• Je něco špatně v tomto záznamu ?

Visfatin is actively secreted in vitro from U-937 macrophages, but only passively released from 3T3-L1 adipocytes and HepG2 hepatocytes

P. Svoboda, E. KříŽová, K. Čeňková, K. Vápenková, J. Zídková, V. Zídek, V. Škop

. 2017 ; 66 (4) : 709-714. [pub] 20170412

Jazyk angličtina Země Česko

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc18021066

Visfatin is a multi-functional molecule that can act intracellularly and extracellularly as an adipokine, cytokine and enzyme. One of the main questions concerning visfatin is the mechanism of its secretion; whether, how and from which cells visfatin is released. The objective of this in vitro study was to observe the active secretion of visfatin from 3T3-L1 preadipocytes and adipocytes, HepG2 hepatocytes, U-937, THP-1 and HL-60 monocytes and macrophages. The amount of visfatin in media and cell lysate was always related to the intracellular enzyme, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), to exclude the passive release of visfatin. Visfatin was not found in media of 3T3-L1 preadipocytes. In media of 3T3-L1 adipocytes and HepG2 hepatocytes, the ratio of visfatin to the amount of GAPDH was identical to cell lysates. Hence, it is likely that these cells do not actively secrete visfatin in a significant manner. However, we found that significant producers of visfatin are differentiated macrophages and that the amount of secreted visfatin depends on used cell line and it is affected by the mode of differentiation. Results show that 3T3-L1 adipocytes and HepG2 hepatocytes released visfatin only passively during the cell death. U-937 macrophages secrete visfatin in the greatest level from all of the tested cell lines.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc18021066
003      
CZ-PrNML
005      
20180621135909.0
007      
ta
008      
180611s2017 xr d f 000 0|eng||
009      
AR
024    7_
$a 10.33549/physiolres.933370 $2 doi
035    __
$a (PubMed)28406695
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xr
100    1_
$a Svoboda, Petr $u Department of Biochemistry and Microbiology, University of Chemistry and Technology, Prague, Czech Republic; Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic $7 xx0140547
245    10
$a Visfatin is actively secreted in vitro from U-937 macrophages, but only passively released from 3T3-L1 adipocytes and HepG2 hepatocytes / $c P. Svoboda, E. KříŽová, K. Čeňková, K. Vápenková, J. Zídková, V. Zídek, V. Škop
520    9_
$a Visfatin is a multi-functional molecule that can act intracellularly and extracellularly as an adipokine, cytokine and enzyme. One of the main questions concerning visfatin is the mechanism of its secretion; whether, how and from which cells visfatin is released. The objective of this in vitro study was to observe the active secretion of visfatin from 3T3-L1 preadipocytes and adipocytes, HepG2 hepatocytes, U-937, THP-1 and HL-60 monocytes and macrophages. The amount of visfatin in media and cell lysate was always related to the intracellular enzyme, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), to exclude the passive release of visfatin. Visfatin was not found in media of 3T3-L1 preadipocytes. In media of 3T3-L1 adipocytes and HepG2 hepatocytes, the ratio of visfatin to the amount of GAPDH was identical to cell lysates. Hence, it is likely that these cells do not actively secrete visfatin in a significant manner. However, we found that significant producers of visfatin are differentiated macrophages and that the amount of secreted visfatin depends on used cell line and it is affected by the mode of differentiation. Results show that 3T3-L1 adipocytes and HepG2 hepatocytes released visfatin only passively during the cell death. U-937 macrophages secrete visfatin in the greatest level from all of the tested cell lines.
650    _2
$a buňky 3T3-L1 $7 D041721
650    _2
$a tukové buňky $x sekrece $7 D017667
650    _2
$a zvířata $7 D000818
650    _2
$a buňky Hep G2 $7 D056945
650    _2
$a hepatocyty $x sekrece $7 D022781
650    _2
$a lidé $7 D006801
650    _2
$a makrofágy $x sekrece $7 D008264
650    _2
$a myši $7 D051379
650    _2
$a nikotinamidfosforibosyltransferasa $x sekrece $7 D054409
650    _2
$a U937 buňky $7 D020298
655    _2
$a časopisecké články $7 D016428
700    1_
$a Křížová, Edita $7 _AN075182 $u Department of Biochemistry and Microbiology, University of Chemistry and Technology, Prague, Czech Republic
700    1_
$a Čeňková, Kateřina. $7 xx0258043 $u Department of Biochemistry and Microbiology, University of Chemistry and Technology, Prague, Czech Republic
700    1_
$a Vápenková, K. $7 _AN096618 $u Department of Biochemistry and Microbiology, University of Chemistry and Technology, Prague, Czech Republic
700    1_
$a Zídková, Jarmila $7 xx0074470 $u Department of Biochemistry and Microbiology, University of Chemistry and Technology, Prague, Czech Republic
700    1_
$a Zídek, Václav, $d 1951- $7 xx0088482 $u Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic
700    1_
$a Škop, Vojtěch $7 xx0121451 $u Department of Biochemistry and Microbiology, University of Chemistry and Technology, Prague, Czech Republic
773    0_
$w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 66, č. 4 (2017), s. 709-714
856    41
$u https://pubmed.ncbi.nlm.nih.gov/28406695 $y Pubmed
910    __
$a ABA008 $b A 4120 $c 266 $y 4 $z 0
990    __
$a 20180611 $b ABA008
991    __
$a 20180619133959 $b ABA008
999    __
$a ok $b bmc $g 1311780 $s 1017938
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2017 $b 66 $c 4 $d 709-714 $e 20170412 $i 1802-9973 $m Physiological research $n Physiol. Res. (Print) $x MED00003824
LZP    __
$b NLK118 $a Pubmed-20180611

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...