PMID- 18171944 OWN - NLM STAT- MEDLINE DCOM- 20080207 LR - 20220316 IS - 1529-2401 (Electronic) IS - 0270-6474 (Print) IS - 0270-6474 (Linking) VI - 28 IP - 1 DP - 2008 Jan 2 TI - A transcriptome database for astrocytes, neurons, and oligodendrocytes: a new resource for understanding brain development and function. PG - 264-78 LID - 10.1523/JNEUROSCI.4178-07.2008 [doi] AB - Understanding the cell-cell interactions that control CNS development and function has long been limited by the lack of methods to cleanly separate neural cell types. Here we describe methods for the prospective isolation and purification of astrocytes, neurons, and oligodendrocytes from developing and mature mouse forebrain. We used FACS (fluorescent-activated cell sorting) to isolate astrocytes from transgenic mice that express enhanced green fluorescent protein (EGFP) under the control of an S100beta promoter. Using Affymetrix GeneChip Arrays, we then created a transcriptome database of the expression levels of >20,000 genes by gene profiling these three main CNS neural cell types at various postnatal ages between postnatal day 1 (P1) and P30. This database provides a detailed global characterization and comparison of the genes expressed by acutely isolated astrocytes, neurons, and oligodendrocytes. We found that Aldh1L1 is a highly specific antigenic marker for astrocytes with a substantially broader pattern of astrocyte expression than the traditional astrocyte marker GFAP. Astrocytes were enriched in specific metabolic and lipid synthetic pathways, as well as the draper/Megf10 and Mertk/integrin alpha(v)beta5 phagocytic pathways suggesting that astrocytes are professional phagocytes. Our findings call into question the concept of a "glial" cell class as the gene profiles of astrocytes and oligodendrocytes are as dissimilar to each other as they are to neurons. This transcriptome database of acutely isolated purified astrocytes, neurons, and oligodendrocytes provides a resource to the neuroscience community by providing improved cell-type-specific markers and for better understanding of neural development, function, and disease. FAU - Cahoy, John D AU - Cahoy JD AD - Department of Neurobiology, Stanford University School of Medicine, Stanford, California 94305, USA. jcahoy@stanford.edu FAU - Emery, Ben AU - Emery B FAU - Kaushal, Amit AU - Kaushal A FAU - Foo, Lynette C AU - Foo LC FAU - Zamanian, Jennifer L AU - Zamanian JL FAU - Christopherson, Karen S AU - Christopherson KS FAU - Xing, Yi AU - Xing Y FAU - Lubischer, Jane L AU - Lubischer JL FAU - Krieg, Paul A AU - Krieg PA FAU - Krupenko, Sergey A AU - Krupenko SA FAU - Thompson, Wesley J AU - Thompson WJ FAU - Barres, Ben A AU - Barres BA LA - eng GR - R01 NS045621/NS/NINDS NIH HHS/United States GR - R01 DK054388/DK/NIDDK NIH HHS/United States GR - F32 EY007033/EY/NEI NIH HHS/United States GR - R01 CA095030/CA/NCI NIH HHS/United States GR - R01 EY010257/EY/NEI NIH HHS/United States GR - T32 EY007033/EY/NEI NIH HHS/United States GR - CA095030/CA/NCI NIH HHS/United States GR - T32 GM007365/GM/NIGMS NIH HHS/United States GR - GM07365/GM/NIGMS NIH HHS/United States GR - DK54388/DK/NIDDK NIH HHS/United States GR - EY07033/EY/NEI NIH HHS/United States GR - R01 EY10257/EY/NEI NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't PL - United States TA - J Neurosci JT - The Journal of neuroscience : the official journal of the Society for Neuroscience JID - 8102140 RN - 147336-22-9 (Green Fluorescent Proteins) SB - IM MH - Animals MH - Astrocytes/*physiology MH - *Brain/cytology/growth & development/metabolism MH - *Gene Expression Profiling MH - Gene Expression Regulation, Developmental/physiology MH - Green Fluorescent Proteins/genetics/metabolism MH - Mice MH - Mice, Transgenic MH - Neurons/*physiology MH - Oligodendroglia/*physiology MH - Oligonucleotide Array Sequence Analysis/methods MH - *Transcription, Genetic PMC - PMC6671143 EDAT- 2008/01/04 09:00 MHDA- 2008/02/08 09:00 PMCR- 2008/07/02 CRDT- 2008/01/04 09:00 PHST- 2008/01/04 09:00 [pubmed] PHST- 2008/02/08 09:00 [medline] PHST- 2008/01/04 09:00 [entrez] PHST- 2008/07/02 00:00 [pmc-release] AID - 28/1/264 [pii] AID - 3301574 [pii] AID - 10.1523/JNEUROSCI.4178-07.2008 [doi] PST - ppublish SO - J Neurosci. 2008 Jan 2;28(1):264-78. doi: 10.1523/JNEUROSCI.4178-07.2008.