Menu
Neonatal leptin antagonism improves metabolic programming of postnatally overnourished mice. Int J Obes (Lond). 2022 Jun;46(6):1138-1144. doi: 10.1038/s41366-022-01093-4. Epub 2022 Feb 16. PMID: 35173277
Melatonin drugs inhibit SARS-CoV-2 entry into the brain and virus-induced damage of cerebral small vessels. Cell Mol Life Sci. 2022 Jun 13;79(7):361. doi: 10.1007/s00018-022-04390-3.
Molecular control of the development of hypothalamic neurons involved in metabolic regulation.
Unveiling the Importance of Tanycytes in the Control of the Dialogue Between the Brain and the Periphery. Nampoothiri S, Duquenne M, Prevot V.
In: Tasker JG, et al., ed. Glial-Neuronal Signaling in Neuroendocrine Systems. Masterclass in Neuroendocrinology Series. Switzerland: Springer Nature:255-284, 2021.
The proportion of cleaved anti-Müllerian hormone is higher in serum but not follicular fluid of obese women independently of polycystic ovary syndrome. Peigné M., Pigny1 P., Pankhurst M.W., Drumez E., Loyens A., Dewailly D., Catteau-Jonard S., Giacobini P. Reproductive BioMedicine Online 2020 , 41:1112-1121. DOI: 10.1016/j.rbmo.2020.07.020.
The endoplasmic reticulum stress-autophagy pathway controls hypothalamic development and energy balance regulation in leptin-deficient neonates. Park S, Aintablian A, Coupe B, Bouret SG Nat Commun 2020. 11, 1914
Maternal obesity-induced endoplasmic reticulum stress causes metabolic alterations and abnormal hypothalamic development in the offspring. Park S, Jang A, Bouret SG PLoS Biol 2020. 18, e3000296
Hypothalamic Structural and Functional Imbalances in Anorexia Nervosa. Florent V, Baroncini M, Jissendi-Tchofo P, Lopes R, Vanhoutte M, Rasika S, Pruvo JP, Vignau J, Verdun S, Johansen JE, Pigeyre M, Bouret SG, Nilsson IAK, Prevot V. Neuroendocrinology. 2020. 110, 552-562.
Animal Models to Understand the Etiology and Pathophysiology of Polycystic Ovary Syndrome. Stener-Victorin E, Padmanabhan V, Walters KA, Campbell RE, Benrick A, Giacobini P, Dumesic DA, Abbott DH. Endocr Rev. 2020. 41, 538-76.
Human Semaphorin 3 Variants Link Melanocortin Circuit Development and Energy Balance. Van der Klaauw AA, Croizier S, Mendes de Oliveira E, Stadler LKJ, Park S, Kong Y, Banton MC, Tandon P, Hendricks AE, Keogh JM, Riley SE, Papadia S, Henning E, Bounds R, Bochukova EG, Mistry V, O’Rahilly S, Simerly RB, Consortium UK, , Minchin, J.E.N., Barroso, I., Jones, E.Y., Bouret, S.G. & Farooqi, I.S. Cell 2019. 176: 729-742 e18
Non-nutritive Sweeteners Induce Hypothalamic ER Stress Causing Abnormal Axon Outgrowth. Park, S., Sethi, S. & Bouret, S.G. Front Endocrinol (Lausanne) 2019. 10, 876.
Defective AMH signaling disrupts GnRH neuron development and function and contributes to hypogonadotropic hypogonadism. Malone, S.A., Papadakis, G.E., Messina, A., Mimouni, N.E.H., Trova, S., Imbernon, M., Allet, C., Cimino, I., Acierno, J., Cassatella, D., Xu, C., Quinton, R., Szinnai, G., Pigny, P., Alonso-Cotchico, L., Masgrau, L., Marechal, J.D., Prevot, V., Pitteloud, N. & Giacobini, P. Elife 2019. 8: e47198.
Defective AMH signaling disrupts GnRH neuron development and function and contributes to hypogonadotropic hypogonadism. Malone SA, Papadakis GE, Messina A, Mimouni NEH, Trova S, Imbernon M, Allet C, Cimino I, Acierno J, Cassatella D, Xu C, Quinton R, Szinnai G, Pigny P, Alonso-Cotchico L, Masgrau L, Maréchal JD, Prevot V, Pitteloud N, Giacobini P. Elife. 2019. 8:e47198. doi: 10.7554/eLife.47198
Human Semaphorin 3 Variants Link Melanocortin Circuit Development and Energy Balance. van der Klaauw AA, Croizier S, Mendes de Oliveira E, Stadler LKJ, Park S, Kong Y, Banton MC, Tandon P, Hendricks AE, Keogh JM, Riley SE, Papadia S, Henning E, Bounds R, Bochukova EG, Mistry V, O’Rahilly S, Simerly RB; INTERVAL; UK10K Consortium, Minchin JEN, Barroso I, Jones EY, Bouret SG, Farooqi IS. Cell. 2019. 176:729-742.e18. doi: 10.1016/j.cell.2018.12.009
Emerging Roles of Anti-Müllerian Hormone in Hypothalamic-Pituitary Function. Barbotin AL, Peigné M, Malone SA, Giacobini P. Neuroendocrinology. 2019. 109,218-229.
Role of astrocytes, microglia, and tanycytes in brain control of systemic metabolism. García-Cáceres C, Balland E, Prevot V, Luquet S, Woods SC, Koch M, Horvath TL, Yi CX, Chowen JA, Verkhratsky A, Araque A, Bechmann I, Tschöp MH. Nat Neurosci. 2019. 22,7-14.
Emerging Roles of Anti-Müllerian Hormone in Hypothalamic-Pituitary Function. Barbotin AL, Peigné M, Malone SA, Giacobini P Neuroendocrinology. 2019. doi: 10.1159/000500689.
Don’t Trust Your Gut: When Gut Microbiota Disrupt Fertility. Silva MSB, Giacobini P. Cell Metab. 2019, 30:616-618. doi: 10.1016/j.cmet.2019.09.005.
New Developments in Reproductive and Stress Neuroendocrinology. Prevot V, Millar RP. Neuroendocrinology. 2019, 109:191-192. doi: 10.1159/000502420.
Central Dicer-miR-103/107 controls developmental switch of POMC progenitors into NPY neurons and impacts glucose homeostasis. Croizier, S., Park, S., Maillard, J. & Bouret, S.G. Elife 2018. 7: e40429
Elevated prenatal anti-Müllerian hormone reprograms the fetus and induces polycystic ovary syndrome in adulthood Tata B, Mimouni NEH, Barbotin AL, Malone SA, Loyens A, Pigny P, Dewailly D, Catteau-Jonard S, Sundström-Poromaa I, Piltonen TT, Dal Bello F, Medana C, Prevot V, Clasadonte J, Giacobini P. Nat Med. 2018. doi: 10.1038/s41591-018-0035-5.
A comparative study of the neural stem cell niche in the adult hypothalamus of human, mouse, rat and grey mouse lemur (Microcebus murinus) Pellegrino G, Trubert C, Terrien J, Pifferi F, Leroy D, Loyens A, Migaud M, Baronicini M, Maurage CA, Fontaine C, Prevot V, Sharif A J Comp Neurol. 2018. 526(9):1419-1443
Elevated prenatal anti-Müllerian hormone reprograms the fetus and induces polycystic ovary syndrome in adulthood Tata BK, Mimouni NEH, Barbotin AL, Malone SA, Loyens A, Pigny P, Dewailly D, Catteau-Jonard S, Sundström-Poromaa I, Piltonen TT, Dal Bello F, Medana C, Prevot V, Classadonte J, Giacobini P Nature Medicine. 2018. doi:10.1038/s41591-018-0035-5
A comparative study of the neural stem cell niche in the adult hypothalamus of human, mouse, rat and grey mouse lemur (Microcebus murinus) Pellegrino G, Trubert C, Terrien J, Pifferi F, Leroy D, Loyens A, Migaud M, Baronicini M, Maurage CA, Fontaine C, Prevot V, Sharif A J Comp Neurol. 2018. doi: 10.1002/cne.24376
Central Dicer-miR-103/107 controls developmental switch of POMC progenitors into NPY neurons and impacts glucose homeostasis. Croizier S, Park S, Maillard J, Bouret SG. Elife. 2018. doi: 10.7554/eLife.40429.
Wired for eating: how is an active feeding circuitry established in the postnatal brain Muscatelli F, Bouret SG. Curr Opin Neurobiol. 2018. 52, 165-171.
Sex and gender differences in developmental programming of metabolism. Dearden L, Bouret SG, Ozanne SE. Mol Metab. 2018.15, 8-19.
The special relationship: glia-neuron interactions in the neuroendocrine hypothalamus Clasadonte J & Prevot V Nature Reviews Endocrinology. 2018, 14:25-44.
The versatile tanycyte: a hypothalamic integrator of reproduction and energy metabolism Prevot, V., B. Dehouck, A. Sharif, P. Ciofi, P. Giacobini, and J. Clasadonte. Endocrine Reviews. 2018. doi: 10.1210/er.2017-00235.
The versatile tanycyte: a hypothalamic integrator of reproduction and energy metabolism Prevot V, Dehouck B, Sharif A, Ciofi P, Giacobini P, Clasadonte J Endocrine Reviews. 2018. 1;39(3):333-368. doi: 10.1210/er.2017-00235
The special relationship: glia-neuron interactions in the neuroendocrine hypothalamus Clasadonte J & Prevot V Nature Reviews Endocrinology. 2018, doi:10.1038/nrendo.2017.124
Unveiling the Importance of Glia and Vascular Endothelial Cells in the Control of GnRH Neuronal Function Prevot V & Sharif A Herbison AE & Plant TM. The GnRH neuron and its Control. Wiley. Chapter 10, pp 225. doi 10.1002/9781119233275.ch10
Rôle des réseaux astrocytaires métaboliques dans le maintien de l’éveil Clasadonte J Med Sci (Paris) 2017; 34(3):199-202
Connexin 43-Mediated Astroglial Metabolic Networks Contribute to the Regulation of the Sleep-Wake Cycle Clasadonte, J., E. Scemes, Z. Wang, D. Boison, and P.G. Haydon. Neuron. 2017. 95:1365-1380.e5.
Phenotyping of nNOS Neurons in the Postnatal and Adult Female Mouse Hypothalamus Chachlaki K, Malone SA, Qualls-Creekmore, Hrabovszky E, Munzberg H, Giacobini P, Ango F, Prevot V J Comp Neurol, 2017. 525:3177-3189
Tridimensional Visualization and Analysis of Early Human Development Belle M, Godefroy D, Couly G, Malone SA, Collier F, Giacobini P, Chedotal A Cell. 2017. 169:161-173 e112
Phenotyping of nNOS Neurons in the Postnatal and Adult Female Mouse Hypothalamus Chachlaki K, Malone SA, Qualls-Creekmore, Hrabovszky E, Munzberg H, Giacobini P, Ango F, Prevot V J Comp Neurol. 2017. 10.1002/cne.24257
Tridimensional Visualization and Analysis of Early Human Development Belle M, Godefroy D, Couly G, Malone SA, Collier F, Giacobini P, Chedotal A Cell. 2017 DOI: http://dx.doi.org/10.1016/j.cell.2017.03.008
The gentle art of saying NO: how nitric oxide gets things done in the hypothalamus Chachlaki K, Garthwaite J, Prevot V Nature Reviews Endocrinology. 2017, 13:521-535.
When size matters: how astrocytic processes shape metabolism Sharif A, Prevot V Cell Metabolism. 2017, 25:995-996.
The gentle art of saying NO: how nitric oxide gets things done in the hypothalamus Chachlaki K, Garthwaite J, Prevot V Nature Reviews Endocrinology. 2017, doi:10.1038/nrendo.2017.69
Connecting metabolism and gonadal function: Novel central neuropeptide pathways involved in the metabolic control of puberty and fertility Manfredi-Lozano M, Roa J, Tena-Sempere M Frontiers in Neuroendocrinology. 2017, doi: 10.1016/j.yfrne.2017.07.008
When size matters: how astrocytic processes shape metabolism Sharif A, Prevot V Cell Metabolism. 2017, doi:10.1016/j.cmet.2017.04.016
Les micro-ARN Nouveaux acteurs du contrôle hypothalamique de la fertilité Messina A, Langlet F, Prevot V Med Sci (Paris) 2017; 33:506-511
Tanycytes hypothalamiques, barrière hématoencéphalique et rôle dans la régulation de l’homéostasie énergétique Florent V, Baroncini M, Prevot V Cahiers de Nutrition et de Diététique, 52)1):26-32
Développement des neurones à GnRH dans le cerveau d’embryons humains Barbotin AL, Prevot V, Giacobini P Medi Sci (Pari) 2017; 33:376-379
Loss of Magel2 impairs the development of hypothalamic Anorexigenic circuits Maillard J, Park S, Croizier S, Vanacker C, Cook JH, Prevot V, Tauber M, and Bouret Hum Mol Genet. 25:3208-3215, 2016
A microRNA switch regulates the rise in hypothalamic GnRH production before puberty Messina A, Langlet F, Chachlaki K, Roa J, Rasika S, Jouy N, Gallet S, Gaytan F, Parkash J, Tena-Sempere M, Giacobini P, Prevot V Nat Neurosci. 2016 19, 835-844 doi:10.1038/nn.4298
Novel role for anti-Müllerian hormone in the regulation of GnRH neuron excitability and hormone secretion Cimino I, Casoni F, Liu X, Messina A, Parkash J, Soazik P, Catteau-Jonard S, Collier F, Baroncini M, Dewailly D, Pigny P, Prescott M, Campbell R, Herbison A, Prevot V, Giacobini P Nat Commun. 2016, 7:10055
Hypothalamic microRNAs flip the switch for fertility Messina A, Prevot V Oncotarget. 2016, DOI: 10.18632/oncotarget.14646
Reproduction: A kiss to set the rhythm Shruti S, Prevot V elife. 2016, doi:e19823
Programming the Brain from the Womb: Maternal Obesity Perturbs the Hypothalamic Blood-Brain Barrier Duquenne, M., Dehouck, B. & Prevot, V Endocrinology, 157:2201-2203, 2016
Coexpression profiles reveal hidden gene networks Chachlaki & Prevot PNAS (doi: 10.1073/pnas.1600717113)
Ontogeny of Neuroendocrine Feeding Circuits Croizier S & Bouret SG Dickson SL, Mercer JG (eds) Neuroendocrinology of Appetite. Wiley & Sons Ltd, c3
Control of fertility: New player identified Anti-Mullerian hormone: an ovarian hormone exerting hypothalamic feedback? Catteau-Jonard S, Dewailly D, Prevot V, Cimino I & Giacobini P Med Sci (Paris), 32:441-444, 2016 Maternal obesity alters social brain programming by altering gut microbiota in progeny Barbotin AL, Giacobini P, Prévot V Med Sci (Paris). 32930-932, 2016
European Consensus Statement on congenital hypogonadotropic hypogonadism—pathogenesis, diagnosis and treatment Boehm U., Bouloux P.M., Dattani M.T., de Roux N., Dodé C., Dunkel L., Dwyer A.A., Giacobini P., Hardelin JP., Juul A., Maghnie M., Pitteloud N., Prevot V., Raivio T., Tena-Sempere M., Quinton R. and Young J. (2015). Nature Reviews Endocrinology (doi:10.1038/nrendo.2015.112)
Shaping the Reproductive System: Role of Semaphorins in Gonadotropin-Releasing Hormone Development and Function Giacobini, P Neuroendocrinology 102, 200-215, 2015
Gene-environment interactions controlling energy and glucose homeostasis and the developmental origins of obesity Bouret, S., Levin, B.E. & Ozanne, S.E Physiol Rev 95, 47-82, 2015
Endothelial cell plasticity in the normal and injured central nervous system Vanacker C, Sharif A, Prevot P Chapter 4, CRC Press, 2015
Leptin dependent neuronal NO signaling in the preoptic hypothalamus facilitates reproduction Bellefontaine N, Chachlaki K, Parkash J, Vanaker C, Colledge W, d’Anglemont de Tassigny X, Garthwaite J, Bouret SG, Prevot V. J Clin Invest 124:2550-2559, 2014.
Brain Endothelial Cells Control Fertility through Ovarian-Steroid_dependent Release of Semaphorin 3A Giacobini P, Parkash J, Campagne C, Messina A, Casoni F, Vanacker C, Langlet F, Hobo B, Cagnoni G, Gallet S, Hanchate NK, Mazur D, Taniguchi M, Mazzone M, Verhaagen J, Ciofi P, Bouret SG, Tamagnone L, Prevot V. PLoS Biology 12(3):e1001808, 2014.
Hypothalamic tanycytes are an ERK-gated conduit for leptin into the brain Balland E, Dam J, Langlet F, Caron E, Steculorum S, Falluel-Morel A, Anouar Y, Dehouck B, Trinquet E, Jockers R, Bouret SG, Prevot V. Hypothalamic tanycytes are an ERK-gated conduit for leptin into the brain. Cell Metab 19, 293-301, 2014. (also Cell Metab Previews p. 173-175)
Tanycytes: a gateway to the metabolic hypothalamus Langlet, F J Neuroendocrinol 26, 753-760, 2014
Neurogenesis and gliogenesis in the postnatal hypothalamus: a new level of plasticity for the regulation of hypothalamic function Sharif A, Ojeda SR, Prevot V Junier MP, Kernie SG eds. Endogenous Stem Cell-Based Brain Remodeling in Mammals, Stem Cell Biology and Regenerative Medicine. New York: Springer Science+Business Media, Chapter 6, pp 105-136, 2014
Tanycyte-like cells form a blood-cerebrospinal fluid barrier in the circumventricular organs of the mouse brain Langlet F, Muller A, Bouret SG, Prevot V, Dehouck B. J Comp Neurol. 2013521(15):3389-405 doi: 10.1002/cne.23355
Tanycytic VEGF-A boosts blood-hypothalamus barrier plasticity and access of metabolic signals to the arcuate nucleus in response to fasting Langlet F, Levin BE, Luquet S, Mazzone M, Messina A, Dunn-Meynell AA, Balland E, Lacombe A, Mazur D, Carmeliet P, Bouret SG, Prevot V, Dehouck B . Cell Metab. 2013 Apr 2;17(4):607-17. doi: 10.1016/j.cmet.2013.03.004..
Rapid sensing of circulating ghrelin by hypothalamic appetite-modifying neurons Schaeffer M, Langlet F, Lafont C, Molino F, Hodson DJ, Roux T, Lamarque L, Verdié P, Bourrier E, Dehouck B, Banères JL, Martinez J, Méry PF, Marie J, Trinquet E, Fehrentz JA, Prévot V, Mollard P. Proc Natl Acad Sci U S A. 2013 Jan 22;110(4):1512-7. doi:10.1073/pnas.1212137110.
Semaphorin signaling in the development and function of the gonadotropin hormone-releasing hormone system Messina A and Giacobini P Front. Endocrinol., 23 September 2013. doi: 10.3389/fendo.2013.00133, 2013
Flipping the tanycyte switch: how circulating signals gain direct access to the metabolic brain Prevot V, Langlet F, Dehouck B Aging 5:332-334, 2013
Semaphorins in the development, homeostasis and disease of hormone systems Giacobini P, Prevot V Semin Cell Dev Biol 24:190-198, 2013
Role of glia in the regulation of gonadotropin-releasing hormone neuronal activity and secretion Sharif A, Baroncini M, Prevot V Neuroendocrinology 98:1-15, 2013
Organizational actions of metabolic hormones Bouret, S.G Front Neuroendocrinol 34, 18-26, 2013
Suppression of β1-integrin in gonadotropin-releasing hormone cells disrupts migration and axonal extension resulting in severe reproductive alterations. Parkash J, Cimino I, Ferraris N, Casoni F, Wray S, Cappy H, Prevot V, Giacobini P. J Neurosci. 2012 Nov 21;32(47):16992-7002. doi: 10.1523/JNEUROSCI.3057-12.2012.
RIPping off GABA release in hypothalamic circuits causes obesity. Bouret SG. Cell Metab. 2012 Nov 7;16(5):557-8. doi: 10.1016/j.cmet.2012.10.014.
SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome. Hanchate NK, Giacobini P, Lhuillier P, Parkash J, Espy C, Fouveaut C, Leroy C, Baron S, Campagne C, Vanacker C, Collier F, Cruaud C, Meyer V, García-Piñero A, Dewailly D, Cortet-Rudelli C, Gersak K, Metz C, Chabrier G, Pugeat M, Young J, Hardelin JP, Prevot V, Dodé C. PLoS Genet. 2012 Aug;8(8):e1002896. doi: 10.1371/journal.pgen.1002896.
Alteration in neonatal nutrition causes perturbations in hypothalamic neural circuits controlling reproductive function. Caron E, Ciofi P, Prevot V, Bouret SG. J Neurosci. 2012 Aug 15;32(33):11486-94. doi: 10.1523/JNEUROSCI.6074-11.2012.
Embryonic birthdate of hypothalamic leptin-activated neurons in mice. Ishii Y, Bouret SG. Endocrinology. 2012 Aug;153(8):3657-67. doi: 10.1210/en.2012-1328.
Loss of autophagy in pro-opiomelanocortin neurons perturbs axon growth and causes metabolic dysregulation. Coupé B, Ishii Y, Dietrich MO, Komatsu M, Horvath TL, Bouret SG. Cell Metab. 2012 Feb 8;15(2):247-55. doi: 10.1016/j.cmet.2011.12.016.
Distinct roles for specific leptin receptor signals in the development of hypothalamic feeding circuits. Bouret SG, Bates SH, Chen S, Myers MG Jr, Simerly RB. J Neurosci. 2012 Jan 25;32(4):1244-52. doi: 10.1523/JNEUROSCI.2277-11.2012.
Kisspeptin-GPR54 signaling in mouse NO-synthesizing neurons participates in the hypothalamic control of ovulation. Hanchate NK, Parkash J, Bellefontaine N, Mazur D, Colledge WH, d’Anglemont de Tassigny X, Prevot V. J Neurosci. 2012 Jan 18;32(3):932-45. doi: 10.1523/JNEUROSCI.4765-11.2012.
MRI atlas of the human hypothalamus. Baroncini M, Jissendi P, Balland E, Besson P, Pruvo JP, Francke JP, Dewailly D, Blond S, Prevot V. Neuroimage. 2012 Jan 2;59(1):168-80. doi: 10.1016/j.neuroimage.2011.07.013.
Neuroendocrine control of reproduction Clarke IJ, Campbell R, Smith JT, Prevot V, Wray S In: Handbook of Neuroendocrinology (Fink G, Pfaff DW, Levine JE, Eds), Academic Press, San Diego, CA, Chapter 9, pp 197-235, 2012
Isolation and culture of human astrocytes Sharif A, Prevot V Methods Mol Biol 814:137-151, 2012
Dysregulation of Semaphorin7A/β1-integrin signaling leads to defective GnRH-1 cell migration, abnormal gonadal development and altered fertility. Messina A, Ferraris N, Wray S, Cagnoni G, Donohue DE, Casoni F, Kramer PR, Derijck AA, Adolfs Y, Fasolo A, Pasterkamp RJ, Giacobini P. Hum Mol Genet. 2011 Dec 15;20(24):4759-74. doi: 10.1093/hmg/ddr403.
Prostaglandin E2 release from astrocytes triggers gonadotropin-releasing hormone (GnRH) neuron firing via EP2 receptor activation. Clasadonte J, Poulain P, Hanchate NK, Corfas G, Ojeda SR, Prevot V. Proc Natl Acad Sci U S A. 2011 Sep 20;108(38):16104-9. doi: 10.1073/pnas.1107533108.
Maternal diabetes compromises the organization of hypothalamic feeding circuits and impairs leptin sensitivity in offspring. Steculorum SM, Bouret SG. Endocrinology. 2011 Nov;152(11):4171-9. doi: 10.1210/en.2011-1279.
Nitric oxide as key mediator of neuron-to-neuron and endothelia-to-glia communication involved in the neuroendocrine control of reproduction Bellefontaine N, Hanchate NK, Parkash J, Campagne C, de Seranno S, Clasadonte J, d’Anglemont de Tassigny X, Prevot V Neuroendocrinology 93:74-89, 2011
Gliotransmission by prostaglandin E2: a prerequisite for GnRH neuronal function Clasadonte J, Sharif A, Baroncini M, Prevot V Front Endocrinol 2:1-12, 2011
GnRH neurons directly listen to the peripher Prevot V Endocrinology 152: 3589-3591, 2011
Phosphorylation of N-methyl-D-aspartic acid receptor-associated neuronal nitric oxide synthase depends on estrogens and modulates hypothalamic nitric oxide production during the ovarian cycle. Parkash J, d’Anglemont de Tassigny X, Bellefontaine N, Campagne C, Mazure D, Buée-Scherrer V, Prevot V. Endocrinology. 2010 Jun;151(6):2723-35. doi: 10.1210/en.2010-0007.
Role of estradiol in the dynamic control of tanycyte plasticity mediated by vascular endothelial cells in the median eminence. De Seranno S, d’Anglemont de Tassigny X, Estrella C, Loyens A, Kasparov S, Leroy D, Ojeda SR, Beauvillain JC, Prevot V. Endocrinology. 2010 Apr;151(4):1760-72. doi: 10.1210/en.2009-0870.
Differential distribution of tight junction proteins suggests a role for tanycytes in blood-hypothalamus barrier regulation in the adult mouse brain. Mullier A, Bouret SG, Prevot V, Dehouck B. J Comp Neurol. 2010 Apr 1;518(7):943-62. doi: 10.1002/cne.22273.
Distribution of leptin-sensitive cells in the postnatal and adult mouse brain. Caron E, Sachot C, Prevot V, Bouret SG J Comp Neurol. 2010 Feb 15;518(4):459-76. doi: 10.1002/cne.22219.
Sex steroid hormones-related structural plasticity in the human hypothalamus. Baroncini M, Jissendi P, Catteau-Jonard S, Dewailly D, Pruvo JP, Francke JP, Prevot V. Neuroimage. 2010 Apr 1;50(2):428-33. doi: 10.1016/j.neuroimage.2009.11.074.
Plasticity of neuroendocrine systems Prevot V Eur J Neurosci 32:1987-1988, 2010
GnRH nerve terminals, tanycytes and neurohaemal junction remodeling in the adult median eminence: functional consequences for reproduction and dynamic role of vascular endothelial cells Prevot V, Bellefontaine N, Baroncini M, Sharif A, Hanchate NK, Parkash J, Campagne C, de Seranno S J Neuroendocrinol 22:639-649, 2010
Function-related structural plasticity of the GnRH system: a role for neuronal-glial-endothelial interactions Prevot V, Hanchate NK, Bellefontaine N, Sharif A, Parkash J, Estrella C, Allet C, de Seranno S, Campagne C, de Tassigny X, Baroncini M Front Neuroendocrinol 31:241-258, 2010
ErbB receptor signaling in astrocytes: a mediator of neuron-glia communication in the mature central nervous system Sharif A, Prevot V Neurochem Int 57:344-358, 2010