Deep Survey of GABAergic Interneurons: Emerging Insights From Gene-Isoform Transcriptomics.
GABAergic interneuron
cell type classification
gene isoforms
single-cell RNA seq
trans-synaptic signaling
Journal
Frontiers in molecular neuroscience
ISSN: 1662-5099
Titre abrégé: Front Mol Neurosci
Pays: Switzerland
ID NLM: 101477914
Informations de publication
Date de publication:
2019
2019
Historique:
received:
08
03
2019
accepted:
23
04
2019
entrez:
29
5
2019
pubmed:
28
5
2019
medline:
28
5
2019
Statut:
epublish
Résumé
GABAergic interneuron diversity is a key feature in the brain that helps to create different brain activity patterns and behavioral states. Cell type classification schemes-based on anatomical, physiological and molecular features-have provided us with a detailed understanding of the distinct types that constitute this diversity and their contribution to brain function. Over recent years, the utility of single-cell RNAseq has majorly complemented this existing framework, vastly expanding our knowledge base, particularly regarding molecular features. Single-cell gene-expression profiles of tens of thousands of GABAergic cells from many different types are now available. The analysis of these data has shed new lights onto previous classification principles and illuminates a path towards a deeper understanding of molecular hallmarks behind interneuron diversity. A large part of such molecular features is synapse-related. These include ion channels and receptors, as well as key synaptic organizers and trans-synaptic signaling molecules. Increasing evidence suggests that transcriptional and post-transcriptional modifications further diversify these molecules and generate cell type-specific features. Thus, unraveling the cell type-specific nature of gene-isoform expression will be a key in cell type classification. This review article discusses progress in the transcriptomic survey of interneurons and insights that have begun to manifest from isoform-level analyses.
Identifiants
pubmed: 31133800
doi: 10.3389/fnmol.2019.00115
pmc: PMC6514532
doi:
Types de publication
Journal Article
Langues
eng
Pagination
115Références
Neuron. 1992 Jun;8(6):1161-70
pubmed: 1319186
J Neurosci. 2004 Jun 23;24(25):5816-26
pubmed: 15215304
J Physiol. 2005 Jan 1;562(Pt 1):73-80
pubmed: 15498801
Science. 1990 Sep 28;249(4976):1580-5
pubmed: 1699275
J Biol Chem. 2006 Nov 17;281(46):34918-25
pubmed: 17001074
Neuron. 2007 Oct 4;56(1):33-42
pubmed: 17920013
Nat Rev Neurosci. 2008 Jul;9(7):557-68
pubmed: 18568015
Science. 2008 Jul 4;321(5885):53-7
pubmed: 18599766
J Neurosci. 2009 May 27;29(21):7040-52
pubmed: 19474331
Neuron. 2009 Sep 10;63(5):628-42
pubmed: 19755106
Nature. 2010 May 6;465(7294):53-9
pubmed: 20445623
Dev Neurobiol. 2011 Jan 1;71(1):45-61
pubmed: 21154909
J Neurosci. 2011 Jul 27;31(30):10948-70
pubmed: 21795545
J Cell Sci. 2011 Aug 15;124(Pt 16):2786-96
pubmed: 21807943
Cell. 2011 Sep 30;147(1):132-46
pubmed: 21924763
Nature. 2012 Aug 23;488(7412):517-21
pubmed: 22842903
Neuron. 2013 May 8;78(3):498-509
pubmed: 23583622
Cell. 2013 Jul 3;154(1):75-88
pubmed: 23827676
Trends Neurosci. 2013 Sep;36(9):522-34
pubmed: 23835198
Nature. 2014 Jan 16;505(7483):318-26
pubmed: 24429630
J Cell Biol. 2014 Feb 3;204(3):331-42
pubmed: 24469635
Proc Natl Acad Sci U S A. 2014 Apr 1;111(13):E1291-9
pubmed: 24639501
Front Cell Neurosci. 2014 Apr 09;8:103
pubmed: 24782709
Neuron. 2014 Oct 22;84(2):386-98
pubmed: 25284007
Nat Rev Genet. 2015 Mar;16(3):133-45
pubmed: 25628217
Science. 2015 Mar 6;347(6226):1138-42
pubmed: 25700174
Elife. 2015 May 18;4:e07794
pubmed: 25985086
Neuron. 2015 Jul 15;87(2):326-40
pubmed: 26182417
Nat Rev Neurosci. 2016 Jan;17(1):22-35
pubmed: 26656254
Nat Biotechnol. 2016 Feb;34(2):199-203
pubmed: 26689543
Nat Biotechnol. 2016 Feb;34(2):175-183
pubmed: 26689544
Nat Neurosci. 2016 Feb;19(2):335-46
pubmed: 26727548
Science. 2016 May 20;352(6288):982-6
pubmed: 27174676
Proc Natl Acad Sci U S A. 2016 Aug 30;113(35):E5222-31
pubmed: 27531958
Cell. 2016 Aug 25;166(5):1147-1162.e15
pubmed: 27565344
Nat Neurosci. 2016 Aug 26;19(9):1131-41
pubmed: 27571192
Elife. 2016 Dec 13;5:
pubmed: 27960072
BMC Genomics. 2017 Feb 3;18(1):126
pubmed: 28158971
Nat Rev Neurosci. 2017 May;18(5):299-309
pubmed: 28381833
Science. 2017 Apr 28;356(6336):406-411
pubmed: 28450636
Science. 2017 Apr 28;356(6336):411-414
pubmed: 28450637
Neuron. 2017 May 3;94(3):611-625.e4
pubmed: 28472659
Curr Opin Neurobiol. 2017 Aug;45:162-168
pubmed: 28609697
Cell. 2017 Oct 19;171(3):522-539.e20
pubmed: 28942923
Physiol Rev. 2017 Oct 1;97(4):1619-1747
pubmed: 28954853
PLoS Genet. 2017 Oct 25;13(10):e1007073
pubmed: 29069083
Cell. 2017 Nov 2;171(4):745-769
pubmed: 29100073
Neuron. 2017 Nov 15;96(4):808-826.e8
pubmed: 29107521
Cell. 2017 Nov 16;171(5):1206-1220.e22
pubmed: 29149607
Science. 2018 Apr 6;360(6384):81-85
pubmed: 29472441
Nature. 2018 Mar 22;555(7697):457-462
pubmed: 29513653
Nature. 2018 Mar 22;555(7697):524-528
pubmed: 29539641
Science. 2018 Apr 13;360(6385):176-182
pubmed: 29545511
PLoS Biol. 2018 Jun 18;16(6):e2006387
pubmed: 29912866
Cell Tissue Res. 2018 Sep;373(3):619-641
pubmed: 30084021
Nature. 2018 Aug;560(7719):494-498
pubmed: 30089906
Genome Biol. 2018 Aug 15;19(1):117
pubmed: 30111345
Cell Rep. 2018 Aug 21;24(8):2179-2190.e7
pubmed: 30134177
Nat Neurosci. 2018 Sep;21(9):1185-1195
pubmed: 30150662
Neuron. 2018 Nov 21;100(4):846-859.e7
pubmed: 30318414
Nat Biotechnol. 2018 Oct 15;:null
pubmed: 30320766
Neuron. 2018 Oct 24;100(2):294-313
pubmed: 30359598
Nature. 2018 Nov;563(7729):72-78
pubmed: 30382198
Science. 2018 Dec 14;362(6420):
pubmed: 30545856
Eur J Neurosci. 2018 Dec 27;:null
pubmed: 30589479
Science. 2019 Jan 25;363(6425):413-417
pubmed: 30679375
Neuron. 1995 Jul;15(1):193-204
pubmed: 7619522
Science. 1994 Dec 9;266(5191):1709-13
pubmed: 7992055
Hippocampus. 1996;6(4):347-470
pubmed: 8915675