Serotonergic regulation of appetite and sodium appetite.


Journal

Journal of neuroendocrinology
ISSN: 1365-2826
Titre abrégé: J Neuroendocrinol
Pays: United States
ID NLM: 8913461

Informations de publication

Date de publication:
09 2023
Historique:
revised: 27 06 2023
received: 05 02 2023
accepted: 15 07 2023
medline: 27 9 2023
pubmed: 1 8 2023
entrez: 1 8 2023
Statut: ppublish

Résumé

Serotonin is a neurotransmitter that is synthesized and released from the brainstem raphe nuclei to affect many brain functions. It is well known that the activity of raphe serotonergic neurons is changed in response to the changes in feeding status to regulate appetite via the serotonin receptors. Likewise, changes in volume status are known to alter the activity of raphe serotonergic neurons and drugs targeting serotonin receptors were shown to affect sodium appetite. Therefore, the central serotonin system appears to regulate ingestion of both food and salt, although neural mechanisms that induce appetite in response to hunger and sodium appetite in response to volume depletion are largely distinct from each other. In this review, we discuss our current knowledge regarding the regulation of ingestion - appetite and sodium appetite - by the central serotonin system.

Identifiants

pubmed: 37525500
doi: 10.1111/jne.13328
doi:

Substances chimiques

Sodium 9NEZ333N27
Serotonin 333DO1RDJY

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13328

Informations de copyright

© 2023 British Society for Neuroendocrinology.

Références

Martin AM, Young RL, Leong L, et al. The diverse metabolic roles of peripheral serotonin. Endocrinology. 2017;158(5):1049-1063.
Jacobs BL, Azmitia EC. Structure and function of the brain serotonin system. Physiol Rev. 1992;72(1):165-229.
Jouvet M. Biogenic amines and the states of sleep. Science. 1969;163(3862):32-41.
Merens W, Willem Van der Does AJ, Spinhoven P. The effects of serotonin manipulations on emotional information processing and mood. J Affect Disord. 2007;103(1):43-62.
Morin LP. Serotonin and the regulation of mammalian circadian rhythmicity. Ann Med. 1999;31(1):12-33.
Li Y, Zhong W, Wang D, et al. Serotonin neurons in the dorsal raphe nucleus encode reward signals. Nat Commun. 2016;7(1):1-15.
Altman HJ, Normile HJ. Enhancement of the memory of a previously learned aversive habit following pre-test administration of a variety of serotonergic antagonists in mice. Psychopharmacology (Berl). 1986;90(1):24-27.
Sohn JW, Elmquist JK, Williams KW. Neuronal circuits that regulate feeding behavior and metabolism. Trends Neurosci. 2013;36(9):504-512.
Ishimura K, Takeuchi Y, Fujiwara K, Tominaga M, Yoshioka H, Sawada T. Quantitative analysis of the distribution of serotonin-immunoreactive cell bodies in the mouse brain. Neurosci Lett. 1988;91(3):265-270.
Walther DJ, Peter JU, Bashammakh S, et al. Synthesis of serotonin by a second tryptophan hydroxylase isoform. Science. 2003;299(5603):76.
Cardozo Pinto DF, Yang H, Pollak Dorocic I, et al. Characterization of transgenic mouse models targeting neuromodulatory systems reveals organizational principles of the dorsal raphe. Nat Commun. 2019;10(1):4633.
Raymond JR, Mukhin YV, Gelasco A, et al. Multiplicity of mechanisms of serotonin receptor signal transduction. Pharmacol Ther. 2001;92(2):179-212.
Fuller RW, Wong DT. Fluoxetine: A serotonergic appetite suppressant drug. Drug Dev Res. 1989;17(1):1-15.
Heisler LK, Cowley MA, Tecott LH, et al. Activation of central melanocortin pathways by fenfluramine. Science. 2002;297(5581):609-611.
Connolly HM, Crary JL, McGoon MD, et al. Valvular heart disease associated with fenfluramine-phentermine. N Engl J Med. 1997;337(9):581-588.
Xu Y, Jones JE, Kohno D, et al. 5-HT2CRs expressed by pro-opiomelanocortin neurons regulate energy homeostasis. Neuron. 2008;60(4):582-589.
Berglund ED, Liu C, Sohn JW, et al. Serotonin 2C receptors in pro-opiomelanocortin neurons regulate energy and glucose homeostasis. J Clin Invest. 2013;123(12):5061-5070.
Sharretts J, Galescu O, Gomatam S, Andraca-Carrera E, Hampp C, Yanoff L. Cancer risk associated with Lorcaserin - the FDA's review of the CAMELLIA-TIMI 61 trial. N Engl J Med. 2020;383(11):1000-1002.
Rouah-Rosilio M, Orosco M, Nicolaidis S. Serotoninergic modulation of sodium appetite in the rat. Physiol Behav. 1994;55(5):811-816.
Strazzullo P, Leclercq C. Sodium. Adv Nutr. 2014;5(2):188-190.
Wagman W. Sodium chloride deprivation: development of sodium chloride as a reinforcement. Science. 1963;140(3574):1403-1404.
Fregly M, Rowland N. Role of renin-angiotensin-aldosterone system in NaCl appetite of rats. Am J Physiol Regul Integr Comp Physiol. 1985;248(1):R1-R11.
Zardetto-Smith AM, Beltz TG, Johnson AK. Role of the central nucleus of the amygdala and bed nucleus of the stria terminalis in experimentally-induced salt appetite. Brain Res. 1994;645(1-2):123-134.
Scalera G, Spector AC, Norgren R. Excitotoxic lesions of the parabrachial nuclei prevent conditioned taste aversions and sodium appetite in rats. Behav Neurosci. 1995;109(5):997-1008.
Jarvie BC, Palmiter RD. HSD2 neurons in the hindbrain drive sodium appetite. Nat Neurosci. 2017;20(2):167-169.
Matsuda T, Hiyama TY, Niimura F, et al. Distinct neural mechanisms for the control of thirst and salt appetite in the subfornical organ. Nat Neurosci. 2017;20(2):230-241.
Blundell JE. Serotonin and appetite. Neuropharmacology. 1984;23:1537-1551.
Schwartz DH, McClane S, Hernandez L, Hoebel BG. Feeding increases extracellular serotonin in the lateral hypothalamus of the rat as measured by microdialysis. Brain Res. 1989;479(2):349-354.
Curzon G. Serotonin and appetite. Ann N Y Acad Sci. 1990;600:521-530.
Dahlstroem A, Fuxe K. Evidence for the existence of monoamine-containing neurons in the central nervous system. I. Demonstration of monoamines in the cell bodies of brain stem neurons. Acta Physiol Scand Suppl. 1964;Suppl 232:1-55.
Okaty BW, Freret ME, Rood BD, et al. Multi-scale molecular deconstruction of the serotonin neuron system. Neuron. 2015;88(4):774-791.
Takase LF, Nogueira MI. Patterns of fos activation in rat raphe nuclei during feeding behavior. Brain Res. 2008;1200:10-18.
Bhave VM, Nectow AR. The dorsal raphe nucleus in the control of energy balance. Trends Neurosci. 2021;44(12):946-960.
Aklan I, Sayar-Atasoy N, Deng F, et al. Dorsal raphe serotonergic neurons suppress feeding through redundant forebrain circuits. Mol Metab. 2023;69:101676.
Ye Q, Nunez J, Zhang X. Raphe serotonin projections dynamically regulate feeding behavior through targeting inhibitory circuits from rostral zona incerta to paraventricular thalamus. Mol Metab. 2022;66:101634.
Weissbourd B, Ren J, DeLoach KE, Guenthner CJ, Miyamichi K, Luo L. Presynaptic partners of dorsal raphe serotonergic and GABAergic neurons. Neuron. 2014;83(3):645-662.
Pollak Dorocic I, Fürth D, Xuan Y, et al. A whole-brain atlas of inputs to serotonergic neurons of the dorsal and median raphe nuclei. Neuron. 2014;83(3):663-678.
Ogawa SK, Cohen JY, Hwang D, Uchida N, Watabe-Uchida M. Organization of monosynaptic inputs to the serotonin and dopamine neuromodulatory systems. Cell Rep. 2014;8(4):1105-1118.
Zhou L, Liu MZ, Li Q, Deng J, Mu D, Sun YG. Organization of functional long-range circuits controlling the activity of serotonergic neurons in the dorsal raphe nucleus. Cell Rep. 2017;18(12):3018-3032.
Ren J, Isakova A, Friedmann D, et al. Single-cell transcriptomes and whole-brain projections of serotonin neurons in the mouse dorsal and median raphe nuclei. Elife. 2019;8:e49424.
Okaty BW, Sturrock N, Escobedo Lozoya Y, et al. A single-cell transcriptomic and anatomic atlas of mouse dorsal raphe Pet1 neurons. Elife. 2020;9:e55523.
Yoo ES, Yu J, Sohn JW. Neuroendocrine control of appetite and metabolism. Exp Mol Med. 2021;53(4):505-516.
Sakurai T, Amemiya A, Ishii M, et al. Orexins and orexin receptors: A family of hypothalamic neuropeptides and G protein-coupled receptors that regulate feeding behavior. Cell. 1998;92(4):573-585.
Luo SX, Huang J, Li Q, et al. Regulation of feeding by somatostatin neurons in the tuberal nucleus. Science. 2018;361(6397):76-81.
Freed WJ, Perlow MJ, Wyatt RJ. Calcitonin: inhibitory effect on eating in rats. Science. 1979;206(4420):850-852.
Sabatier N, Leng G, Menzies J. Oxytocin, feeding, and satiety. Front Endocrinol. 2013;4:35.
Hawkins MF. Central nervous system neurotensin and feeding. Physiol Behav. 1986;36(1):1-8.
Reid LD. Endogenous opioid peptides and regulation of drinking and feeding. Am J Clin Nutr. 1985;42(5):1099-1132.
Crawley JN. The role of galanin in feeding behavior. Neuropeptides. 1999;33(5):369-375.
Miyawaki K, Yamada Y, Ban N, et al. Inhibition of gastric inhibitory polypeptide signaling prevents obesity. Nat Med. 2002;8(7):738-742.
Xiao X, Yeghiazaryan G, Hess S, et al. Orexin receptors 1 and 2 in serotonergic neurons differentially regulate peripheral glucose metabolism in obesity. Nat Commun. 2021;12(1):5249.
Schneeberger M, Brice NL, Pellegrino K, et al. Pharmacological targeting of glutamatergic neurons within the brainstem for weight reduction. Nat Metab. 2022;4(11):1495-1513.
Nectow AR, Schneeberger M, Zhang H, et al. Identification of a brainstem circuit controlling feeding. Cell. 2017;170(3):429-442.
Hioki H, Nakamura H, Ma YF, et al. Vesicular glutamate transporter 3-expressing nonserotonergic projection neurons constitute a subregion in the rat midbrain raphe nuclei. J Comp Neurol. 2010;518(5):668-686.
Liu Z, Zhou J, Li Y, et al. Dorsal raphe neurons signal reward through 5-HT and glutamate. Neuron. 2014;81(6):1360-1374.
Bruschetta G, Jin S, Liu ZW, Kim JD, Diano S. MC4R signaling in dorsal raphe nucleus controls feeding, anxiety, and depression. Cell Rep. 2020;33(2):108267.
Han Y, Xia G, Srisai D, et al. Deciphering an AgRP-serotoninergic neural circuit in distinct control of energy metabolism from feeding. Nat Commun. 2021;12(1):3525.
Hansson C, Alvarez-Crespo M, Taube M, et al. Influence of ghrelin on the central serotonergic signaling system in mice. Neuropharmacology. 2014;79:498-505.
Anderberg RH, Richard JE, Eerola K, et al. Glucagon-like peptide 1 and its analogs act in the dorsal raphe and modulate central serotonin to reduce appetite and body weight. Diabetes. 2017;66(4):1062-1073.
Kliteneck MA, Wirtshafter D. Comparative studies of the ingestive behaviors produced by microinjections of muscimol into the midbrain raphe nuclei or the ventral tegmental area of the rat. Life Sci. 1988;42(7):775-782.
Mansur SS, Terenzi MG, Neto JM, Faria MS, Paschoalini MA. Alpha1 receptor antagonist in the median raphe nucleus evoked hyperphagia in free-feeding rats. Appetite. 2011;57(2):498-503.
Wu Q, Clark MS, Palmiter RD. Deciphering a neuronal circuit that mediates appetite. Nature. 2012;483(7391):594-597.
He Y, Cai X, Liu H, et al. 5-HT recruits distinct neurocircuits to inhibit hunger-driven and non-hunger-driven feeding. Mol Psychiatry. 2021;26(12):7211-7224.
Heisler LK, Jobst EE, Sutton GM, et al. Serotonin reciprocally regulates melanocortin neurons to modulate food intake. Neuron. 2006;51(2):239-249.
Celli J, Rappold G, Niesler B. The human serotonin type 3 receptor gene (HTR3A-E) allelic variant database. Hum Mutat. 2017;38(2):137-147.
Oh CM, Park S, Kim H. Serotonin as a new therapeutic target for diabetes mellitus and obesity. Diabetes Metab J. 2016;40(2):89-98.
Hopwood SE, Stamford JA. Multiple 5-HT1 autoreceptor subtypes govern serotonin release in dorsal and median raphé nuclei. Neuropharmacology. 2001;40(4):508-519.
Dourish CT, Hutson PH, Curzon G. Low doses of the putative serotonin agonist 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT) elicit feeding in the rat. Psychopharmacology (Berl). 1985;86(1):197-204.
Dill MJ, Shaw J, Cramer J, Sindelar DK. 5-HT1A receptor antagonists reduce food intake and body weight by reducing total meals with no conditioned taste aversion. Pharmacol Biochem Behav. 2013;112:1-8.
Adell A, Celada P, Artigas F. The role of 5-HT1B receptors in the regulation of serotonin cell firing and release in the rat brain. J Neurochem. 2001;79(1):172-182.
Bouwknecht JA, van der Gugten J, Hijzen TH, Maes RA, Hen R, Olivier B. Male and female 5-HT1B receptor knockout mice have higher body weights than wildtypes. Physiol Behav. 2001;74(4):507-516.
Li L, Wyler SC, León-Mercado LA, et al. Delineating a serotonin 1B receptor circuit for appetite suppression in mice. J Exp Med. 2022;219(8):e20212307.
Fox MA, French HT, LaPorte JL, Blackler AR, Murphy DL. The serotonin 5-HT 2A receptor agonist TCB-2: a behavioral and neurophysiological analysis. Psychopharmacology (Berl). 2010;212:13-23.
Kennett GA, Ainsworth K, Trail B, Blackburn TP. BW 723C86, a 5-HT2B receptor agonist, causes hyperphagia and reduced grooming in rats. Neuropharmacology. 1997;36(2):233-239.
Martin CK, Redman LM, Zhang J, et al. Lorcaserin, a 5-HT2C receptor agonist, reduces body weight by decreasing energy intake without influencing energy expenditure. J Clin Endocrinol Metab. 2011;96(3):837-845.
Gao Y, Yao T, Deng Z, et al. TrpC5 mediates acute leptin and serotonin effects via Pomc neurons. Cell Rep. 2017;18(3):583-592.
Vickers SP, Clifton PG, Dourish CT, Tecott LH. Reduced satiating effect of d-fenfluramine in serotonin 5-HT2C receptor mutant mice. Psychopharmacology (Berl). 1999;143:309-314.
Sohn JW, Xu Y, Jones JE, Wickman K, Williams KW, Elmquist JK. Serotonin 2C receptor activates a distinct population of arcuate pro-opiomelanocortin neurons via TRPC channels. Neuron. 2011;71(3):488-497.
Lüscher C, Slesinger PA. Emerging roles for G protein-gated inwardly rectifying potassium (GIRK) channels in health and disease. Nat Rev Neurosci. 2010;11(5):301-315.
Roepke TA, Smith AW, Rønnekleiv OK, Kelly MJ. Serotonin 5-HT2C receptor-mediated inhibition of the M-current in hypothalamic POMC neurons. Am J Physiol Endocrinol Metab. 2012;302(11):E1399-E1406.
Heisler LK, Pronchuk N, Nonogaki K, et al. Serotonin activates the hypothalamic-pituitary-adrenal axis via serotonin 2C receptor stimulation. J Neurosci. 2007;27(26):6956-6964.
Li MM, Madara JC, Steger JS, et al. The paraventricular hypothalamus regulates satiety and prevents obesity via two genetically distinct circuits. Neuron. 2019;102(3):653-667.
Yoo ES, Li L, Jia L, et al. Gαi/o-coupled Htr2c in the paraventricular nucleus of the hypothalamus antagonizes the anorectic effect of serotonin agents. Cell Rep. 2021;37(7):109997.
D'Agostino G, Lyons D, Cristiano C, et al. Nucleus of the solitary tract serotonin 5-HT2C receptors modulate food intake. Cell Metab. 2018;28(4):619-630.
Xu P, He Y, Cao X, et al. Activation of serotonin 2C receptors in dopamine neurons inhibits binge-like eating in mice. Biol Psychiatry. 2017;81(9):737-747.
Pratt WE, Lin P, Pierce-Messick Z, Ilesanmi AO, Clissold KA. Contrasting effects of 5-HT(3) receptor stimulation of the nucleus accumbens or ventral tegmentum on food intake in the rat. Behav Brain Res. 2017;323:15-23.
Jean A, Conductier G, Manrique C, et al. Anorexia induced by activation of serotonin 5-HT4 receptors is mediated by increases in CART in the nucleus accumbens. Proc Natl Acad Sci U S A. 2007;104(41):16335-16340.
Pratt WE, Blackstone K, Connolly ME, Skelly MJ. Selective serotonin receptor stimulation of the medial nucleus accumbens causes differential effects on food intake and locomotion. Behav Neurosci. 2009;123(5):1046-1057.
Kotańska M, Lustyk K, Bucki A, Marcinkowska M, Śniecikowska J, Kołaczkowski M. Idalopirdine, a selective 5-HT6 receptor antagonist, reduces food intake and body weight in a model of excessive eating. Metab Brain Dis. 2018;33(3):733-740.
Villa Pde S, Camargo GM, Camargo LA, Saad WA. Activation of paraventricular nucleus of hypothalamus 5-HT1A receptor on sodium intake. Regul Pept. 2007;140(3):142-147.
Polli FS, Gomes JN, Ferreira HS, Santana RC, Fregoneze JB. Inhibition of salt appetite in sodium-depleted rats by carvacrol: involvement of noradrenergic and serotonergic pathways. Eur J Pharmacol. 2019;854:119-127.
Takahashi M, Tanaka J. Serotonin release in the subfornical organ area induced by sodium and water intake in the rat. Physiol Behav. 2016;164:123-128.
Tanaka J, Hayashi Y, Yamato K, Miyakubo H, Nomura M. Involvement of serotonergic systems in the lateral parabrachial nucleus in sodium and water intake: a microdialysis study in the rat. Neurosci Lett. 2004;357(1):41-44.
de Magalhães-Nunes AP, Badauê-Passos D Jr, Ventura RR, et al. Sertraline, a selective serotonin reuptake inhibitor, affects thirst, salt appetite and plasma levels of oxytocin and vasopressin in rats. Exp Physiol. 2007;92(5):913-922.
Ferreyra MD, Chiaraviglio E. Changes in volemia and natremia and onset of sodium appetite in sodium depleted rats. Physiol Behav. 1977;19(2):197-201.
Wright M, Woodrow G, O'Brien S, et al. Disturbed appetite patterns and nutrient intake in peritoneal dialysis patients. Perit Dial Int. 2003;23(6):550-556.
Chung SH, Carrero JJ, Lindholm B. Causes of poor appetite in patients on peritoneal dialysis. J Ren Nutr. 2011;21(1):12-15.
Olivares EL, Costa-e-Sousa RH, Cavalcante-Lima HR, Lima HR, Cedraz-Mercez PL, Reis LC. Effect of electrolytic lesion of the dorsal raphe nucleus on water intake and sodium appetite. Braz J Med Biol Res. 2003;36:1709-1716.
Cavalcante-Lima HR, Badauê-Passos D Jr, de Lucca W Jr, et al. Chronic excitotoxic lesion of the dorsal raphe nucleus induces sodium appetite. Braz J Med Biol Res. 2005;38:1669-1675.
Tanaka J, Okumura T, Sakamaki K, Miyakubo H. Activation of serotonergic pathways from the midbrain raphe system to the subfornical organ by hemorrhage in the rat. Exp Neurol. 2001;169(1):156-162.
Franchini LF, Johnson AK, de Olmos J, Vivas L. Sodium appetite and Fos activation in serotonergic neurons. Am J Physiol Regul Integr Comp Physiol. 2002;282(1):R235-R243.
Mecawi AS, Vilhena-Franco T, Fonseca FV, Reis LS, Elias LL, Antunes-Rodrigues J. The role of angiotensin II on sodium appetite after a low-sodium diet. J Neuroendocrinol. 2013;25(3):281-291.
Porcari CY, Araujo IG, Urzedo-Rodrigues L, et al. Whole body sodium depletion modifies AT 1 mRNA expression and serotonin content in the dorsal raphe nucleus. J Neuroendocrinol. 2019;31(4):e12703.
Badauê-Passos D Jr, Godino A, Johnson AK, Vivas L, Antunes-Rodrigues J. Dorsal raphe nuclei integrate allostatic information evoked by depletion-induced sodium ingestion. Exp Neurol. 2007;206(1):86-94.
Gentili L, Saija A, Luchetti G, Massi M. Effect of the 5-HT2 antagonist ketanserin on salt appetite in the rat. Pharmacol Biochem Behav. 1991;39(1):171-176.
Castro L, Athanazio R, Barbetta M, et al. Central 5-HT2B/2C and 5-HT3 receptor stimulation decreases salt intake in sodium-depleted rats. Brain Res. 2003;981(1-2):151-159.
Fonseca FV, Mecawi AS, Araujo IG, et al. Role of the 5-HT1A somatodendritic autoreceptor in the dorsal raphe nucleus on salt satiety signaling in rats. Exp Neurol. 2009;217(2):353-360.
De Gobbi JI, Barbosa SP, De Luca LA Jr, Thunhorst RL, Johnson AK, Menani JV. Activation of serotonergic 5-HT1A receptors in the lateral parabrachial nucleus increases NaCl intake. Brain Res. 2005;1066(1-2):1-9.
Davern PJ, McKinley MJ. Forebrain regions affected by lateral parabrachial nucleus serotonergic mechanisms that influence sodium appetite. Brain Res. 2010;1339:41-48.
De Gobbi JI, De Luca LA Jr, Menani JV. Serotonergic mechanisms of the lateral parabrachial nucleus on DOCA-induced sodium intake. Brain Res. 2000;880(1-2):131-138.
David RB, Menani JV, De Luca LA Jr. Serotonergic receptor blockade in the lateral parabrachial nucleus: different effects on hypertonic and isotonic NaCl intake. Brain Res. 2008;1187:137-145.
Menani JV, Thunhorst RL, Johnson AK. Lateral parabrachial nucleus and serotonergic mechanisms in the control of salt appetite in rats. Am J Physiol Regul Integr Comp Physiol. 1996;270(1):R162-R168.
Menani JV, De Luca LA Jr, Johnson AK. Lateral parabrachial nucleus serotonergic mechanisms and salt appetite induced by sodium depletion. Am J Physiol Regul Integr Comp Physiol. 1998;274(2):R555-R560.
De Gobbi JI, Martinez G, Barbosa SP, et al. 5-HT2 and 5-HT3 receptors in the lateral parabrachial nucleus mediate opposite effects on sodium intake. Neuroscience. 2007;146(4):1453-1461.
Andrade-Franzé GM, Andrade CA, De Luca LA Jr, De Paula PM, Menani JV. Lateral parabrachial nucleus and central amygdala in the control of sodium intake. Neuroscience. 2010;165(3):633-641.
Park S, Williams KW, Liu C, Sohn JW. A neural basis for tonic suppression of sodium appetite. Nat Neurosci. 2020;23(3):423-432.
Luz C, Souza A, Reis R, et al. The central amygdala regulates sodium intake in sodium-depleted rats: role of 5-HT3 and 5-HT2C receptors. Brain Res. 2007;1139:178-194.
Luz C, Souza A, Reis R, Fregoneze JB, de Castro e Silva E. Role of 5-HT3 and 5-HT2C receptors located within the medial amygdala in the control of salt intake in sodium-depleted rats. Brain Res. 2006;1099(1):121-132.

Auteurs

Yurim Shin (Y)

Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, South Korea.

Seungjik Kim (S)

Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, South Korea.

Jong-Woo Sohn (JW)

Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, South Korea.

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