View Item 

Show simple item record

Ghrelin and cell differentiation

dc.contributor.authorXu, Geyangen_US
dc.contributor.authorLi, Yinen_US
dc.contributor.authorAn, Wenjiaoen_US
dc.contributor.authorZhang, Weizhenen_US
dc.date.accessioned2010-06-01T18:19:44Z
dc.date.available2010-06-01T18:19:44Z
dc.date.issued2008-10en_US
dc.identifier.citationXu, Geyang; Li, Yin; An, Wenjiao; Zhang, Weizhen (2008). "Ghrelin and cell differentiation." Acta Biochimica et Biophysica Sinica 40(10): 841-847. <http://hdl.handle.net/2027.42/71538>en_US
dc.identifier.issn1672-9145en_US
dc.identifier.issn1745-7270en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/71538
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=18850048&dopt=citationen_US
dc.format.extent241594 bytes
dc.format.extent3109 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Ltden_US
dc.rights© 2008 Institute of Biochemistry and Cell Biology, SIBS, CASen_US
dc.subject.otherGhrelinen_US
dc.subject.otherAdipogenesisen_US
dc.subject.otherMyogenesisen_US
dc.subject.otherOsteogenesisen_US
dc.subject.otherNeurogenesisen_US
dc.subject.otherPancreas Developmenten_US
dc.titleGhrelin and cell differentiationen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Surgery, University of Michigan Medical Center, Ann Arbor, Michigan 48109-0346, USAen_US
dc.contributor.affiliationotherDepartment of Physiology and Pathophysiology, Peking University Health Science Center, Beijing 100191, Chinaen_US
dc.identifier.pmid18850048en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/71538/1/j.1745-7270.2008.00465.x.pdf
dc.identifier.doi10.1111/j.1745-7270.2008.00465.xen_US
dc.identifier.sourceActa Biochimica et Biophysica Sinicaen_US
dc.identifier.citedreferenceKojima M, Hosoda H, Date Y, Nakazato M, Matsuo H, Kangawa K. Ghrelin is a growth-hormone-releasing acylated peptide from stomach. Nature 1999, 402: 656 – 660.en_US
dc.identifier.citedreferenceInui A, Asakawa A, Bowers CY, Mantovani G, Laviano A, Meguid MM, Fujimiya M. Ghrelin, appetite, and gastric motility: the emerging role of the stomach as an endocrine organ. FASEB J 2004, 18: 439 – 456.en_US
dc.identifier.citedreferenceTorsello A, Scibona B, Leo G, Bresciani E, Avallone R, Bulgarelli I, Luoni M et al. Ontogeny and tissue-specific regulation of ghrelin mRNA expression suggest that ghrelin is primarily involved in the control of extraendocrine functions in the rat. Neuroendocrinol-ogy 2003, 77: 91 – 99.en_US
dc.identifier.citedreferenceMiao Y, Xia Q, Hou ZS, Zheng Y, Pan H, Zhu SG. Ghrelin protects cortical neuron against focal ischemia/reperfusion in rats. Biochem Biophys Res Commun 2007, 359: 795 – 800.en_US
dc.identifier.citedreferenceKamegai J, Tamura H, Shimizu T, Ishii S, Sugihara H, Oikawa S. Regulation of the ghrelin gene: growth hormone-releasing hormone upregulates ghrelin mRNA in the pituitary. Endocrinology 2001, 142: 4154 – 4157.en_US
dc.identifier.citedreferenceWierup N, Yang S, McEvilly RJ, Mulder H, Sundler F. Ghrelin is expressed in a novel endocrine cell type in developing rat islets and inhibits insulin secretion from INS-1 (832/13) cells. J Histochem Cytochem 2004, 52: 301 – 310.en_US
dc.identifier.citedreferenceSusiec H, Maria G, Marta K. Ghrelin: the peripheral hunger hormone. Trends Mol Med 2007, 39: 116 – 136.en_US
dc.identifier.citedreferenceTakaya K, Ariyasu H, Kanamoto N, Iwakura H, Yoshimoto A, Harada M, Mori K et al. Ghrelin strongly stimulates growth hormone release in humans. J Clin Endocrinol Metab 2000, 85: 4908 – 4911.en_US
dc.identifier.citedreferenceWren AM, Small CJ, Ward HL, Murphy KG, Dakin CL, Taheri S, Kennedy AR et al. The novel hypothalamic peptide ghrelin stimulates food intake and growth hormone secretion. Endocrinology 2000, 141: 4325 – 4328.en_US
dc.identifier.citedreferenceCamifla JP, Carreira MC, Micic D, Pombo M, Kelestimur F, Dieguez C, Casanueva FF. Regulation of ghrelin secretion and action. Endocrine 2003, 22: 5 – 12.en_US
dc.identifier.citedreferenceKojima M, Kangawa K. Ghrelin: structure and function. Physiol Rev 2005, 85: 495 – 522.en_US
dc.identifier.citedreferenceZhang M, Yuan F, Chen H, Qiu XB, Fang WY Effect of exogenous ghrelin on cell differentiation antigen 40 expression in endothelial cells. Acta Biochim Biophys Sin 2007, 39: 974 – 998.en_US
dc.identifier.citedreferenceDixit DV, Schaffer EM, Pyle R, Collins GD, Sakthivel SK, Palaniappan R, Lillard JW et al. Ghrelin inhibits leptin- and activation-induced proinflammatory cytokine expression by human mono-cytes and T cells. J Clin Invest 2004, 114: 57 – 66.en_US
dc.identifier.citedreferenceWang ZG, Wang WG, Qiu WC, Fan YB, Zhao J, Wang Y, Zhang Q. Involvement of ghrelin-growth hormone secretagogue receptor system in pathoclinical profiles of digestive system cancer. Acta Biochim Biophys Sin 2007, 39: 992 – 998.en_US
dc.identifier.citedreferenceBarreiro ML, Tena-Sempere M. Ghrelin and reproduction: a novel signal linking energy status and fertility ? Mol Cell Endocrinol 2004, 226: 1 – 9.en_US
dc.identifier.citedreferenceChanoine JP, Wong AC. Ghrelin gene expression is markedly higher in fetal pancreas compared with fetal stomach: effect of maternal fasting. Endocrinology 2004, 145: 3813 – 3820.en_US
dc.identifier.citedreferenceCortelazzi D, Cappiello V, Morpurgo PS, Ronzoni S, Nobile De Santis MS, Cetin I, Beck-Peccoz P et al. Circulating levels of ghrelin in human fetuses. Eur J Endocrinol 2003, 149: 111 – 116.en_US
dc.identifier.citedreferenceMakino Y, Hosoda H, Shibata K, Makino I, Kojima M, Kangawa K, Kawarabayashi T. Alteration of plasma ghrelin levels associated with the blood pressure in pregnancy. Hypertension 2002, 39: 781 – 784.en_US
dc.identifier.citedreferenceTorsello A, Scibona B, Leo G, Bresciani E, Avallone R, Bulgarelli I, Luoni M et al. Ontogeny and tissue-specific regulation of ghrelin mRNA expression suggest that ghrelin is primarily involved in the control of extraendocrine functions in the rat. Neuroendocrinol-ogy 2003, 77: 91 – 99.en_US
dc.identifier.citedreferenceLiu YL, Yakar S, Otero-Corchon V, Low MJ, Liu JL. Ghrelin gene expression is age-dependent and influenced by gender and the level of circulating IGF-I. Mol Cell Endocrinol 2002, 189: 97 – 103.en_US
dc.identifier.citedreferencePrado CL, Pugh-Bernard AE, Elghazi L, Sosa-Pineda B, Sussel L. Ghrelin cells replace insulin-producing Β cells in two mouse models of pancreas development. Proc Natl Acad Sci USA 2004, 101: 2924 – 2929.en_US
dc.identifier.citedreferenceHayashida T, Nakahara K, Mondal MS, Date Y, Nakazato M, Kojima M, Kangawa K et al. Ghrelin in neonatal rats: distribution in stomach and its possible role. J Endocrinol 2002, 173: 239 – 245.en_US
dc.identifier.citedreferenceIrako T, Akamizu T, Hosoda H, Iwakura H, Ariyasu H, Tojo K, Tajima N et al. Ghrelin prevents development of diabetes at adult age in streptozotocin-treated newborn rats. Diabetologia 2006, 49: 1264 – 1273.en_US
dc.identifier.citedreferenceKim SW, Her SJ, Park SJ, Kim S, Park KS, Lee HK, Han BH et al. Ghrelin stimulates proliferation and differentiation and inhibits apoptosis in osteoblastic MC3T3-E1 cells. Bone 2005, 37: 59 – 69.en_US
dc.identifier.citedreferenceMaccarinelli G, Sibilia V, Torsello A, Raimondo F, Pitto M, Giustina A, Netti C et al. Ghrelin regulates proliferation and differentiation of osteoblastic cells. J Endocrinol 2005, 184: 249 – 256.en_US
dc.identifier.citedreferenceZhang W, Lin TR, Hu Y, Fan Y, Zhao L, Stuenkel EL, Mulholland MW. Ghrelin stimulates neurogenesis in the dorsal motor nucleus of the vagus. J Physiol 2004, 559: 729 – 737.en_US
dc.identifier.citedreferenceSato M, Nakahara K, Goto S, Kaiya H, Miyazato M, Date Y, Nakazato M et al. Effects of ghrelin and des-acyl ghrelin on neurogenesis of the rat fetal spinal cord. Biochem Biophys Res Commun 2006, 350: 598 – 603.en_US
dc.identifier.citedreferenceZhang W, Zhao L, Lin TR, Chai B, Fan Y, Gantz I, Mulholland MW. Inhibition of adipogenesis by ghrelin. Mol Biol Cell 2004, 15: 2484 – 2491.en_US
dc.identifier.citedreferenceKim MS, Yoon CY, Jang PG, Park YJ, Shin CS, Park HS, Ryu JW et al. The mitogenic and antiapoptotic actions of ghrelin in 3T3-L1 adipocytes. Mol Endocrinol 2004, 18: 2291 – 2301.en_US
dc.identifier.citedreferencePettersson I, Muccioli G, Granata R, Deghenghi R, Ghigo E, Ohlsson C, Isgaard J. Natural (ghrelin) and synthetic (hexarelin) GH secreta-gogues stimulate H9c2 cardiomyocyte cell proliferation. J Endocrinol 2002, 175: 201 – 209.en_US
dc.identifier.citedreferenceNanzer AM, Khalaf S, Mozid AM, Fowkes RC, Patel MV, Burrin JM, Grossman AB et al. Ghrelin exerts a proliferative effect on a rat pituitary somatotroph cell line via the mitogen activated protein kinase pathway. Eur J Endocrinol 2004, 151: 233 – 240.en_US
dc.identifier.citedreferenceCassoni P, Ghe C, Marrocco T, Tarabra E, Allia E, Catapano F, Deghenghi R et al. Expression of ghrelin and biological activity of specific receptors for ghrelin and des-acyl ghrelin in human prostate neoplasms and related cell lines. Eur J Endocrinol 2004, 150: 173 – 184.en_US
dc.identifier.citedreferenceVolante M, Allia E, Fulcheri E, Cassoni P, Ghigo E, Muccioli G, Papotti M. Ghrelin in fetal thyroid and follicular tumors and cell. lines: expression and effects on tumor growth. Am J Pathol 2003, 162: 645 – 654.en_US
dc.identifier.citedreferenceCassoni P, Papotti M, Ghe C, Catapano F, Sapino A, Graziani A, Deghenghi R et al. Identification, characterization, and biological activity of specific receptors for natural (ghrelin) and synthetic growth hormone secretagogues and analogs in human breast carcinomas and cell lines. J Clin Endocrinol Metab 2001, 86: 1738 – 1745.en_US
dc.identifier.citedreferenceGhe C, Cassoni P, Catapano F, Marrocco T, Deghenghi R, Ghigo E, Muccioli G et al. The antiproliferative effect of synthetic peptidyl GH secretagogues in human CALU-1 lung carcinoma cells. Endocrinology 2002, 143: 484 – 491.en_US
dc.identifier.citedreferenceTschop M, Smiley DL, Heiman ML. Ghrelin induces adiposity in rodents. Nature 2000, 407: 908 – 913.en_US
dc.identifier.citedreferenceChoi K, Roh SG, Hong YH, Shrestha YB, Hishikawa D, Chen C, Kojima M et al. The role of ghrelin and growth hormone secretagogues receptor on rat adipogenesis. Endocrinology 2003, 144: 754 – 759.en_US
dc.identifier.citedreferenceOtt V, Fasshauer M, Dalski A, Meier B, Perwitz N, Klein H, Tschop M et al. Direct peripheral effects of ghrelin include suppression of adiponectin expression. Horm Metab Res 2002, 34: 640 – 645.en_US
dc.identifier.citedreferenceThompson N, Gill D, Davies R, Loveridge N, Houston P, Robinson I. Wells T. Ghrelin and des-octanoyl ghrelin promote adipogenesis directly in vivo by a mechanism independent of the type la growth hormone secretagogue receptor. Endocrinology 2004, 145: 234 – 242.en_US
dc.identifier.citedreferenceHu E, Kim JB, Sarraf P, Spiegelman BM. Inhibition of adipogenesis through MAP kinase-mediated phosphorylation of PPAR gamma. Science 1996, 274: 2100 – 2103.en_US
dc.identifier.citedreferenceLongo KA, Wright WS, Kang S, Gerin I, Chiang SH, Lucas PC, Opp MR et al. Wnt10b inhibits development of white and brown adipose tissues. J Biol Chem 2004, 279: 35503 – 35509.en_US
dc.identifier.citedreferenceZhang W, Chai B, Li J, Wang H, Mulholland MW. Effect of des-acyl ghrelin on adiposity and glucose metabolism. Endocrinology 2008, 149: 4710 – 4716.en_US
dc.identifier.citedreferenceZhang W, Zhao L, Mulholland MW. Ghrelin stimulates myocyte development. Cell Physiol Biochem 2007, 20: 659 – 664.en_US
dc.identifier.citedreferenceFiligheddu N, Gnocchi VF, Coscia M, Cappelli M, Porporato PE, Taulli R, Traini S et al. Ghrelin and des-acyl ghrelin promote differentiation and fusion of C2C12 skeletal muscle cells. Mol Biol Cell 2007, 18: 986 – 994.en_US
dc.identifier.citedreferenceFukushima N, Hanada R, Teranishi H, Fukue Y, Tachibana T, Ishikawa H, Takeda S et al. Ghrelin directly regulates bone formation. J Bone Miner Res 2005, 20: 790 – 798.en_US
dc.identifier.citedreferenceMisra M, Miller K, Stewart V, Hunter E, Kuo K, Herzog D, Klibanski A. Ghrelin and bone metabolism in adolescent girls with anorexia nervosa and healthy adolescents. J Clin Endocrinol Metab 2005, 90: 5082 – 5087.en_US
dc.identifier.citedreferenceDeng FL, Ling JQ, Ma JY, Liu CH, Zhang W. Stimulation of in-tramembranous bone repair by ghrelin. Exp Physiol 2008, 937: 872 – 879.en_US
dc.identifier.citedreferenceDelhanty PJ, Eerden BC, Velde M, Gauna C, Pols HA, Jahr H, Chiba H et al. Ghrelin and unacylated ghrelin stimulate human osteoblast growth via mitogen-activated protein kinase (MAPK)/phosphoinositide 3-kinase (PI3K) pathways in the absence of GHSR-la. J Endocrinol 2006, 188: 37 – 47.en_US
dc.identifier.citedreferenceAlvarez BA, Garcia-Verdugo JM. Neurogenesis in adult subventricular zone. J Neurosci 2002, 22: 629 – 634.en_US
dc.identifier.citedreferenceJin K, Mao XO, Sun Y, Xie L, Greenberg DA. Stem cell factor stimulates neurogenesis in vitro and in vivo. J Clin Invest 2002, 110: 311 – 319.en_US
dc.identifier.citedreferenceGross PM, Wall KM, Pang JJ, Shaver SW, Wainman DS. Microvas-cular specializations promoting rapid interstitial solute dispersion in nucleus tractus solitarius. Am J Physiol 1990 259: 1131 – 1138.en_US
dc.identifier.citedreferenceHermann GE, Emch GS, Tovar CA, Rogers RC. c-fos generation in the dorsal vagal complex after systemic endotoxin is not dependent on the vagus-nerve. Am J Physiol 2001, 280: 289 – 299.en_US
dc.identifier.citedreferenceMachaalani R, Waters KA. Increased neuronal cell death after intermittent hypercapnic hypoxia in the developing piglet brainstem. Brain Res 2003, 985: 127 – 134.en_US
dc.identifier.citedreferenceYuan PQ, Yang H. Neuronal activation of brain vagal-regulatory pathways and upper gut enteric plexuses by insulin hypoglycemia. Am J Physiol Endocrinol Metab 2002, 283: 436 – 448.en_US
dc.identifier.citedreferenceZhang W, Hu Y, Lin TR, Fan Y, Mulholland MW. Stimulation of neurogenesis in rat nucleus of the solitary tract by ghrelin. Peptides 2005, 26: 2280 – 2288.en_US
dc.identifier.citedreferenceSato M, Nakahara K, Goto S, Kaiya H, Miyazato M, Date Y, Nakazato M et al. Effects of ghrelin and des-acyl ghrelin on neurogenesis of the rat fetal spinal cord. Biochem Biophys Res Commun 2006, 350: 598 – 603.en_US
dc.identifier.citedreferenceMiao Y, Xia Q, Hou Z, Zheng Y, Pan H, Zhu S. Ghrelin protects cortical neuron against focal ischemia/reperfusion in rats. Biochem Biophys Res Commun 2007, 359: 795 – 800.en_US
dc.identifier.citedreferenceChung H, Kim E, Lee D, Seo S, Ju S, Lee D, Kim H et al. Ghrelin inhibits apoptosis in hypothalamic neuronal cells during oxygen-glucose deprivation. Endocrinology 2007, 148: 148 – 159.en_US
dc.identifier.citedreferenceChung H, Seo S, Moon M, Park S. Phosphatidylinositol-3-kinase/Akt/glycogen synthase kinase-3Β and ERK1/2 pathways mediate protective effects of acylated and unacylated ghrelin against oxygen-glucose deprivation-induced apoptosis in primary rat cortical neuronal cells. J Endocrinol 2008, 198: 511 – 521.en_US
dc.identifier.citedreferenceLaiwand R, Werman R, Yarom Y. Time course and distribution of motoneuronal loss in the dorsal motor vagal nucleus of guinea pig after cervical vagotomy. J Comp Neurol 1987, 256: 527 – 537.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Name:
j.1745-7270.2008.00465.x.pdf
Size:
235.9KB
Format:
PDF
View/Open

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.