-
Je něco špatně v tomto záznamu ?
Adipogenesis, lipogenesis and lipolysis is stimulated by mild but not severe hypoxia in 3T3-L1 cells
M. Weiszenstein, M. Musutova, A. Plihalova, K. Westlake, M. Elkalaf, M. Koc, A. Prochazka, J. Pala, S. Gulati, J. Trnka, J. Polak,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
Grantová podpora
NV15-30155A
MZ0
CEP - Centrální evidence projektů
- MeSH
- acetylkoenzym A metabolismus MeSH
- adipogeneze účinky léků genetika MeSH
- ATP-citrát-(pro-S)-lyasa genetika metabolismus MeSH
- buněčná diferenciace účinky léků MeSH
- buňky 3T3-L1 MeSH
- citrátový cyklus účinky léků genetika MeSH
- diacylglycerol-O-acyltransferasa genetika metabolismus MeSH
- faktor 1 indukovatelný hypoxií - podjednotka alfa genetika metabolismus MeSH
- hypoxie buňky MeSH
- kyslík farmakologie MeSH
- lipidová tělíska chemie účinky léků MeSH
- lipogeneze účinky léků genetika MeSH
- lipolýza účinky léků genetika MeSH
- myši MeSH
- perilipin 1 genetika metabolismus MeSH
- proteiny vázající mastné kyseliny genetika metabolismus MeSH
- regulace genové exprese účinky léků MeSH
- signální transdukce MeSH
- sterolesterasa genetika metabolismus MeSH
- triglyceridy metabolismus MeSH
- tukové buňky cytologie účinky léků metabolismus MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
In-vitro investigation of the effects of hypoxia is limited by physical laws of gas diffusion and cellular O2 consumption, making prolonged exposures to stable O2 concentrations impossible. Using a gas-permeable cultureware, chronic effects of mild and severe hypoxia on triglyceride accumulation, lipid droplet size distribution, spontaneous lipolysis and gene expression of adipocyte-specific markers were assessed. 3T3-L1 cells were differentiated under 20%, 4% or 1% O2 using a gas-permeable cultureware. Triglyceride accumulation, expression of genes characteristic for advanced adipocyte differentiation and involvement of key lipogenesis enzymes were assessed after exposures. Lipogenesis increased by 375% under mild hypoxia, but dropped by 43% in severe hypoxia. Mild, but not severe, hypoxia increased formation of large lipid droplets 6.4 fold and strongly induced gene expression of adipocyte-specific markers. Spontaneous lipolysis increased by 488% in mild, but only by 135% in severe hypoxia. Inhibition of ATP-dependent citrate lyase suppressed hypoxia-induced lipogenesis by 81% and 85%. Activation of HIF inhibited lipogenesis by 59%. Mild, but not severe, hypoxia stimulates lipolysis and promotes adipocyte differentiation, probably through excess of acetyl-CoA originating from tricarboxylic acid cycle independently of HIF activation.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc17023798
- 003
- CZ-PrNML
- 005
- 20201102101434.0
- 007
- ta
- 008
- 170720s2016 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.bbrc.2016.08.015 $2 doi
- 035 __
- $a (PubMed)27498031
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Weiszenstein, Martin $u Center for Research on Diabetes, Metabolism and Nutrition, Third Faculty of Medicine, Charles University in Prague, Ruska 87, Prague, Czech Republic.
- 245 10
- $a Adipogenesis, lipogenesis and lipolysis is stimulated by mild but not severe hypoxia in 3T3-L1 cells / $c M. Weiszenstein, M. Musutova, A. Plihalova, K. Westlake, M. Elkalaf, M. Koc, A. Prochazka, J. Pala, S. Gulati, J. Trnka, J. Polak,
- 520 9_
- $a In-vitro investigation of the effects of hypoxia is limited by physical laws of gas diffusion and cellular O2 consumption, making prolonged exposures to stable O2 concentrations impossible. Using a gas-permeable cultureware, chronic effects of mild and severe hypoxia on triglyceride accumulation, lipid droplet size distribution, spontaneous lipolysis and gene expression of adipocyte-specific markers were assessed. 3T3-L1 cells were differentiated under 20%, 4% or 1% O2 using a gas-permeable cultureware. Triglyceride accumulation, expression of genes characteristic for advanced adipocyte differentiation and involvement of key lipogenesis enzymes were assessed after exposures. Lipogenesis increased by 375% under mild hypoxia, but dropped by 43% in severe hypoxia. Mild, but not severe, hypoxia increased formation of large lipid droplets 6.4 fold and strongly induced gene expression of adipocyte-specific markers. Spontaneous lipolysis increased by 488% in mild, but only by 135% in severe hypoxia. Inhibition of ATP-dependent citrate lyase suppressed hypoxia-induced lipogenesis by 81% and 85%. Activation of HIF inhibited lipogenesis by 59%. Mild, but not severe, hypoxia stimulates lipolysis and promotes adipocyte differentiation, probably through excess of acetyl-CoA originating from tricarboxylic acid cycle independently of HIF activation.
- 650 _2
- $a buňky 3T3-L1 $7 D041721
- 650 _2
- $a ATP-citrát-(pro-S)-lyasa $x genetika $x metabolismus $7 D001275
- 650 _2
- $a acetylkoenzym A $x metabolismus $7 D000105
- 650 _2
- $a tukové buňky $x cytologie $x účinky léků $x metabolismus $7 D017667
- 650 _2
- $a adipogeneze $x účinky léků $x genetika $7 D050156
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a buněčná diferenciace $x účinky léků $7 D002454
- 650 _2
- $a hypoxie buňky $7 D015687
- 650 _2
- $a citrátový cyklus $x účinky léků $x genetika $7 D002952
- 650 _2
- $a diacylglycerol-O-acyltransferasa $x genetika $x metabolismus $7 D051048
- 650 _2
- $a vztah mezi dávkou a účinkem léčiva $7 D004305
- 650 _2
- $a proteiny vázající mastné kyseliny $x genetika $x metabolismus $7 D050556
- 650 _2
- $a regulace genové exprese $x účinky léků $7 D005786
- 650 _2
- $a faktor 1 indukovatelný hypoxií - podjednotka alfa $x genetika $x metabolismus $7 D051795
- 650 _2
- $a lipidová tělíska $x chemie $x účinky léků $7 D066292
- 650 _2
- $a lipogeneze $x účinky léků $x genetika $7 D050155
- 650 _2
- $a lipolýza $x účinky léků $x genetika $7 D008066
- 650 _2
- $a myši $7 D051379
- 650 _2
- $a kyslík $x farmakologie $7 D010100
- 650 _2
- $a perilipin 1 $x genetika $x metabolismus $7 D000070778
- 650 _2
- $a signální transdukce $7 D015398
- 650 _2
- $a sterolesterasa $x genetika $x metabolismus $7 D002787
- 650 _2
- $a triglyceridy $x metabolismus $7 D014280
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Musutova, Martina $u Center for Research on Diabetes, Metabolism and Nutrition, Third Faculty of Medicine, Charles University in Prague, Ruska 87, Prague, Czech Republic.
- 700 1_
- $a Plihalova, Andrea $u Center for Research on Diabetes, Metabolism and Nutrition, Third Faculty of Medicine, Charles University in Prague, Ruska 87, Prague, Czech Republic.
- 700 1_
- $a Westlake, Katerina $u Center for Research on Diabetes, Metabolism and Nutrition, Third Faculty of Medicine, Charles University in Prague, Ruska 87, Prague, Czech Republic; Center of Toxicology and Health Safety, The National Institute of Public Health, Srobarova 48, Prague, Czech Republic.
- 700 1_
- $a Elkalaf, Moustafa $u Laboratory for Metabolism and Bioenergetics, Third Faculty of Medicine, Charles University in Prague, Ruska 87, Prague, Czech Republic.
- 700 1_
- $a Koc, Michal $u Department of Sport Medicine, Third Faculty of Medicine, Charles University in Prague, Ruska 87, Prague, Czech Republic.
- 700 1_
- $a Prochazka, Antonin $u Institute of Biophysics and Informatics, First Faculty of Medicine, Charles University in Prague, Salmovska 1, Prague, Czech Republic.
- 700 1_
- $a Pala, Jan $u Department of Sport Medicine, Third Faculty of Medicine, Charles University in Prague, Ruska 87, Prague, Czech Republic.
- 700 1_
- $a Gulati, Sumeet $u Center for Research on Diabetes, Metabolism and Nutrition, Third Faculty of Medicine, Charles University in Prague, Ruska 87, Prague, Czech Republic.
- 700 1_
- $a Trnka, Jan $u Laboratory for Metabolism and Bioenergetics, Third Faculty of Medicine, Charles University in Prague, Ruska 87, Prague, Czech Republic.
- 700 1_
- $a Polak, Jan $u Center for Research on Diabetes, Metabolism and Nutrition, Third Faculty of Medicine, Charles University in Prague, Ruska 87, Prague, Czech Republic; Center of Toxicology and Health Safety, The National Institute of Public Health, Srobarova 48, Prague, Czech Republic. Electronic address: jan.polak@lf3.cuni.cz.
- 773 0_
- $w MED00009307 $t Biochemical and biophysical research communications $x 1090-2104 $g Roč. 478, č. 2 (2016), s. 727-32
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/27498031 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20170720 $b ABA008
- 991 __
- $a 20201102101434 $b ABA008
- 999 __
- $a ok $b bmc $g 1239479 $s 984711
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2016 $b 478 $c 2 $d 727-32 $e 20160804 $i 1090-2104 $m Biochemical and biophysical research communications $n Biochem Biophys Res Commun $x MED00009307
- GRA __
- $a NV15-30155A $p MZ0
- LZP __
- $a Pubmed-20170720