journal article Open Access Nov 18, 2015

Role of the clock gene Bmal1 and the gastric ghrelin-secreting cell in the circadian regulation of the ghrelin-GOAT system

View at Publisher Save 10.1038/srep16748
Abstract
AbstractAs adequate food intake is crucial to survival, organisms have evolved endogenous circadian clocks to generate optimal temporal patterns of food-related behavior and physiology. The gastric ghrelin-secreting cell is thought to be part of this network of peripheral food-entrainable oscillators (FEOs), regulating the circadian release of this orexigenic peptide. This study aimed to determine the role of the core clock gene Bmal1 and the gastric ghrelin-secreting cell as an FEO in the circadian rhythmicity of ghrelin expression and secretion in vivo and in vitro. Bmal1-deficient mice not only lacked circadian rhythmicity in plasma ghrelin levels and food intake, but also showed decreased gastric mRNA expression of ghrelin and ghrelin O-acyltransferase (GOAT), the ghrelin activating enzyme. Furthermore, in the absence of the hypothalamic master clock, food-related stimuli entrained the molecular clock of gastric ghrelinoma cells to regulate the rhythmic release of ghrelin. Divergent responses in octanoyl and total ghrelin release towards different food cues were observed, suggesting that the FEO also regulates the circadian rhythmicity of GOAT. Collectively, these findings indicate that circadian rhythmicity of ghrelin signaling requires Bmal1 and is driven by a food-responsive clock in the gastric ghrelin-secreting cell that not only regulates ghrelin, but also GOAT activity.
Topics

No keywords indexed for this article. Browse by subject →

References
56
[1]
Ghrelin is a growth-hormone-releasing acylated peptide from stomach

Masayasu Kojima, Hiroshi Hosoda, Yukari Date et al.

Nature 1999 10.1038/45230
[2]
Gutierrez, J. A. et al. Ghrelin octanoylation mediated by an orphan lipid transferase. Proc Natl Acad Sci USA 105(17), 6320–6325 (2008). 10.1073/pnas.0800708105
[3]
Identification of the Acyltransferase that Octanoylates Ghrelin, an Appetite-Stimulating Peptide Hormone

Jing Yang, Michael S. Brown, Guosheng Liang et al.

Cell 2008 10.1016/j.cell.2008.01.017
[4]
Patterson, M., Murphy, K. G., le Roux, C. W., Ghatei, M. A. & Bloom, S. R. Characterization of ghrelin-like immunoreactivity in human plasma. J Clin Endocrinol Metab 90 (4), 2205–2211 (2005). 10.1210/jc.2004-1641
[5]
Chen, H. Y. et al. Orexigenic action of peripheral ghrelin is mediated by neuropeptide Y and agouti-related protein. Endocrinology 145(6), 2607–2612 (2004). 10.1210/en.2003-1596
[6]
Avau, B., Carbone, F., Tack, J. & Depoortere, I. Ghrelin signaling in the gut, its physiological properties and therapeutic potential. Neurogastroenterol Motil 25(9), 720–732 (2013). 10.1111/nmo.12193
[7]
Muller, T. D. et al. Ghrelin. Molecular Metabolism 4(6), 437–460 (2015). 10.1016/j.molmet.2015.03.005
[8]
Asakawa, A. et al. Ghrelin is an appetite-stimulatory signal from stomach with structural resemblance to motilin. Gastroenterology 120(2), 337–345 (2001). 10.1053/gast.2001.22158
[9]
Tschop, M., Smiley, D. L. & Heiman, M. L. Ghrelin induces adiposity in rodents. Nature 407(6806), 908–913 (2000). 10.1038/35038090
[10]
Cummings, D. E. et al. A preprandial rise in plasma ghrelin levels suggests a role in meal initiation in humans. Diabetes 50(8), 1714–1719 (2001). 10.2337/diabetes.50.8.1714
[11]
Broglio, F. et al. Acetylcholine regulates ghrelin secretion in humans. J Clin Endocrinol Metab 89(5), 2429–2433 (2004). 10.1210/jc.2003-031517
[12]
Hosoda, H. & Kangawa, K. The autonomic nervous system regulates gastric ghrelin secretion in rats. Regul Pept 146(1–3), 12–18 (2008). 10.1016/j.regpep.2007.07.005
[13]
Mundinger, T. O., Cummings, D. E. & Taborsky, G. J., Jr. Direct stimulation of ghrelin secretion by sympathetic nerves. Endocrinology 147(6), 2893–2901 (2006). 10.1210/en.2005-1182
[14]
Callahan, H. S. et al. Postprandial suppression of plasma ghrelin level is proportional to ingested caloric load but does not predict intermeal interval in humans. J Clin Endocrinol Metab 89(3), 1319–1324 (2004). 10.1210/jc.2003-031267
[15]
Foster-Schubert, K. E. et al. Acyl and total ghrelin are suppressed strongly by ingested proteins, weakly by lipids and biphasically by carbohydrates. J Clin Endocrinol Metab 93(5), 1971–1979 (2008). 10.1210/jc.2007-2289
[16]
Depoortere, I. Taste receptors of the gut: emerging roles in health and disease. Gut 63(1), 179–190 (2014). 10.1136/gutjnl-2013-305112
[17]
Hass, N., Schwarzenbacher, K. & Breer, H. T1R3 is expressed in brush cells and ghrelin-producing cells of murine stomach. Cell Tissue Res 339(3), 493–504 (2010). 10.1007/s00441-009-0907-6
[18]
Janssen, S., Laermans, J., Iwakura, H., Tack, J. & Depoortere, I. Sensing of fatty acids for octanoylation of ghrelin involves a gustatory G-protein. PLoS One 7(6), e40168 (2012). 10.1371/journal.pone.0040168
[19]
Janssen, S. et al. Bitter taste receptors and alpha-gustducin regulate the secretion of ghrelin with functional effects on food intake and gastric emptying. Proc Natl Acad Sci USA 108(5), 2094–2099 (2011). 10.1073/pnas.1011508108
[20]
Bodosi, B. et al. Rhythms of ghrelin, leptin and sleep in rats: effects of the normal diurnal cycle, restricted feeding and sleep deprivation. Am J Physiol Regul Integr Comp Physiol 287(5), R1071–1079 (2004). 10.1152/ajpregu.00294.2004
[21]
Goel, N. et al. Circadian rhythm profiles in women with night eating syndrome. J Biol Rhythms 24(1), 85–94 (2009). 10.1177/0748730408328914
[22]
Shiiya, T. et al. Plasma ghrelin levels in lean and obese humans and the effect of glucose on ghrelin secretion. J Clin Endocrinol Metab 87(1), 240–244 (2002). 10.1210/jcem.87.1.8129
[23]
Yildiz, B. O., Suchard, M. A., Wong, M. L., McCann, S. M. & Licinio, J. Alterations in the dynamics of circulating ghrelin, adiponectin and leptin in human obesity. Proc Natl Acad Sci USA 101(28), 10434–10439 (2004). 10.1073/pnas.0403465101
[24]
Reppert, S. M. & Weaver, D. R. Coordination of circadian timing in mammals. Nature 418(6901), 935–941 (2002). 10.1038/nature00965
[25]
Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus

Francesca Damiola, Nguyet Le Minh, Nicolas Preitner et al.

Genes & Development 2000 10.1101/gad.183500
[26]
Entrainment of the Circadian Clock in the Liver by Feeding

Karl-Arne Stokkan, Shin Yamazaki, Hajime Tei et al.

Science 2001 10.1126/science.291.5503.490
[27]
Hara, R. et al. Restricted feeding entrains liver clock without participation of the suprachiasmatic nucleus. Genes Cells 6 (3), 269–278 (2001). 10.1046/j.1365-2443.2001.00419.x
[28]
Stomach ghrelin-secreting cells as food-entrainable circadian clocks

Joseph LeSauter, Nawshin Hoque, Michael Weintraub et al.

Proceedings of the National Academy of Sciences 2009 10.1073/pnas.0906426106
[29]
A Serum Shock Induces Circadian Gene Expression in Mammalian Tissue Culture Cells

Aurélio Balsalobre, Francesca Damiola, Ueli Schibler

Cell 1998 10.1016/s0092-8674(00)81199-x
[30]
Blum, I. D. et al. Reduced anticipatory locomotor responses to scheduled meals in ghrelin receptor deficient mice. Neuroscience 164 (2), 351–359 (2009). 10.1016/j.neuroscience.2009.08.009
[31]
Genomic Structure and Characterization of the 5′-Flanking Region of the Human Ghrelin Gene

Naotetsu Kanamoto, Takashi Akamizu, Tetsuya Tagami et al.

Endocrinology 2004 10.1210/en.2003-1718
[32]
Ariyasu, H. et al. Stomach is a major source of circulating ghrelin and feeding state determines plasma ghrelin-like immunoreactivity levels in humans. J Clin Endocrinol Metab 86(10), 4753–4758 (2001). 10.1210/jcem.86.10.7885
[33]
Dornonville de la Cour, C. et al. A-like cells in the rat stomach contain ghrelin and do not operate under gastrin control. Regul Pept 99(2-3), 141–150 (2001). 10.1016/s0167-0115(01)00243-9
[34]
Jeon, T. Y. et al. Changes in plasma ghrelin concentration immediately after gastrectomy in patients with early gastric cancer. J Clin Endocrinol Metab 89 (11), 5392–5396 (2004). 10.1210/jc.2004-0872
[35]
Bunger, M. K. et al. Mop3 is an essential component of the master circadian pacemaker in mammals. Cell 103(7), 1009–1017 (2000). 10.1016/s0092-8674(00)00205-1
[36]
Nakamura, T., Takumi, T., Takano, A., Hatanaka, F. & Yamamoto, Y. Characterization and modeling of intermittent locomotor dynamics in clock gene-deficient mice. PLoS One 8 (3), e58884 (2013). 10.1371/journal.pone.0058884
[37]
Hemmeryckx, B., Himmelreich, U., Hoylaerts, M. F. & Lijnen, H. R. Impact of clock gene Bmal1 deficiency on nutritionally induced obesity in mice. Obesity (Silver Spring) 19(3), 659–661 (2011). 10.1038/oby.2010.266
[38]
Hemmeryckx, B., Hoylaerts, M. F. & Lijnen, H. R. Effect of premature aging on murine adipose tissue. Exp Gerontol 47(3), 256–262 (2012). 10.1016/j.exger.2012.01.001
[39]
Lamia, K. A., Storch, K. F. & Weitz, C. J. Physiological significance of a peripheral tissue circadian clock. Proc Natl Acad Sci USA 105 (39), 15172–15177 (2008). 10.1073/pnas.0806717105
[40]
Turek, F. W. et al. Obesity and metabolic syndrome in circadian Clock mutant mice. Science 308(5724), 1043–1045 (2005). 10.1126/science.1108750
[41]
Shimba, S. et al. Brain and muscle Arnt-like protein-1 (BMAL1), a component of the molecular clock, regulates adipogenesis. Proc Natl Acad Sci USA 102 (34), 12071–12076 (2005). 10.1073/pnas.0502383102
[42]
Shimba, S. et al. Deficient of a clock gene, brain and muscle Arnt-like protein-1 (BMAL1), induces dyslipidemia and ectopic fat formation. PLoS One 6(9), e25231 (2011). 10.1371/journal.pone.0025231
[43]
Kennaway, D. J., Varcoe, T. J., Voultsios, A. & Boden, M. J. Global loss of bmal1 expression alters adipose tissue hormones, gene expression and glucose metabolism. PLoS One 8(6), e65255 (2013). 10.1371/journal.pone.0065255
[44]
Leliavski, A., Shostak, A., Husse, J. & Oster, H. Impaired glucocorticoid production and response to stress in Arntl-deficient male mice. Endocrinology 155(1), 133–142 (2013). 10.1210/en.2013-1531
[45]
De Boer, S. F. & Van der Gugten, J. Daily variations in plasma noradrenaline, adrenaline and corticosterone concentrations in rats. Physiol Behav 40(3), 323–328 (1987). 10.1016/0031-9384(87)90054-0
[46]
Durgan, D. J. et al. The intrinsic circadian clock within the cardiomyocyte. Am J Physiol Heart Circ Physiol 289(4), H1530–1541 (2005). 10.1152/ajpheart.00406.2005
[47]
Circadian Rhythms of Epinephrine and Norepinephrine in Man*

C. R. LINSELL, S. L. Lightman, P. E. MULLEN et al.

The Journal of Clinical Endocrinology & Metabo... 1985 10.1210/jcem-60-6-1210
[48]
Zhao, T. J. et al. Ghrelin secretion stimulated by {beta}1-adrenergic receptors in cultured ghrelinoma cells and in fasted mice. Proc Natl Acad Sci USA 107(36), 15868–15873 (2010). 10.1073/pnas.1011116107
[49]
Mendoza, J. Y., Aguilar-Roblero, R., Diaz-Munoz, M. & Escobar, C. Daily Epinephrine but not Norepinephrine Administration Produces Anticipatory Drinking Behavior in Rats. Biological Rhythm Research 34 (1), 73–90 (2003). 10.1076/brhm.34.1.73.14087
[50]
Terazono, H. et al. Adrenergic regulation of clock gene expression in mouse liver. Proc Natl Acad Sci USA 100(11), 6795–6800 (2003). 10.1073/pnas.0936797100

Showing 50 of 56 references

Cited By
53
Metrics
53
Citations
56
References
Details
Published
Nov 18, 2015
Vol/Issue
5(1)
License
View
Cite This Article
J. Laermans, L. Vancleef, J. Tack, et al. (2015). Role of the clock gene Bmal1 and the gastric ghrelin-secreting cell in the circadian regulation of the ghrelin-GOAT system. Scientific Reports, 5(1). https://doi.org/10.1038/srep16748