-
Je něco špatně v tomto záznamu ?
Mitochondrial respiration of adipocytes differentiating from human mesenchymal stem cells derived from adipose tissue
I. Kladnická, M. Čedíková, M. Kripnerová, J. Dvořáková, M. Kohoutová, Z. Tůma, D. Müllerová, J. Kuncová
Jazyk angličtina Země Česko
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 1991
Free Medical Journals
od 1998
ProQuest Central
od 2005-01-01
Medline Complete (EBSCOhost)
od 2006-01-01
Nursing & Allied Health Database (ProQuest)
od 2005-01-01
Health & Medicine (ProQuest)
od 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
od 1998
- MeSH
- adipogeneze * MeSH
- buněčné dýchání MeSH
- kultivované buňky MeSH
- lidé MeSH
- membránový potenciál mitochondrií MeSH
- metabolismus lipidů MeSH
- mezenchymální kmenové buňky fyziologie MeSH
- mitochondrie metabolismus MeSH
- tukové buňky metabolismus MeSH
- Check Tag
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
Burden of obesity is increasing in the contemporary world. Although multifactorial in origin, appropriate mitochondrial function of adipocytes emerges as a factor essential for healthy adipocyte differentiation and adipose tissue function. Our study aimed to evaluate mitochondrial functions of human adipose-derived mesenchymal stem cells committed to adipogenesis. On days 0, 4, 10, and 21 of adipogenesis, we have characterized adipocyte proliferation and viability, quantified lipid accumulation in maturing cells, performed qualitative and quantitative analysis of mitochondria, determined mitochondrial respiration of cells using high-resolution respirometry, and evaluated mitochondrial membrane potential. In the course of adipogenesis, mitochondrial oxygen consumption progressively increased in states ROUTINE and E (capacity of the electron transfer system). State LEAK remained constant during first days of adipogenesis and then increased probably reflecting uncoupling ability of maturing adipocytes. Citrate synthase activity and volume of mitochondrial networks increased during differentiation, particularly between days 10 and 21. In addition, lipid accumulation remained low until day 10 and then significantly increased. In conclusion, during first days of adipogenesis, increased mitochondrial respiration is needed for transition of differentiating cells from glycolytic to oxidative metabolism and clonal expansion of preadipocytes and then more energy is needed to acquire typical metabolic phenotype of mature adipocyte.
Biomedical Center Faculty of Medicine in Pilsen Charles University Pilsen Czech Republic
Institute of Biology Faculty of Medicine in Pilsen Charles University Pilsen Czech Republic
Institute of Physiology Faculty of Medicine in Pilsen Charles University Pilsen Czech Republic
Citace poskytuje Crossref.org
Literatura
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21028187
- 003
- CZ-PrNML
- 005
- 20220328172125.0
- 007
- ta
- 008
- 211105s2019 xr ad f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.934353 $2 doi
- 035 __
- $a (PubMed)31928046
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Kladnická, Iva $7 xx0229226 $u Department of Public Health and Preventive Medicine, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic $u NTIS, European Center of Excellence New Technologies for the Information Society, University of West Bohemia, Pilsen, Czech Republic
- 245 10
- $a Mitochondrial respiration of adipocytes differentiating from human mesenchymal stem cells derived from adipose tissue / $c I. Kladnická, M. Čedíková, M. Kripnerová, J. Dvořáková, M. Kohoutová, Z. Tůma, D. Müllerová, J. Kuncová
- 504 __
- $a Literatura
- 520 9_
- $a Burden of obesity is increasing in the contemporary world. Although multifactorial in origin, appropriate mitochondrial function of adipocytes emerges as a factor essential for healthy adipocyte differentiation and adipose tissue function. Our study aimed to evaluate mitochondrial functions of human adipose-derived mesenchymal stem cells committed to adipogenesis. On days 0, 4, 10, and 21 of adipogenesis, we have characterized adipocyte proliferation and viability, quantified lipid accumulation in maturing cells, performed qualitative and quantitative analysis of mitochondria, determined mitochondrial respiration of cells using high-resolution respirometry, and evaluated mitochondrial membrane potential. In the course of adipogenesis, mitochondrial oxygen consumption progressively increased in states ROUTINE and E (capacity of the electron transfer system). State LEAK remained constant during first days of adipogenesis and then increased probably reflecting uncoupling ability of maturing adipocytes. Citrate synthase activity and volume of mitochondrial networks increased during differentiation, particularly between days 10 and 21. In addition, lipid accumulation remained low until day 10 and then significantly increased. In conclusion, during first days of adipogenesis, increased mitochondrial respiration is needed for transition of differentiating cells from glycolytic to oxidative metabolism and clonal expansion of preadipocytes and then more energy is needed to acquire typical metabolic phenotype of mature adipocyte.
- 650 _2
- $a tukové buňky $x metabolismus $7 D017667
- 650 12
- $a adipogeneze $7 D050156
- 650 _2
- $a buněčné dýchání $7 D019069
- 650 _2
- $a kultivované buňky $7 D002478
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a metabolismus lipidů $7 D050356
- 650 _2
- $a membránový potenciál mitochondrií $7 D053078
- 650 _2
- $a mezenchymální kmenové buňky $x fyziologie $7 D059630
- 650 _2
- $a mitochondrie $x metabolismus $7 D008928
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Čedíková, Miroslava $7 xx0099423 $u Institute of Physiology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic $u Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic
- 700 1_
- $a Kripnerová, Michaela $7 xx0232916 $u Institute of Biology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic
- 700 1_
- $a Dvořáková, Jana $7 _AN070612 $u Institute of Medical Chemistry and Biochemistry, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic
- 700 1_
- $a Kohoutová, Michaela $7 xx0230637 $u Institute of Physiology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic $u Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic
- 700 1_
- $a Tůma, Zdeněk, $d 1980- $7 xx0128863 $u Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic
- 700 1_
- $a Müllerová, Dana, $d 1962- $7 xx0011940 $u Department of Public Health and Preventive Medicine, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic $u NTIS, European Center of Excellence New Technologies for the Information Society, University of West Bohemia, Pilsen, Czech Republic
- 700 1_
- $a Kuncová, Jitka, $d 1964- $7 xx0078884 $u Institute of Physiology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic $u Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic
- 773 0_
- $w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 68, Suppl 3 (2019), s. S287-S296
- 773 0_
- $t Proceedings of the ... Physiological days $g (2019), s. S287-S296 $w MED00183838
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31928046 $y Pubmed
- 910 __
- $a ABA008 $b A 4120 $c 266 $y p $z 0
- 990 __
- $a 20211105 $b ABA008
- 991 __
- $a 20220328172123 $b ABA008
- 999 __
- $a ok $b bmc $g 1735508 $s 1148732
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 68 $c Suppl 3 $d S287-S296 $e 20191220 $i 1802-9973 $m Physiological research $n Physiol. Res. (Print) $x MED00003824
- BMC __
- $a 2019 $d S287-S296 $m Proceedings of the ... Physiological days $x MED00183838
- LZP __
- $b NLK118 $a Pubmed-20211105