L. Alberi, A. Lintas, R. Kretz, B. Schwaller, and A. E. Villa, The calcium-binding protein parvalbumin modulates the firing 1 properties of the reticular thalamic nucleus bursting neurons, J Neurophysiol, vol.109, pp.2827-2841, 2013.

C. M. Anderson and R. A. Swanson, Astrocyte glutamate transport: review of properties, regulation, and physiological functions, Glia, vol.32, pp.1-14, 2000.

K. Apazoglou, S. Farley, and V. Gorgievski, Antidepressive effects of targeting ELK-1 signal transduction, Nat Med, vol.24, pp.591-597, 2018.
URL : https://hal.archives-ouvertes.fr/hal-01909771

D. M. Armstrong, C. B. Saper, A. I. Levey, B. H. Wainer, and R. D. Terry, Distribution of cholinergic neurons in rat brain: demonstrated by the immunocytochemical localization of choline acetyltransferase, J Comp Neurol, vol.216, pp.53-68, 1983.

Y. Bernardinelli, I. Nikonenko, and D. Muller, Structural plasticity: mechanisms and contribution to developmental psychiatric disorders, Front Neuroanat, vol.8, p.123, 2014.

P. K. Blakely, S. Hussain, L. E. Carlin, and D. N. Irani, Astrocyte matricellular proteins that control excitatory synaptogenesis are regulated by inflammatory cytokines and correlate with paralysis severity during experimental autoimmune encephalomyelitis, Front Neurosci, vol.9, 2015.

P. Bornstein, Diversity of function is inherent in matricellular proteins: an appraisal of thrombospondin 1, J Cell Biol, vol.130, pp.503-506, 1995.

H. Braak, D. Tredici, and K. , Cortico-basal ganglia-cortical circuitry in Parkinson's disease reconsidered, Exp Neurol, vol.212, pp.226-229, 2008.

R. A. Brekken and E. H. Sage, SPARC, a matricellular protein: at the crossroads of cell-matrix, Matrix Biol, vol.19, pp.569-580, 2000.

J. D. Cahoy, B. Emery, and A. Kaushal, A transcriptome database for astrocytes, neurons, and oligodendrocytes: a new resource for understanding brain development and function, J Neurosci, vol.28, pp.264-278, 2008.

M. R. Celio, Calbindin D-28 k and parvalbumin in the rat nervous system, Neuroscience, vol.35, issue.90, p.90091, 1990.

M. Chazalon, S. Dumas, and J. F. Bernard, The GABAergic Gudden's dorsal tegmental nucleus: a new relay for serotonergic regulation of sleep-wake behavior in the mouse, Neuropharmacology, vol.138, pp.315-330, 2018.

D. J. Christoffel, S. A. Golden, and D. Dumitriu, IkappaB kinase regulates social defeat stress-induced synaptic and behavioral plasticity, J Neurosci, vol.31, pp.314-321, 2011.

D. J. Christoffel, S. A. Golden, and J. J. Walsh, Excitatory transmission at thalamo-striatal synapses mediates susceptibility to social stress, Nat Neurosci, vol.18, pp.962-964, 2015.

B. M. Chronwall, D. A. Dimaggio, V. J. Massari, V. M. Pickel, D. A. Ruggiero et al., The anatomy of neuropeptide-Y-containing neurons in rat brain, Neuroscience, vol.15, pp.1159-1181, 1985.

A. A. Chubykin, D. Atasoy, M. R. Etherton, N. Brose, E. T. Kavalali et al., Activity-dependent validation of excitatory versus inhibitory synapses by neuroligin-1 versus neuroligin-2, Neuron, vol.54, pp.919-931, 2007.

A. Clemente-perez, S. R. Makinson, and B. Higashikubo, Distinct thalamic reticular cell types differentially modulate normal and pathological cortical rhythms, Cell Rep, vol.19, pp.2130-2142, 2017.

Q. Cui, J. E. Pitt, and A. Pamukcu, Blunted mGluR activation disinhibits striatopallidal transmission in parkinsonian mice, Cell Rep, vol.17, pp.2431-2444, 2016.

J. G. Emsley and J. D. Macklis, Astroglial heterogeneity closely reflects the neuronal-defined anatomy of the adult murine CNS, Neuron Glia Biol, vol.2, p.2, 2006.

A. M. Erdozain, S. De-gois, and V. Bernard, Structural and functional characterization of the interaction of snapin with the dopamine transporter: differential modulation of psychostimulant actions, Neuropsychopharmacology, vol.43, pp.1041-1051, 2018.

C. Eroglu, The role of astrocyte-secreted matricellular proteins in central nervous system development and function, J Cell Commun Signal, vol.3, pp.167-176, 2009.

J. P. Girard and T. A. Springer, Cloning from purified high endothelial venule cells of hevin, a close relative of the antiadhesive extracellular matrix protein SPARC, Immunity, vol.2, pp.90083-90090, 1995.

J. P. Girard and T. A. Springer, Modulation of endothelial cell adhesion by hevin, an acidic protein associated with high endothelial venules, J Biol Chem, vol.271, pp.4511-4517, 1996.

V. Gongidi, C. Ring, M. Moody, R. Brekken, E. H. Sage et al., SPARC-like 1 regulates the terminal phase of radial glia-guided migration in the cerebral cortex, Neuron, vol.41, pp.57-69, 2004.

H. O. Hambrock, D. P. Nitsche, U. Hansen, P. Bruckner, M. Paulsson et al., SC1/hevin. An extracellular calciummodulated protein that binds collagen I, J Biol Chem, vol.278, pp.11351-11358, 2003.

B. N. Hammack, K. Y. Fung, S. W. Hunsucker, M. W. Duncan, M. P. Burgoon et al., Proteomic analysis of multiple sclerosis cerebrospinal fluid, Mult Scler, vol.10, pp.245-260, 2004.

N. Hashimoto, T. Sato, and T. Yajima, SPARCL1-containing neurons in the human brainstem and sensory ganglion, Somatosens Mot Res, vol.33, p.15, 2016.

S. Herculano-houzel, The glia/neuron ratio: how it varies uniformly across brain structures and species and what that means for brain physiology and evolution, Glia, vol.62, pp.1377-1391, 2014.

E. Herzog, G. C. Bellenchi, and C. Gras, The existence of a second vesicular glutamate transporter specifies subpopulations of glutamatergic neurons, J Neurosci, vol.21, p.181, 2001.

G. W. Huntley, Synaptic circuit remodelling by matrix metalloproteinases in health and disease, Nat Rev Neurosci, vol.13, pp.743-757, 2012.

N. T. Ingolia, S. Ghaemmaghami, J. R. Newman, and J. S. Weissman, Genome-wide analysis in vivo of translation with nucleotide resolution using ribosome profiling, Science, vol.324, pp.218-223, 2009.

O. Johansson, T. Hokfelt, and R. P. Elde, Immunohistochemical distribution of somatostatin-like immunoreactivity in the central nervous system of the adult rat, Neuroscience, vol.13, pp.265-339, 1984.

I. G. Johnston, T. Paladino, J. W. Gurd, and I. R. Brown, Molecular cloning of SC1: a putative brain extracellular matrix glycoprotein showing partial similarity to osteonectin/BM40/SPARC, Neuron, vol.4, pp.165-176, 1990.

E. V. Jones, Y. Bernardinelli, Y. C. Tse, S. Chierzi, T. P. Wong et al., Astrocytes control glutamate receptor levels at developing synapses through SPARC-beta-integrin interactions, J Neurosci, vol.31, pp.4154-4165, 2011.

H. Kucukdereli, N. J. Allen, and A. T. Lee, Control of excitatory CNS synaptogenesis by astrocyte-secreted proteins Hevin and SPARC, Proc Natl Acad Sci, vol.108, pp.440-449, 2011.

S. Lively and I. R. Brown, Extracellular matrix protein SC1/hevin in the hippocampus following pilocarpine-induced status epilepticus, J Neurochem, vol.107, pp.1335-1346, 2008.

S. Lively and I. R. Brown, The extracellular matrix protein SC1/ hevin localizes to excitatory synapses following status epilepticus in the rat lithium-pilocarpine seizure model, J Neurosci Res, vol.86, pp.2895-2905, 2008.

S. Lively and I. R. Brown, Localization of the extracellular matrix protein SC1 coincides with synaptogenesis during rat postnatal development, Neurochem Res, vol.33, pp.1692-1700, 2008.

S. Lively, I. Moxon-emre, and L. C. Schlichter, SC1/hevin and reactive gliosis after transient ischemic stroke in young and aged rats, J Neuropathol Exp Neurol, vol.70, pp.913-929, 2011.

S. Lloyd-burton and A. J. Roskams, SPARC-like 1 (SC1) is a diversely expressed and developmentally regulated matricellular protein that does not compensate for the absence of SPARC in the CNS, J Comp Neurol, vol.520, pp.2575-2590, 2012.

I. Markiewicz and B. Lukomska, The role of astrocytes in the physiology and pathology of the central nervous system, Acta Neurobiol Exp (Wars), vol.66, pp.343-358, 2006.

P. J. Mckinnon, S. K. Mclaughlin, M. Kapsetaki, and R. F. Margolskee, Extracellular matrix-associated protein Sc1 is not essential for mouse development, Mol Cell Biol, vol.20, pp.656-660, 2000.

P. Mendez and A. Bacci, Assortment of GABAergic plasticity in the cortical interneuron melting pot, Neural Plast, 2011.

D. B. Mendis, L. Malaval, and I. R. Brown, SPARC, an extracellular matrix glycoprotein containing the follistatin module, is expressed by astrocytes in synaptic enriched regions of the adult brain, Brain Res, vol.676, pp.69-79, 1995.

D. B. Mendis, S. Shahin, J. W. Gurd, and I. R. Brown, SC1, a SPARC-related glycoprotein, exhibits features of an ECM component in the developing and adult brain, Brain Res, vol.713, pp.53-63, 1996.

D. B. Mendis, G. O. Ivy, and I. R. Brown, Induction of SC1 mRNA encoding a brain extracellular matrix glycoprotein related to SPARC following lesioning of the adult rat forebrain, Neurochem Res, vol.25, pp.1637-1644, 2000.

L. Morel, M. Chiang, and H. Higashimori, Molecular and Functional Properties of Regional Astrocytes in the Adult Brain, J Neurosci, vol.37, pp.8706-8717, 2017.

A. J. Mothe and I. R. Brown, Effect of hyperthermia on the transport of mRNA encoding the extracellular matrix glycoprotein SC1 into Bergmann glial cell processes, Brain Res, vol.931, issue.02, pp.2270-2279, 2002.

J. E. Murphy-ullrich and E. H. Sage, Revisiting the matricellular concept, Matrix Biol, vol.37, pp.1-14, 2014.

M. Nedergaard, B. Ransom, and S. A. Goldman, New roles for astrocytes: redefining the functional architecture of the brain, Trends Neurosci, vol.26, pp.523-530, 2003.

H. Nishida and S. Okabe, Direct astrocytic contacts regulate local maturation of dendritic spines, J Neurosci, vol.27, pp.4466-4472, 2007.

A. Panatier, D. T. Theodosis, J. P. Mothet, B. Touquet, L. Pollegioni et al., Glia-derived D-serine controls NMDA receptor activity and synaptic memory, Cell, vol.125, pp.775-784, 2006.
URL : https://hal.archives-ouvertes.fr/inserm-00078312

G. Paxinos, K. Franklin, S. D. Academic, J. S. Polepalli, H. Wu et al., Modulation of excitation on parvalbumin interneurons by neuroligin-3 regulates the hippocampal network, Nat Neurosci, vol.20, pp.219-229, 2001.

W. C. Risher, S. Patel, and I. H. Kim, Astrocytes refine cortical connectivity at dendritic spines, 2014.

J. Rossier, A. Bernard, and J. H. Cabungcal, Cortical fast-spiking parvalbumin interneurons enwrapped in the perineuronal net express the metallopeptidases Adamts8, Adamts15 and Neprilysin, Mol Psychiatry, vol.20, pp.154-161, 2015.

E. H. Sage and P. Bornstein, Extracellular proteins that modulate cellmatrix interactions-sparc, tenascin, and thrombospondin, J Biol Chem, vol.266, pp.14831-14834, 1991.

M. Savasta, J. M. Palacios, and G. Mengod, Regional localization of the mRNA coding for the neuropeptide cholecystokinin in the rat brain studied by in situ hybridization, Neurosci Lett, vol.93, p.90086, 1988.

A. Schmitt, E. Asan, B. Puschel, and P. Kugler, Cellular and regional distribution of the glutamate transporter GLAST in the CNS of rats: nonradioactive in situ hybridization and comparative immunocytochemistry, J Neurosci, vol.17, pp.1-10, 1997.

N. Schweizer, S. Pupe, and E. Arvidsson, Limiting glutamate transmission in a Vglut2-expressing subpopulation of the subthalamic nucleus is sufficient to cause hyperlocomotion, Proc Natl Acad Sci, vol.111, pp.7837-7842, 2014.

E. Shigetomi, E. A. Bushong, and M. D. Haustein, Imaging calcium microdomains within entire astrocyte territories and endfeet with GCaMPs expressed using adeno-associated viruses, J Gen Physiol, vol.141, pp.633-647, 2013.

S. K. Singh, J. A. Stogsdill, and N. S. Pulimood, Astrocytes assemble thalamocortical synapses by bridging NRX1alpha and NL1 via Hevin, Cell, vol.164, pp.183-196, 2016.

J. A. Soderling, M. J. Reed, A. Corsa, and E. H. Sage, Cloning and expression of murine SC1, a gene product homologous to SPARC, J Histochem Cytochem, vol.45, p.607, 1997.

J. L. Stobart, K. D. Ferrari, M. Barrett, C. Gluck, M. J. Stobart et al., Cortical circuit activity evokes rapid astrocyte calcium signals on a similar timescale to neurons, Neuron, vol.98, pp.726-735, 2018.

M. M. Sullivan, P. A. Puolakkainen, T. H. Barker, S. E. Funk, and E. H. Sage, Altered tissue repair in hevin-null mice: inhibition of fibroblast migration by a matricellular SPARC homolog, Wound Repair Regen, vol.16, pp.310-319, 2008.

J. M. Tepper, F. Tecuapetla, T. Koos, and O. Ibanez-sandoval, Heterogeneity and diversity of striatal GABAergic interneurons, Front Neuroanat, vol.4, p.150, 2010.

R. Ventura and K. M. Harris, Three-dimensional relationships between hippocampal synapses and astrocytes, J Neurosci, vol.19, pp.19-35, 1999.

V. Vialou, L. Balasse, S. Dumas, B. Giros, and S. Gautron, Neurochemical characterization of pathways expressing plasma membrane monoamine transporter in the rat brain, Neuroscience, vol.144, pp.616-622, 2007.
URL : https://hal.archives-ouvertes.fr/inserm-02008095

V. Vialou, A. J. Robison, and Q. C. Laplant, DeltaFosB in brain reward circuits mediates resilience to stress and antidepressant responses, Nat Neurosci, vol.13, pp.745-752, 2010.

T. Viereckel, S. Dumas, and C. J. Smith-anttila, Midbrain gene screening identifies a new mesoaccumbal glutamatergic pathway and a marker for dopamine cells neuroprotected in Parkinson's disease, Sci Rep, vol.6, p.35203, 2016.

A. J. Vincent, P. W. Lau, and A. J. Roskams, SPARC is expressed by macroglia and microglia in the developing and mature nervous system, Dev Dyn, vol.237, pp.1449-1462, 2008.
DOI : 10.1002/dvdy.21563

URL : https://onlinelibrary.wiley.com/doi/pdf/10.1002/dvdy.21563

M. S. Weaver, G. Workman, M. Cardo-vila, W. Arap, R. Pasqualini et al., Processing of the matricellular protein hevin in mouse brain is dependent on ADAMTS4, J Biol Chem, vol.285, pp.5868-5877, 2010.

M. Weaver, G. Workman, C. R. Schultz, N. Lemke, S. A. Rempel et al., Proteolysis of the matricellular protein hevin by matrix metalloproteinase-3 produces a SPARC-like fragment (SLF) associated with neovasculature in a murine glioma model, J Cell Biochem, 2011.

G. N. Yin, H. W. Lee, J. Y. Cho, and K. Suk, Neuronal pentraxin receptor in cerebrospinal fluid as a potential biomarker for neurodegenerative diseases, Brain Res, vol.1265, pp.158-170, 2009.

A. Zeisel, A. B. Munoz-manchado, and S. Codeluppi, Brain structure. Cell types in the mouse cortex and hippocampus revealed by singlecell RNA-sEq, Science, vol.347, pp.1138-1142, 2015.

V. Zhurov, J. D. Stead, and Z. Merali, Molecular pathway reconstruction and analysis of disturbed gene expression in depressed individuals who died by suicide, PLoS One, vol.7, p.81, 2012.