The Ventral Tegmental Area has calbindin neurons with the capability to co-release glutamate and dopamine into the nucleus accumbens.
Animals
Calbindins
/ metabolism
Dopamine
/ metabolism
Dopaminergic Neurons
/ metabolism
GABAergic Neurons
/ metabolism
Glutamic Acid
/ metabolism
Nucleus Accumbens
/ metabolism
Rats
Tyrosine 3-Monooxygenase
/ metabolism
Ventral Tegmental Area
/ metabolism
Vesicular Inhibitory Amino Acid Transport Proteins
/ metabolism
VGluT2
VTA
calbindin
calretinin
parvalbumin
Journal
The European journal of neuroscience
ISSN: 1460-9568
Titre abrégé: Eur J Neurosci
Pays: France
ID NLM: 8918110
Informations de publication
Date de publication:
12 2019
12 2019
Historique:
received:
05
12
2018
revised:
21
05
2019
accepted:
10
06
2019
pubmed:
20
6
2019
medline:
24
9
2020
entrez:
20
6
2019
Statut:
ppublish
Résumé
The ventral tegmental area (VTA) has three major classes of neurons: dopaminergic (expressing tyrosine hydroxylase; TH), GABAergic (expressing vesicular GABA transporter; VGaT) and glutamatergic (expressing vesicular glutamate transporter 2; VGluT2). While VTA dopaminergic and GABAergic neurons have been further characterized by expression of calcium-binding proteins (calbindin, CB; calretinin, CR or parvalbumin, PV), it is unclear whether these proteins are expressed in rat VTA glutamatergic neurons. Here, by a combination of in situ hybridization (for VGluT2 mRNA detection) and immunohistochemistry (for CB-, CR- or PV-detection), we found that among the total population of VGluT2 neurons, 30% coexpressed CB, 3% coexpressed PV and <1% coexpressed CR. Given that some VGluT2 neurons coexpress TH or VGaT, we examined whether these neurons coexpress CB, and found that about 20% of VGluT2-CB neurons coexpressed TH and about 13% coexpressed VGaT. Because VTA TH-CB neurons are known to target the nucleus accumbens (nAcc), we determined whether VGluT2-CB-TH neurons innervate nAcc, and found that about 80% of VGluT2-CB neurons innervating the nAcc shell coexpressed TH. In summary, (a) CB, PV and CR are detected in subpopulations of VTA-VGluT2 neurons; (b) CB is the main calcium-binding protein present in VTA-VGluT2 neurons; (c) one-third of VTA-VGluT2 neurons coexpress CB; (d) some VTA-VGluT2-CB neurons have the capability to co-release dopamine or GABA, and (e) a subpopulation of VTA glutamatergic-dopaminergic neurons innervates nAcc shell. These findings further provide evidence for molecular diversity among VTA-VGluT2 neurons, neurons that may play a role in specific circuitry and behaviours.
Identifiants
pubmed: 31215698
doi: 10.1111/ejn.14493
pmc: PMC6920608
mid: NIHMS1036454
doi:
Substances chimiques
Calbindins
0
Vesicular Inhibitory Amino Acid Transport Proteins
0
vesicular GABA transporter
0
Glutamic Acid
3KX376GY7L
Tyrosine 3-Monooxygenase
EC 1.14.16.2
Dopamine
VTD58H1Z2X
Types de publication
Journal Article
Research Support, N.I.H., Intramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
3968-3984Subventions
Organisme : Intramural NIH HHS
ID : ZIA DA000511-12
Pays : United States
Informations de copyright
Published 2019. This article is a U.S. Government work and is in the public domain in the USA.
Références
Synapse. 2007 Feb;61(2):87-95
pubmed: 17117419
J Neurosci. 2015 Dec 2;35(48):15948-54
pubmed: 26631475
Brain Struct Funct. 2013 Sep;218(5):1159-76
pubmed: 22926514
Neuron. 2017 Apr 5;94(1):138-152.e5
pubmed: 28384468
J Neurosci. 2002 Aug 1;22(15):6732-41
pubmed: 12151552
Brain Res. 1987 Jul 28;416(2):369-74
pubmed: 3304536
J Neurosci. 2014 Oct 15;34(42):13906-10
pubmed: 25319687
Hum Mol Genet. 2005 Jul 1;14(13):1709-25
pubmed: 15888489
J Comp Neurol. 2006 Oct 10;498(5):581-92
pubmed: 16917821
Neurobiol Dis. 2005 Feb;18(1):19-31
pubmed: 15649693
Exp Brain Res. 1994;99(1):34-42
pubmed: 7925794
Cell Rep. 2018 Jun 19;23(12):3465-3479
pubmed: 29924991
J Comp Neurol. 2008 Jul 20;509(3):302-18
pubmed: 18478589
Cell. 2018 Aug 9;174(4):1015-1030.e16
pubmed: 30096299
Neuroscience. 2014 Dec 12;282:198-216
pubmed: 25241061
J Neurosci. 2002 Feb 15;22(4):1290-302
pubmed: 11850457
J Comp Neurol. 2014 Oct 1;522(14):3308-34
pubmed: 24715505
Neurosci Lett. 1987 Jun 26;77(3):255-60
pubmed: 3302765
Nat Neurosci. 2016 May;19(5):725-733
pubmed: 27019014
Nat Neurosci. 2012 Jun;15(6):813-5
pubmed: 22544312
Eur J Neurosci. 2007 Jan;25(1):106-18
pubmed: 17241272
Science. 1986 Feb 28;231(4741):995-7
pubmed: 3945815
Front Behav Neurosci. 2018 Jul 18;12:146
pubmed: 30072881
Neurosci Lett. 1989 Apr 24;99(1-2):6-11
pubmed: 2748019
Nature. 1981 Sep 24;293(5830):300-2
pubmed: 7278987
Nat Rev Neurosci. 2017 Feb;18(2):73-85
pubmed: 28053327
Nat Neurosci. 2014 Nov;17(11):1543-51
pubmed: 25242304
J Comp Neurol. 1990 Mar 22;293(4):599-615
pubmed: 2329196
iScience. 2018 Apr 27;2:51-62
pubmed: 29888759
Brain Res. 1999 Oct 30;846(1):129-36
pubmed: 10536220
Brain Res. 1999 Oct 9;844(1-2):67-77
pubmed: 10536262
J Neurosci. 2010 Jan 6;30(1):218-29
pubmed: 20053904
Brain Res. 1992 Aug 7;587(2):203-10
pubmed: 1356063
Nat Commun. 2016 Dec 15;7:13697
pubmed: 27976722
J Neurosci. 2010 Jun 16;30(24):8229-33
pubmed: 20554874
Eur J Neurosci. 2011 Dec;34(12):1934-43
pubmed: 22128821
Exp Brain Res. 1989;76(2):467-72
pubmed: 2767197
J Comp Neurol. 1990 Aug 1;298(1):1-22
pubmed: 2170466
PLoS One. 2018 Jun 12;13(6):e0198991
pubmed: 29894514
Eur J Neurosci. 2000 Dec;12(12):4578-82
pubmed: 11122372
Nat Neurosci. 2015 Mar;18(3):386-92
pubmed: 25664911
Proc Natl Acad Sci U S A. 1989 Mar;86(6):2093-7
pubmed: 2648389
J Comp Neurol. 1988 Feb 1;268(1):29-37
pubmed: 3346382
J Comp Neurol. 1983 Aug 1;218(2):220-38
pubmed: 6886073
Nat Neurosci. 2018 Sep;21(9):1260-1271
pubmed: 30104732
J Comp Neurol. 1990 Nov 15;301(3):417-32
pubmed: 2262599
Exp Brain Res. 1987;66(1):191-210
pubmed: 2884126
J Comp Neurol. 1992 Jun 15;320(3):353-69
pubmed: 1613130
PLoS One. 2012;7(7):e42365
pubmed: 22860119
J Neurosci. 2010 May 19;30(20):7105-10
pubmed: 20484653
Neuroscience. 1996 Nov;75(2):523-33
pubmed: 8931015
J Neurosci. 2011 Jun 8;31(23):8476-90
pubmed: 21653852