FGF21: Difference between revisions

Jump to navigation Jump to search
VisualWikitext
(#REDIRECT [[<span dir="auto">Fibroblast growth factor</span>]])
 
m (Reverted 1 edit by 1.36.149.81 (talk) to last revision by KolbertBot. (TW))
Line 1: Line 1:
#REDIRECT [[Fibroblast growth factor]]
{{Infobox_gene}}
'''Fibroblast growth factor 21''' is a [[protein]] that in mammals is encoded by the ''FGF21'' [[gene]].<ref name="pmid10858549">{{cite journal | vauthors = Nishimura T, Nakatake Y, Konishi M, Itoh N | title = Identification of a novel FGF, FGF-21, preferentially expressed in the liver | journal = Biochimica et Biophysica Acta | volume = 1492 | issue = 1 | pages = 203–6 | date = Jun 2000 | pmid = 10858549 | pmc =  | doi = 10.1016/S0167-4781(00)00067-1 }}</ref><ref name="pmid10858549" /><ref name="entrez_ 26291">{{cite web | title = Entrez Gene: FGF21 fibroblast growth factor 21| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=26291| accessdate = }}</ref> The [[protein]] encoded by this gene is a member of the [[fibroblast growth factor]] (FGF) family and specifically a member of the endocrine subfamily which includes FGF23 and FGF15/19.
 
FGF family members possess broad mitogenic and cell survival activities and are involved in a variety of biological processes including [[Embryogenesis|embryonic development]], cell growth, [[morphogenesis]], tissue repair, tumor growth and invasion.<ref name="entrez_ 26291"/> FGFs act through a family of four FGF receptors. Binding is complicated and requires both interaction of the FGF molecule with an FGF receptor and binding to heparin through an heparin binding domain. Endocrine FGFs lack a heparin binding domain and thus can be released into the circulation. FGF21 action through one of the FGF21 receptors thus requires interaction with a co-receptor, designated [[β-klotho]].
 
==Regulation==
 
FGF21 is specifically induced by [[HMGCS2 (gene)|HMGCS2]] activity. The oxidized form of ketone bodies (acetoacetate) in a cultured medium also induced FGF21, possibly via a [[SIRT1]]-dependent mechanism.<ref>{{cite journal | vauthors = Vilà-Brau A, De Sousa-Coelho AL, Mayordomo C, Haro D, Marrero PF | title = Human HMGCS2 regulates mitochondrial fatty acid oxidation and FGF21 expression in HepG2 cell line | journal = The Journal of Biological Chemistry | volume = 286 | issue = 23 | pages = 20423–30 | date = Jun 2011 | pmid = 21502324 | pmc = 3121469 | doi = 10.1074/jbc.M111.235044 }}</ref> HMGCS2 activity has also been shown to be increased by deacetylation of lysines 310, 447, and 473 via [[SIRT3]] in the mitochondria.<ref>{{cite journal | vauthors = Shimazu T, Hirschey MD, Hua L, Dittenhafer-Reed KE, Schwer B, Lombard DB, Li Y, Bunkenborg J, Alt FW, Denu JM, Jacobson MP, Verdin E | title = SIRT3 deacetylates mitochondrial 3-hydroxy-3-methylglutaryl CoA synthase 2 and regulates ketone body production | journal = Cell Metabolism | volume = 12 | issue = 6 | pages = 654–61 | date = Dec 2010 | pmid = 21109197 | pmc = 3310379 | doi = 10.1016/j.cmet.2010.11.003 }}</ref>
 
While FGF21 is expressed in numerous tissues, including liver, [[brown adipose tissue]], [[white adipose tissue]] and pancreas, circulating levels of FGF21 are derived specifically from the liver in mice.<ref>{{cite journal | vauthors = Markan KR, Naber MC, Ameka MK, Anderegg MD, Mangelsdorf DJ, Kliewer SA, Mohammadi M, Potthoff MJ | title = Circulating FGF21 is liver derived and enhances glucose uptake during refeeding and overfeeding | journal = Diabetes | volume = 63 | issue = 12 | pages = 4057–63 | date = Dec 2014 | pmid = 25008183 | pmc = 4238010 | doi = 10.2337/db14-0595 }}</ref> In liver FGF21 expression is regulated by PPARα and levels rise substantially with both fasting and consumption of ketogenic diets.
 
[[Liver X receptor|LXR]] represses FGF21 in humans via an LXR response element located from -37 to -22 bp on the human FGF21 promoter.<ref>{{cite journal | vauthors = Uebanso T, Taketani Y, Yamamoto H, Amo K, Tanaka S, Arai H, Takei Y, Masuda M, Yamanaka-Okumura H, Takeda E | title = Liver X receptor negatively regulates fibroblast growth factor 21 in the fatty liver induced by cholesterol-enriched diet | journal = The Journal of Nutritional Biochemistry | volume = 23 | issue = 7 | pages = 785–90 | date = Jul 2012 | pmid = 21889884 | doi = 10.1016/j.jnutbio.2011.03.023 }}</ref>
 
== Function ==
 
FGF21 stimulates [[glucose]] uptake in [[adipocyte]]s but not in other cell types.<ref name="pmid15902306">{{cite journal | vauthors = Kharitonenkov A, Shiyanova TL, Koester A, Ford AM, Micanovic R, Galbreath EJ, Sandusky GE, Hammond LJ, Moyers JS, Owens RA, Gromada J, Brozinick JT, Hawkins ED, Wroblewski VJ, Li DS, Mehrbod F, Jaskunas SR, Shanafelt AB | title = FGF-21 as a novel metabolic regulator | journal = The Journal of Clinical Investigation | volume = 115 | issue = 6 | pages = 1627–35 | date = Jun 2005 | pmid = 15902306 | pmc = 1088017 | doi = 10.1172/JCI23606 }}</ref> This effect is additive to the activity of [[insulin]]. FGF21 treatment of adipocytes is associated with [[phosphorylation]] of [[FRS2]], a protein linking FGF receptors to the [[MAPK/ERK pathway|Ras/MAP kinase pathway]]. FGF21 injection in [[ob/ob mice]] results in an increase in [[Glut1]] in [[adipose]] tissue. FGF21 also protects animals from diet-induced [[obesity]] when overexpressed in [[transgenic]] mice  and lowers blood glucose and [[triglyceride]] levels when administered to [[diabetes mellitus|diabetic]] rodents.<ref name="pmid15902306"/> Treatment of animals with FGF21 results in increased energy expenditure, fat utilization and lipid excretion.<ref name="pmid18687777">{{cite journal | vauthors = Coskun T, Bina HA, Schneider MA, Dunbar JD, Hu CC, Chen Y, Moller DE, Kharitonenkov A | title = Fibroblast growth factor 21 corrects obesity in mice | journal = Endocrinology | volume = 149 | issue = 12 | pages = 6018–27 | date = Dec 2008 | pmid = 18687777 | doi = 10.1210/en.2008-0816 }}</ref>
 
Beta Klotho ({{gene|KLB}}) functions as a cofactor essential for FGF21 activity.<ref name="pmid17452648">{{cite journal | vauthors = Ogawa Y, Kurosu H, Yamamoto M, Nandi A, Rosenblatt KP, Goetz R, Eliseenkova AV, Mohammadi M, Kuro-o M | title = BetaKlotho is required for metabolic activity of fibroblast growth factor 21 | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 104 | issue = 18 | pages = 7432–7 | date = May 2007 | pmid = 17452648 | pmc = 1855074 | doi = 10.1073/pnas.0701600104 | bibcode = 2007PNAS..104.7432O }}</ref>
 
In cows plasma FGF21 was nearly undetectable in late pregnancy (LP), peaked at parturition, and then stabilized at lower, chronically elevated concentrations during early lactation (EL). Plasma FGF21 was similarly increased in the absence of parturition when an energy-deficit state was induced by feed restricting late-lactating dairy cows, implicating energy insufficiency as a cause of chronically elevated FGF21 in EL. The liver was the major source of plasma FGF21 in early lactation with little or no contribution by [[white adipose tissue|WAT]], skeletal muscle, and mammary gland. Meaningful expression of the FGF21 coreceptor β-Klotho was restricted to liver and WAT in a survey of 15 tissues that included the mammary gland. Expression of β-Klotho and its subset of interacting FGF receptors was modestly affected by the transition from LP to EL in liver but not in WAT.<ref>{{cite journal | vauthors = Schoenberg KM, Giesy SL, Harvatine KJ, Waldron MR, Cheng C, Kharitonenkov A, Boisclair YR | title = Plasma FGF21 is elevated by the intense lipid mobilization of lactation | journal = Endocrinology | volume = 152 | issue = 12 | pages = 4652–61 | date = Dec 2011 | pmid = 21990311 | doi = 10.1210/en.2011-1425 }}</ref>
 
==Clinical significance==
 
Serum FGF-21 levels were significantly increased in patients with  [[type 2 diabetes mellitus]] (T2DM) which may indicate a role in the pathogenesis of T2DM.<ref>{{cite journal | vauthors = Cheng X, Zhu B, Jiang F, Fan H | title = Serum FGF-21 levels in type 2 diabetic patients | journal = Endocrine Research | volume = 36 | issue = 4 | pages = 142–8 | year = 2011 | pmid = 21973233 | doi = 10.3109/07435800.2011.558550 }}</ref> Elevated levels also correlate with liver fat content in non-alcoholic fatty liver disease<ref>{{cite journal | vauthors = Yan H, Xia M, Chang X, Xu Q, Bian H, Zeng M, Rao S, Yao X, Tu Y, Jia W, Gao X | title = Circulating fibroblast growth factor 21 levels are closely associated with hepatic fat content: a cross-sectional study | journal = PLOS ONE | volume = 6 | issue = 9 | pages = e24895 | year = 2011 | pmid = 21949781 | pmc = 3174975 | doi = 10.1371/journal.pone.0024895 | bibcode = 2011PLoSO...624895Y }}</ref> and positively correlate with BMI in humans suggesting obesity as a FGF21-resistant state.<ref>{{cite journal | vauthors = Kralisch S, Fasshauer M | title = Fibroblast growth factor 21: effects on carbohydrate and lipid metabolism in health and disease | journal = Current Opinion in Clinical Nutrition and Metabolic Care | volume = 14 | issue = 4 | pages = 354–9 | date = Jul 2011 | pmid = 21505329 | doi = 10.1097/MCO.0b013e328346a326 }}</ref>
 
==Animal studies==
Mice lacking FGF21 fail to fully induce [[PPARGC1A|PGC-1α]] expression in response to a prolonged fast and have impaired gluconeogenesis and ketogenesis.<ref>{{cite journal | vauthors = Potthoff MJ, Inagaki T, Satapati S, Ding X, He T, Goetz R, Mohammadi M, Finck BN, Mangelsdorf DJ, Kliewer SA, Burgess SC | title = FGF21 induces PGC-1alpha and regulates carbohydrate and fatty acid metabolism during the adaptive starvation response | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 106 | issue = 26 | pages = 10853–8 | date = Jun 2009 | pmid = 19541642 | pmc = 2705613 | doi = 10.1073/pnas.0904187106 | bibcode = 2009PNAS..10610853P }}</ref>
 
FGF21 stimulates phosphorylation of fibroblast growth factor receptor substrate 2 and [[Extracellular signal-regulated kinases|ERK1/2]] in the liver. Acute FGF21 treatment induced hepatic expression of key regulators of gluconeogenesis, lipid metabolism, and ketogenesis including glucose-6-phosphatase, phosphoenol pyruvate carboxykinase, 3-hydroxybutyrate dehydrogenase type 1, and carnitine palmitoyltransferase 1α. In addition, injection of FGF21 was associated with decreased circulating [[insulin]] and free fatty acid levels. FGF21 treatment induced mRNA and protein expression of PGC-1α, but in mice PGC-1α expression was not necessary for the effect of FGF21 on glucose metabolism.<ref>{{cite journal | vauthors = Fisher FM, Estall JL, Adams AC, Antonellis PJ, Bina HA, Flier JS, Kharitonenkov A, Spiegelman BM, Maratos-Flier E | title = Integrated regulation of hepatic metabolism by fibroblast growth factor 21 (FGF21) in vivo | journal = Endocrinology | volume = 152 | issue = 8 | pages = 2996–3004 | date = Aug 2011 | pmid = 21712364 | pmc = 3138239 | doi = 10.1210/en.2011-0281 }}</ref>
 
In mice FGF21 is strongly induced in liver by prolonged fasting via [[Peroxisome proliferator-activated receptor alpha|PPAR-alpha]] and in turn induces the transcriptional coactivator PGC-1α and stimulates hepatic gluconeogenesis, fatty acid oxidation, and ketogenesis. FGF21 also blocks somatic growth and sensitizes mice to a hibernation-like state of torpor, playing a key role in eliciting and coordinating the adaptive starvation response. FGF21 expression is also induced in white adipose tissue by [[Peroxisome proliferator-activated receptor gamma|PPAR-gamma]], which may indicate it also regulates metabolism in the fed state.<ref>{{cite journal | vauthors = Kliewer SA, Mangelsdorf DJ | title = Fibroblast growth factor 21: from pharmacology to physiology | journal = The American Journal of Clinical Nutrition | volume = 91 | issue = 1 | pages = 254S–257S | date = Jan 2010 | pmid = 19906798 | pmc = 2793111 | doi = 10.3945/ajcn.2009.28449B }}</ref>
 
Activation of [[AMP-activated protein kinase|AMPK]] and SIRT1 by FGF21 in adipocytes enhanced mitochondrial oxidative capacity as demonstrated by increases in oxygen consumption, citrate synthase activity, and induction of key metabolic genes. The effects of FGF21 on mitochondrial function require serine/threonine kinase 11 (STK11/LKB1), which activates AMPK. Inhibition of AMPK, SIRT1, and PGC-1α activities attenuated the effects of FGF21 on oxygen consumption and gene expression, indicating that FGF21 regulates mitochondrial activity and enhances oxidative capacity through an LKB1-AMPK-SIRT1-PGC-1α-dependent mechanism in adipocytes, resulting in increased phosphorylation of AMPK, increased cellular NAD+ levels and activation of SIRT1 and deacetylation of SIRT1 targets PGC-1α and [[histone 3]].<ref>{{cite journal | vauthors = Chau MD, Gao J, Yang Q, Wu Z, Gromada J | title = Fibroblast growth factor 21 regulates energy metabolism by activating the AMPK-SIRT1-PGC-1alpha pathway | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 107 | issue = 28 | pages = 12553–8 | date = Jul 2010 | pmid = 20616029 | pmc = 2906565 | doi = 10.1073/pnas.1006962107 | bibcode = 2010PNAS..10712553C }}</ref>
 
Acutely, the rise in FGF21 in response to alcohol consumption inhibits further drinking. Chronically, the rise in FGF21 expression in the liver may protect against liver damage.
 
== References ==
{{Reflist|2}}
 
== Further reading ==
{{refbegin | 2}}
* {{cite journal | vauthors = Chen WW, Li L, Yang GY, Li K, Qi XY, Zhu W, Tang Y, Liu H, Boden G | title = Circulating FGF-21 levels in normal subjects and in newly diagnose patients with Type 2 diabetes mellitus | journal = Experimental and Clinical Endocrinology & Diabetes | volume = 116 | issue = 1 | pages = 65–8 | date = Jan 2008 | pmid = 17926232 | doi = 10.1055/s-2007-985148 }}
* {{cite journal | vauthors = Ogawa Y, Kurosu H, Yamamoto M, Nandi A, Rosenblatt KP, Goetz R, Eliseenkova AV, Mohammadi M, Kuro-o M | title = BetaKlotho is required for metabolic activity of fibroblast growth factor 21 | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 104 | issue = 18 | pages = 7432–7 | date = May 2007 | pmid = 17452648 | pmc = 1855074 | doi = 10.1073/pnas.0701600104 | bibcode = 2007PNAS..104.7432O }}
* {{cite journal | vauthors = Kharitonenkov A, Wroblewski VJ, Koester A, Chen YF, Clutinger CK, Tigno XT, Hansen BC, Shanafelt AB, Etgen GJ | title = The metabolic state of diabetic monkeys is regulated by fibroblast growth factor-21 | journal = Endocrinology | volume = 148 | issue = 2 | pages = 774–81 | date = Feb 2007 | pmid = 17068132 | doi = 10.1210/en.2006-1168 }}
* {{cite journal | vauthors = Kharitonenkov A, Shiyanova TL, Koester A, Ford AM, Micanovic R, Galbreath EJ, Sandusky GE, Hammond LJ, Moyers JS, Owens RA, Gromada J, Brozinick JT, Hawkins ED, Wroblewski VJ, Li DS, Mehrbod F, Jaskunas SR, Shanafelt AB | title = FGF-21 as a novel metabolic regulator | journal = The Journal of Clinical Investigation | volume = 115 | issue = 6 | pages = 1627–35 | date = Jun 2005 | pmid = 15902306 | pmc = 1088017 | doi = 10.1172/JCI23606 }}
* {{cite journal | vauthors = Zhang Z, Henzel WJ | title = Signal peptide prediction based on analysis of experimentally verified cleavage sites | journal = Protein Science | volume = 13 | issue = 10 | pages = 2819–24 | date = Oct 2004 | pmid = 15340161 | pmc = 2286551 | doi = 10.1110/ps.04682504 }}
* {{cite journal | vauthors = Popovici C, Conchonaud F, Birnbaum D, Roubin R | title = Functional phylogeny relates LET-756 to fibroblast growth factor 9 | journal = The Journal of Biological Chemistry | volume = 279 | issue = 38 | pages = 40146–52 | date = Sep 2004 | pmid = 15199049 | doi = 10.1074/jbc.M405795200 }}
* {{cite journal | vauthors = Popovici C, Conchonaud F, Birnbaum D, Roubin R | title = Functional phylogeny relates LET-756 to fibroblast growth factor 9 | journal = The Journal of Biological Chemistry | volume = 279 | issue = 38 | pages = 40146–52 | date = Sep 2004 | pmid = 15199049 | doi = 10.1074/jbc.M405795200 }}
* {{cite journal | vauthors = ((Youm Yun-Hee)), Horvath TL, Mangelsdorf DJ, Kliewer SA, Dixit VD  | title = Prolongevity hormone FGF21 protects against immune senescence by delaying age-related thymic involution | journal = Proceedings of the National Academy of Sciences of the United States of America | pages = 201514511 |year=2016  | doi =10.1073/pnas.1514511113 | volume=113 | pmid=26755598 | pmc=4743827}}
{{refend}}
 
== External links ==
* {{MeshName|fibroblast+growth+factor+21}}
* {{cite web | url = http://www.ihop-net.org/UniPub/iHOP/gismo/97523.html | title = FGF21 | author = | authorlink = | vauthors = | date = | work = [[Information Hyperlinked over Proteins]] | publisher =  ihop-net.org | pages = | archiveurl = | archivedate = | quote = | accessdate = 2008-08-12}}
* {{cite web | url = http://www.genecards.org/cgi-bin/carddisp.pl?gene=FGF21 | title = FGF21 | author = | authorlink = | vauthors = | date = | format = | work = Gene Cards | publisher = Weizmann Institute of Science | pages = | archiveurl = | archivedate = | quote = | accessdate = 2008-08-12}}
*[https://phys.org/news/2017-05-sweet-tooth-blame-liver.html Got a sweet tooth? Blame your liver] [[Phys.org]], 2017
 
{{NLM content}}
{{Growth factors}}
{{Growth factor receptor modulators}}
 
[[Category:Aging-related proteins]]
[[Category:Anti-aging substances]]

Revision as of 09:39, 10 November 2017

VALUE_ERROR (nil)
Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez

n/a

n/a

Ensembl

n/a

n/a

UniProt

n/a

n/a

RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Fibroblast growth factor 21 is a protein that in mammals is encoded by the FGF21 gene.[1][1][2] The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family and specifically a member of the endocrine subfamily which includes FGF23 and FGF15/19.

FGF family members possess broad mitogenic and cell survival activities and are involved in a variety of biological processes including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion.[2] FGFs act through a family of four FGF receptors. Binding is complicated and requires both interaction of the FGF molecule with an FGF receptor and binding to heparin through an heparin binding domain. Endocrine FGFs lack a heparin binding domain and thus can be released into the circulation. FGF21 action through one of the FGF21 receptors thus requires interaction with a co-receptor, designated β-klotho.

Regulation

FGF21 is specifically induced by HMGCS2 activity. The oxidized form of ketone bodies (acetoacetate) in a cultured medium also induced FGF21, possibly via a SIRT1-dependent mechanism.[3] HMGCS2 activity has also been shown to be increased by deacetylation of lysines 310, 447, and 473 via SIRT3 in the mitochondria.[4]

While FGF21 is expressed in numerous tissues, including liver, brown adipose tissue, white adipose tissue and pancreas, circulating levels of FGF21 are derived specifically from the liver in mice.[5] In liver FGF21 expression is regulated by PPARα and levels rise substantially with both fasting and consumption of ketogenic diets.

LXR represses FGF21 in humans via an LXR response element located from -37 to -22 bp on the human FGF21 promoter.[6]

Function

FGF21 stimulates glucose uptake in adipocytes but not in other cell types.[7] This effect is additive to the activity of insulin. FGF21 treatment of adipocytes is associated with phosphorylation of FRS2, a protein linking FGF receptors to the Ras/MAP kinase pathway. FGF21 injection in ob/ob mice results in an increase in Glut1 in adipose tissue. FGF21 also protects animals from diet-induced obesity when overexpressed in transgenic mice and lowers blood glucose and triglyceride levels when administered to diabetic rodents.[7] Treatment of animals with FGF21 results in increased energy expenditure, fat utilization and lipid excretion.[8]

Beta Klotho (KLB) functions as a cofactor essential for FGF21 activity.[9]

In cows plasma FGF21 was nearly undetectable in late pregnancy (LP), peaked at parturition, and then stabilized at lower, chronically elevated concentrations during early lactation (EL). Plasma FGF21 was similarly increased in the absence of parturition when an energy-deficit state was induced by feed restricting late-lactating dairy cows, implicating energy insufficiency as a cause of chronically elevated FGF21 in EL. The liver was the major source of plasma FGF21 in early lactation with little or no contribution by WAT, skeletal muscle, and mammary gland. Meaningful expression of the FGF21 coreceptor β-Klotho was restricted to liver and WAT in a survey of 15 tissues that included the mammary gland. Expression of β-Klotho and its subset of interacting FGF receptors was modestly affected by the transition from LP to EL in liver but not in WAT.[10]

Clinical significance

Serum FGF-21 levels were significantly increased in patients with type 2 diabetes mellitus (T2DM) which may indicate a role in the pathogenesis of T2DM.[11] Elevated levels also correlate with liver fat content in non-alcoholic fatty liver disease[12] and positively correlate with BMI in humans suggesting obesity as a FGF21-resistant state.[13]

Animal studies

Mice lacking FGF21 fail to fully induce PGC-1α expression in response to a prolonged fast and have impaired gluconeogenesis and ketogenesis.[14]

FGF21 stimulates phosphorylation of fibroblast growth factor receptor substrate 2 and ERK1/2 in the liver. Acute FGF21 treatment induced hepatic expression of key regulators of gluconeogenesis, lipid metabolism, and ketogenesis including glucose-6-phosphatase, phosphoenol pyruvate carboxykinase, 3-hydroxybutyrate dehydrogenase type 1, and carnitine palmitoyltransferase 1α. In addition, injection of FGF21 was associated with decreased circulating insulin and free fatty acid levels. FGF21 treatment induced mRNA and protein expression of PGC-1α, but in mice PGC-1α expression was not necessary for the effect of FGF21 on glucose metabolism.[15]

In mice FGF21 is strongly induced in liver by prolonged fasting via PPAR-alpha and in turn induces the transcriptional coactivator PGC-1α and stimulates hepatic gluconeogenesis, fatty acid oxidation, and ketogenesis. FGF21 also blocks somatic growth and sensitizes mice to a hibernation-like state of torpor, playing a key role in eliciting and coordinating the adaptive starvation response. FGF21 expression is also induced in white adipose tissue by PPAR-gamma, which may indicate it also regulates metabolism in the fed state.[16]

Activation of AMPK and SIRT1 by FGF21 in adipocytes enhanced mitochondrial oxidative capacity as demonstrated by increases in oxygen consumption, citrate synthase activity, and induction of key metabolic genes. The effects of FGF21 on mitochondrial function require serine/threonine kinase 11 (STK11/LKB1), which activates AMPK. Inhibition of AMPK, SIRT1, and PGC-1α activities attenuated the effects of FGF21 on oxygen consumption and gene expression, indicating that FGF21 regulates mitochondrial activity and enhances oxidative capacity through an LKB1-AMPK-SIRT1-PGC-1α-dependent mechanism in adipocytes, resulting in increased phosphorylation of AMPK, increased cellular NAD+ levels and activation of SIRT1 and deacetylation of SIRT1 targets PGC-1α and histone 3.[17]

Acutely, the rise in FGF21 in response to alcohol consumption inhibits further drinking. Chronically, the rise in FGF21 expression in the liver may protect against liver damage.

References

  1. ↑ 1.0 1.1 Nishimura T, Nakatake Y, Konishi M, Itoh N (Jun 2000). "Identification of a novel FGF, FGF-21, preferentially expressed in the liver". Biochimica et Biophysica Acta. 1492 (1): 203–6. doi:10.1016/S0167-4781(00)00067-1. PMID 10858549.
  2. ↑ 2.0 2.1 "Entrez Gene: FGF21 fibroblast growth factor 21".
  3. ↑ Vilà-Brau A, De Sousa-Coelho AL, Mayordomo C, Haro D, Marrero PF (Jun 2011). "Human HMGCS2 regulates mitochondrial fatty acid oxidation and FGF21 expression in HepG2 cell line". The Journal of Biological Chemistry. 286 (23): 20423–30. doi:10.1074/jbc.M111.235044. PMC 3121469. PMID 21502324.
  4. ↑ Shimazu T, Hirschey MD, Hua L, Dittenhafer-Reed KE, Schwer B, Lombard DB, Li Y, Bunkenborg J, Alt FW, Denu JM, Jacobson MP, Verdin E (Dec 2010). "SIRT3 deacetylates mitochondrial 3-hydroxy-3-methylglutaryl CoA synthase 2 and regulates ketone body production". Cell Metabolism. 12 (6): 654–61. doi:10.1016/j.cmet.2010.11.003. PMC 3310379. PMID 21109197.
  5. ↑ Markan KR, Naber MC, Ameka MK, Anderegg MD, Mangelsdorf DJ, Kliewer SA, Mohammadi M, Potthoff MJ (Dec 2014). "Circulating FGF21 is liver derived and enhances glucose uptake during refeeding and overfeeding". Diabetes. 63 (12): 4057–63. doi:10.2337/db14-0595. PMC 4238010. PMID 25008183.
  6. ↑ Uebanso T, Taketani Y, Yamamoto H, Amo K, Tanaka S, Arai H, Takei Y, Masuda M, Yamanaka-Okumura H, Takeda E (Jul 2012). "Liver X receptor negatively regulates fibroblast growth factor 21 in the fatty liver induced by cholesterol-enriched diet". The Journal of Nutritional Biochemistry. 23 (7): 785–90. doi:10.1016/j.jnutbio.2011.03.023. PMID 21889884.
  7. ↑ 7.0 7.1 Kharitonenkov A, Shiyanova TL, Koester A, Ford AM, Micanovic R, Galbreath EJ, Sandusky GE, Hammond LJ, Moyers JS, Owens RA, Gromada J, Brozinick JT, Hawkins ED, Wroblewski VJ, Li DS, Mehrbod F, Jaskunas SR, Shanafelt AB (Jun 2005). "FGF-21 as a novel metabolic regulator". The Journal of Clinical Investigation. 115 (6): 1627–35. doi:10.1172/JCI23606. PMC 1088017. PMID 15902306.
  8. ↑ Coskun T, Bina HA, Schneider MA, Dunbar JD, Hu CC, Chen Y, Moller DE, Kharitonenkov A (Dec 2008). "Fibroblast growth factor 21 corrects obesity in mice". Endocrinology. 149 (12): 6018–27. doi:10.1210/en.2008-0816. PMID 18687777.
  9. ↑ Ogawa Y, Kurosu H, Yamamoto M, Nandi A, Rosenblatt KP, Goetz R, Eliseenkova AV, Mohammadi M, Kuro-o M (May 2007). "BetaKlotho is required for metabolic activity of fibroblast growth factor 21". Proceedings of the National Academy of Sciences of the United States of America. 104 (18): 7432–7. Bibcode:2007PNAS..104.7432O. doi:10.1073/pnas.0701600104. PMC 1855074. PMID 17452648.
  10. ↑ Schoenberg KM, Giesy SL, Harvatine KJ, Waldron MR, Cheng C, Kharitonenkov A, Boisclair YR (Dec 2011). "Plasma FGF21 is elevated by the intense lipid mobilization of lactation". Endocrinology. 152 (12): 4652–61. doi:10.1210/en.2011-1425. PMID 21990311.
  11. ↑ Cheng X, Zhu B, Jiang F, Fan H (2011). "Serum FGF-21 levels in type 2 diabetic patients". Endocrine Research. 36 (4): 142–8. doi:10.3109/07435800.2011.558550. PMID 21973233.
  12. ↑ Yan H, Xia M, Chang X, Xu Q, Bian H, Zeng M, Rao S, Yao X, Tu Y, Jia W, Gao X (2011). "Circulating fibroblast growth factor 21 levels are closely associated with hepatic fat content: a cross-sectional study". PLOS ONE. 6 (9): e24895. Bibcode:2011PLoSO...624895Y. doi:10.1371/journal.pone.0024895. PMC 3174975. PMID 21949781.
  13. ↑ Kralisch S, Fasshauer M (Jul 2011). "Fibroblast growth factor 21: effects on carbohydrate and lipid metabolism in health and disease". Current Opinion in Clinical Nutrition and Metabolic Care. 14 (4): 354–9. doi:10.1097/MCO.0b013e328346a326. PMID 21505329.
  14. ↑ Potthoff MJ, Inagaki T, Satapati S, Ding X, He T, Goetz R, Mohammadi M, Finck BN, Mangelsdorf DJ, Kliewer SA, Burgess SC (Jun 2009). "FGF21 induces PGC-1alpha and regulates carbohydrate and fatty acid metabolism during the adaptive starvation response". Proceedings of the National Academy of Sciences of the United States of America. 106 (26): 10853–8. Bibcode:2009PNAS..10610853P. doi:10.1073/pnas.0904187106. PMC 2705613. PMID 19541642.
  15. ↑ Fisher FM, Estall JL, Adams AC, Antonellis PJ, Bina HA, Flier JS, Kharitonenkov A, Spiegelman BM, Maratos-Flier E (Aug 2011). "Integrated regulation of hepatic metabolism by fibroblast growth factor 21 (FGF21) in vivo". Endocrinology. 152 (8): 2996–3004. doi:10.1210/en.2011-0281. PMC 3138239. PMID 21712364.
  16. ↑ Kliewer SA, Mangelsdorf DJ (Jan 2010). "Fibroblast growth factor 21: from pharmacology to physiology". The American Journal of Clinical Nutrition. 91 (1): 254S–257S. doi:10.3945/ajcn.2009.28449B. PMC 2793111. PMID 19906798.
  17. ↑ Chau MD, Gao J, Yang Q, Wu Z, Gromada J (Jul 2010). "Fibroblast growth factor 21 regulates energy metabolism by activating the AMPK-SIRT1-PGC-1alpha pathway". Proceedings of the National Academy of Sciences of the United States of America. 107 (28): 12553–8. Bibcode:2010PNAS..10712553C. doi:10.1073/pnas.1006962107. PMC 2906565. PMID 20616029.

Further reading

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

Retrieved from "https://www.wikidoc.org/index.php?title=FGF21&oldid=1419117"