_references></HashMap>