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001-es BibID:BIBFORM078217
035-os BibID:(Wos)000437674103108
Első szerző:Klusóczki Ágnes (biotechnológus)
Cím:SGBS preadipocyte cell line can serve for human beige type of thermogenic browning adipocyte differentiation / A. Klusóczki, E. Kristóf, P. Fischer-Posovszky, M. Wabitsch, Z. Bacsó, L. Fésüs
Dátum:2018
ISSN:2211-5463
Tárgyszavak:Orvostudományok Elméleti orvostudományok poszter
folyóiratcikk
Megjelenés:FEBS Open Bio. - 8 : S1 (2018), p. 241-242. -
További szerzők:Kristóf Endre (1987-) (általános orvos) Fischer-Posovszky Pamela Wabitsch, Martin Bacsó Zsolt (1963-) (biofizikus) Fésüs László (1947-) (orvos biokémikus)
Internet cím:Szerző által megadott URL
DOI
Intézményi repozitóriumban (DEA) tárolt változat
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2.

001-es BibID:BIBFORM077898
035-os BibID:(cikkazonosító)5823 (PMID)30967578 (WOS)000463869800025 (Scopus)85064055586
Első szerző:Klusóczki Ágnes (biotechnológus)
Cím:Differentiating SGBS adipocytes respond to PPAR gamma stimulation, irisin and BMP7 by functional browning and beige characteristics / Ágnes Klusóczki, Zoltán Veréb, Attila Vámos, Pamela Fischer-Posovszky, Martin Wabitsch, Zsolt Bacso, László Fésüs, Endre Kristóf
Dátum:2019
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Megjelenés:Scientific Reports. - 9 : 1 (2019), p. 1-35. -
További szerzők:Veréb Zoltán (1980-) (immunológus, mikrobiológus, molekuláris biológus) Vámos Attila (1991-) (gyógyszer-biotechnológus) Fischer-Posovszky Pamela Wabitsch, Martin Bacsó Zsolt (1963-) (biofizikus) Fésüs László (1947-) (orvos biokémikus) Kristóf Endre (1987-) (általános orvos)
Pályázati támogatás:GINOP-2.3.2-15-2016-00006
GINOP
OTKA-NK105046
OTKA
ÚNKP-18-4
ÚNKP
Internet cím:Intézményi repozitóriumban (DEA) tárolt változat
DOI
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3.

001-es BibID:BIBFORM077512
Első szerző:Kristóf Endre (általános orvos)
Cím:Interleukin-6 released from differentiating human beige adipocytes improves browning / Endre Kristóf, Ágnes Klusóczki, Roland Veress, Abhirup Shaw, Zsolt Sándor Combi, Klára Varga, Ferenc Győry, Zoltán Balajthy, Péter Bai, Zsolt Bacso, László Fésüs
Dátum:2019
ISSN:0014-4827
Megjegyzések:Brown and beige adipocytes contribute significantly to the regulation of whole body energy expenditure and systemic metabolic homeostasis not exclusively by thermogenesis through mitochondrial uncoupling. Several studies have provided evidence in rodents that brown and beige adipocytes produce a set of adipokines ("batokines") which regulate local tissue homeostasis and have beneficial effects on physiological functions of the entire body. We observed elevated secretion of Interleukin (IL)-6, IL-8 and monocyte chemoattractant protein (MCP)-1, but not tumor necrosis factor alpha (TNFα) or IL-1β pro-inflammatory cytokines, by ex vivo differentiating human beige adipocytes (induced by either PPARγ agonist or irisin) compared to white. Higher levels of IL-6, IL-8 and MCP-1 were released from human deep neck adipose tissue biopsies (enriched in browning cells) than from subcutaneous ones. IL-6 was produced in a sustained manner and mostly by the adipocytes and not by the undifferentiated progenitors. Continuous blocking of IL-6 receptor by specific antibody during beige differentiation resulted in downregulation of brown marker genes and increased morphological changes that are characteristic of white adipocytes. The data suggest that beige adipocytes adjust their production of IL-6 to reach an optimal level for differentiation in the medium enhancing browning in an autocrine manner.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Experimental Cell Research. - 377 : 1-2 (2019), p. 47-55. -
További szerzők:Klusóczki Ágnes (1991-) (biotechnológus) Veress Roland (1992-) (molekuláris biológus) Shaw, Abhirup (1992-) Combi Zsolt (1981-) Varga Klára Győry Ferenc (1969-) (kardiológus) Balajthy Zoltán (1957-) (biokémikus, sejtbiológus) Bai Péter (1976-) (biokémikus) Bacsó Zsolt (1963-) (biofizikus) Fésüs László (1947-) (orvos biokémikus)
Pályázati támogatás:GINOP-2.3.2-15-2016-00006
GINOP
OTKA-NK105046
OTKA
OTKA-K123975
OTKA
ÚNKP-18-4
ÚNKP
Internet cím:Szerző által megadott URL
DOI
Intézményi repozitóriumban (DEA) tárolt változat
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4.

001-es BibID:BIBFORM067761
Első szerző:Kristóf Endre (általános orvos)
Cím:Browning-inducers modify the differentiation of human adipocytes from different anatomical sites and enhance their mitochondrial respiration / Kristóf Endre, Quang-Minh Doan-Xuan, Klusóczki Ágnes, Győry Ferenc, Póliska Szilárd, Bacsó Zsolt, Bai Péter, Fésüs László
Dátum:2016
Megjegyzések:Several studies highlighted the strong negative correlation between obesity and active brown adipose tissue amount in adult humans. There are at least two types of thermogenic fat depots, classical brown and beige, which have different origins and tissue distribution. We intended to clarify whether preadipocytes from different anatomical sites are capable of initiating a browning program in parallel with the enhancement of mitochondrial respiration in response to browning-inducers. Preadipocytes obtained from herniotomy (abdominal subcutaneous) or thyroid surgery ("deep neck" and cervical subcutaneous) and a human preadipocyte cell line (SGBS) were differentiated into white, brown (by BMP7 treatment) or beige (by irisin and clozapine administration or by a previously described cocktail) adipocytes. To assess browning, gene expression measurements and laser-scanning cytometry based morphology analysis were performed. Oxygen consumption was measured using an XF96 oxymeter. Differentiating adipocytes treated with browning-inducers had smaller lipid droplets, more mitochondrial DNA, higher mitochondrial respiration and contained more Ucp1 protein than white adipocytes. Browning adipocytes utilize more fatty acids by beta-oxidation and increase their respiration by activating a futile cycle of creatine metabolism. Next, we intend to identify molecular markers to characterize those preadipocytes that are capable to implement an effective browning program.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idézhető absztrakt
Megjelenés:Journal of World Mitochondria Society. - 2 : 2 (2016), p. 23. -
További szerzők:Doan-Xuan, Quang-Minh (1986-) (biofizikus) Klusóczki Ágnes (1991-) (biotechnológus) Győry Ferenc (1969-) (kardiológus) Póliska Szilárd (1978-) (biológus) Bacsó Zsolt (1963-) (biofizikus) Bai Péter (1976-) (biokémikus) Fésüs László (1947-) (orvos biokémikus)
Pályázati támogatás:NK 105046
OTKA
GINOP-2.3.2-15-2016-00006
GINOP
Internet cím:Szerző által megadott URL
DOI
Intézményi repozitóriumban (DEA) tárolt változat
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5.

001-es BibID:BIBFORM066378
Első szerző:Kristóf Endre (általános orvos)
Cím:Differentiating human beige adipocytes secrete cytokines ("batokines") / Endre Kristóf, Ágnes Klusóczki, Zsolt Combi, Roland Veress, Ferenc Győry, Szilárd Póliska, Zsolt Bacsó, László Fésüs
Dátum:2016
Megjegyzések:Several studies highlighted the strong negative correlation between obesity and metabolically active brown adipose tissue amount in adult humans. There are at least two types of thermogenic fat depots, classical brown and beige, which have different origins and tissue distribution. Beige adipocytes contribute to the regulation of systemic metabolic homeostasis not exclusively by thermogenesis and mitochondrial uncoupling. In the present study, we investigated the secretion of "batokines" by primary human brown and beige adipocytes and by human adipose tissue samples. Adipose-derived mesenchymal stem cells obtained from herniotomy (abdominal subcutaneous) or thyroid surgery ("deep neck" and cervical subcutaneous) and a human preadipocyte cell line (SGBS) were differentiated into white, brown (by BMP7 treatment) or beige (by irisin administration or by a previously described cocktail) adipocytes. Cytokine gene expression in browning adipocytes was determined by RNA sequencing. Conditioned differentiation media were collected during the replacement of the adipogenic cocktails and secreted IL-6, IL-8, TNF?, MCP-1 and IL1-? were measured by ELISA. IL-6, MCP-1 and IL-8 secretion was significantly higher by beige compared to white adipocytes. In contrast to BMP7 administration (when classical brown adipocyte differentiation occurs), irisin treatment (which induces beige adipocyte differentiation) resulted in an increased total IL-6, MCP-1 and IL-8 production. Media collected daily or after three day periods contained the same amount of IL-6 depending only on the phase of differentiation. This suggests that adipocytes adjusted their production of the cytokine to reach an optimal level in the medium. In the heterogeneous population of differentiating adipocytes, IL-6 containing vesicles could be visualized mostly in beige cells by Laser-scanning cytometry. In the future we intend to explore the functional significance of the produced "batokines".
Tárgyszavak:Orvostudományok Elméleti orvostudományok idézhető absztrakt
Megjelenés:Biokémia. - 40 : 3 (2016), p. 37. -
További szerzők:Klusóczki Ágnes (1991-) (biotechnológus) Combi Zsolt (1981-) Veress Roland (1992-) (molekuláris biológus) Győry Ferenc (1969-) (kardiológus) Póliska Szilárd (1978-) (biológus) Bacsó Zsolt (1963-) (biofizikus) Fésüs László (1947-) (orvos biokémikus)
Pályázati támogatás:TÁMOP-4.2.2.A-11/1/KONV-2012-0023
TÁMOP
TÁMOP-4.2.2.A-11/1/KONV-2012-0025
TÁMOP
TRANSCOM IAPP 251506
FP7
MTA-DE
MTA
Apoptózis és Genomika Kutatócsoport
NK105046
OTKA
GINOP-2.3.2-15-2016-00006
GINOP
Internet cím:Intézményi repozitóriumban (DEA) tárolt változat
Borító:

6.

001-es BibID:BIBFORM065903
035-os BibID:(Scopus)85030708620 (WOS)000392133700005
Első szerző:Kristóf Endre (általános orvos)
Cím:Clozapine modifies the differentiation program of human adipocytes inducing browning / Endre Kristóf, Quang-Minh Doan-Xuan, Anitta Kinga Sárvári, Ágnes Klusóczki, Pamela Fischer-Posovszky, Martin Wabitsch, Zsolt Bacso, Péter Bai, Zoltán Balajthy, László Fésüs
Dátum:2016
Megjegyzések:Administration of second-generation antipsychotic drugs (SGAs) often leads to weight gain and consequent cardio-metabolic side effects. We observed that clozapine but not 6 other antipsychotic drugs reprogrammed the gene expression pattern of differentiating human adipocytes ex vivo, leading to an elevated expression of the browning marker gene UCP1, more and smaller lipid droplets and more mitochondrial DNA than in the untreated white adipocytes. Laser-scanning cytometry showed that up to 40% of the differentiating single primary and SGBS adipocytes had the characteristic morphological features of browning cells. Furthermore, clozapine significantly up-regulated ELOVL3, CIDEA, CYC1, PGC1A and TBX1 genes but not ZIC1 suggesting induction of the beige-like and not the classical brown phenotype. When we tested if browning induced by clozapine can be explained by its known pharmacological effect of antagonizing serotonin (5HT) receptors it was found that browning cells expressed 5HT receptors 2A, 1D, 7 and the up-regulation of browning markers was diminished in the presence of exogenous 5HT. Undifferentiated progenitors or completely differentiated beige or white adipocytes did not respond to clozapine administration. The clozapine induced beige cells displayed increased basal and oligomycin inhibited (proton leak) oxygen consumption but these cells showed a lower response to cAMP stimulus as compared to control beige adipocytes indicating that they are less capable to respond to natural thermogenic anti-obesity cues. Our data altogether suggest that novel pharmacological stimulation of these masked beige adipocytes can be a future therapeutic target for treatment of SGA-induced weight gain.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
adipocita
beige
clozapine
lézer-pásztázó citometria
elhízás
szerotonin
termogenezis
Megjelenés:Translational Psychiatry. - 6 : 11 (2016), p. 1-12. -
További szerzők:Doan-Xuan, Quang-Minh (1986-) (biofizikus) Sárvári Anitta Kinga (1984-) (biológus) Klusóczki Ágnes (1991-) (biotechnológus) Fischer-Posovszky Pamela Wabitsch, Martin Bacsó Zsolt (1963-) (biofizikus) Bai Péter (1976-) (biokémikus) Balajthy Zoltán (1957-) (biokémikus, sejtbiológus) Fésüs László (1947-) (orvos biokémikus)
Pályázati támogatás:TÁMOP-4.2.4.A/2-11/1-2012-0001
TÁMOP
TÁMOP-4.2.2.A-11/1/KONV-2012-0023
TÁMOP
TÁMOP-4.2.2.A-11/1/KONV-2012-0025
TÁMOP
TRANSCOM IAPP 251506
FP7
MTA-DE
MTA
Apoptózis és Genomika Kutatócsoport
K108308
OTKA
NK105046
OTKA
GINOP-2.3.2-15-2016-00006
GINOP
Internet cím:Intézményi repozitóriumban (DEA) tárolt változat
DOI
Borító:
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