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1.
Immun Ageing ; 20(1): 51, 2023 Oct 11.
Artigo em Inglês | MEDLINE | ID: mdl-37821967

RESUMO

BACKGROUND: Adipose-derived stem cells (ADSC) are multipotent cells implicated in tissue homeostasis. Obesity represents a chronic inflammatory disease associated with metabolic dysfunction and age-related mechanisms, with progressive accumulation of senescent cells and compromised ADSC function. In this study, we aimed to explore mechanisms associated with the inflammatory environment present in obesity in modulating ADSC to a senescent phenotype. We evaluated phenotypic and functional alterations through 18 days of treatment. ADSC were cultivated with a conditioned medium supplemented with a pool of plasma from eutrophic individuals (PE, n = 15) or with obesity (PO, n = 14), and compared to the control. RESULTS: Our results showed that PO-treated ADSC exhibited decreased proliferative capacity with G2/M cycle arrest and CDKN1A (p21WAF1/Cip1) up-regulation. We also observed increased senescence-associated ß-galactosidase (SA-ß-gal) activity, which was positively correlated with TRF1 protein expression. After 18 days, ADSC treated with PO showed augmented CDKN2A (p16INK4A) expression, which was accompanied by a cumulative nuclear enlargement. After 10 days, ADSC treated with PO showed an increase in NF-κB phosphorylation, while PE and PO showed an increase in p38MAPK activation. PE and PO treatment also induced an increase in senescence-associated secretory phenotype (SASP) cytokines IL-6 and IL-8. PO-treated cells exhibited decreased metabolic activity, reduced oxygen consumption related to basal respiration, increased mitochondrial depolarization and biomass, and mitochondrial network remodeling, with no superoxide overproduction. Finally, we observed an accumulation of lipid droplets in PO-treated ADSC, implying an adaptive cellular mechanism induced by the obesogenic stimuli. CONCLUSIONS: Taken together, our data suggest that the inflammatory environment observed in obesity induces a senescent phenotype associated with p38MAPK/NF-κB axis, which stimulates and amplifies the SASP and is associated with impaired mitochondrial homeostasis.

2.
Cytokine ; 56(3): 600-7, 2011 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-21930390

RESUMO

Gangliosides have been extensively described to be involved in the proliferation and differentiation of various cell types, such including hematopoietic cells. Our previous studies on murine models of stroma-mediated myelopoiesis have shown that gangliosides are required for optimal capacity of stromal cells to support proliferation of myeloid precursor cells, being shed to the supernatant and selectively incorporated into myeloid cell membranes. Here we describe the effect of gangliosides on the specific granulocyte-macrophage colony-stimulating factor (GM-CSF)-induced proliferation. For that, we used the monocytic FDC-P1 cell line, which is dependent upon GM-CSF for survival and proliferation. Cells were cultured in the presence of GM-CSF and exogenous gangliosides (GM3, GD1a or GM1) or in the absence of endogenous ganglioside synthesis by the use of a ceramide-synthase inhibitor, D-PDMP. We observed that exogenous addition of GD1a enhanced the GM-CSF-induced proliferation of the FDC-P1 cells. Also, we detected an increase in the expression of the α isoform of the GM-CSF receptor (GMRα) as well as of the transcription factor C/EBPα. On the contrary, inhibition of glucosylceramide synthesis was accompanied by a decrease in cell proliferation, which was restored upon the addition of exogenous GD1a. We also show a co-localization of GD1a and GMR by immunocytochemistry. Taken together, our results suggest for the first time that ganglioside GD1a play a role on the modulation of GM-CSF-mediated proliferative response, which might be of great interest not only in hematopoiesis, but also in other immunological processes, Alzheimer disease, alveolar proteinosis and wherever GM-CSF exerts its effects.


Assuntos
Gangliosídeos/farmacologia , Fator Estimulador de Colônias de Granulócitos e Macrófagos/farmacologia , Animais , Linhagem Celular , Membrana Celular/efeitos dos fármacos , Membrana Celular/metabolismo , Proliferação de Células/efeitos dos fármacos , Densitometria , Imunofluorescência , Gangliosídeo G(M3)/farmacologia , Gangliosídeos/biossíntese , Regulação da Expressão Gênica/efeitos dos fármacos , Camundongos , Microscopia Confocal , Morfolinas/farmacologia , Isoformas de Proteínas/genética , Isoformas de Proteínas/metabolismo , Receptores de Fator Estimulador das Colônias de Granulócitos e Macrófagos/genética , Receptores de Fator Estimulador das Colônias de Granulócitos e Macrófagos/metabolismo , Solubilidade/efeitos dos fármacos
3.
Liver Int ; 26(4): 477-85, 2006 May.
Artigo em Inglês | MEDLINE | ID: mdl-16629652

RESUMO

BACKGROUND/AIMS: Oxidative stress plays an important role in liver fibrosis. Under pathological conditions, hepatic stellate cells (HSC) undergo an activation process, developing a myofibroblast-like phenotype from the lipocyte phenotype. In this study, we determined the levels of oxidative stress and proliferation in different activation states of an experimental model of mouse HSC, the GRX cell line. These cells can be induced in vitro to display a more activated state or a quiescent phenotype. METHODS/RESULTS: We observed increased oxidative damage and higher levels of reactive oxygen species, measured by thiobarbituric acid reactive species and 2',7'-dichlorofluorescein diacetate, respectively, and diminished catalase activity in activated cells. Activation decreased proliferation and increased the number of cells in G2/M. Antioxidants N-acetylcysteine and Trolox varied in their capacity to correct the oxidative stress and proliferation status. CONCLUSIONS: The differences in physiological functions of stellate cell phenotypes suggest a relationship between oxidative stress levels and activation state.


Assuntos
Cirrose Hepática/fisiopatologia , Fígado/citologia , Fígado/fisiologia , Estresse Oxidativo/fisiologia , Acetilcisteína/farmacologia , Animais , Antioxidantes/farmacologia , Catalase/metabolismo , Linhagem Celular , Proliferação de Células/efeitos dos fármacos , Cromanos/farmacologia , Citocinas/farmacologia , Fígado/efeitos dos fármacos , Cirrose Hepática/patologia , Camundongos , Estresse Oxidativo/efeitos dos fármacos , Fenótipo , Espécies Reativas de Oxigênio/metabolismo , Fator de Necrose Tumoral alfa/farmacologia , Vitamina E/farmacologia
4.
Braz. j. med. biol. res ; 30(5): 591-7, May 1997. tab, graf
Artigo em Inglês | LILACS | ID: lil-196669

RESUMO

Follicle-stimulating hormone (FSH) and insulin regulate glycide metabolism in Sertoli cells, thus stimulating lactate production. These stimulatory effects of FSH and insulin do not require protein synthesis, suggesting a modulation of enzyme activity and/or regulation of glucose transport. The present investigation was performed to characterize the hormonal control of lipid metabolism in Sertoli cells. The data indicate that FSH and insulin have a regulatory effect on lipid metabolism in Sertoli cells. After 8 h of preincubation with insulin (5 mug/ml), the activity of the enzyme ATP-citrate lyase in sultured Sertoli cells was increased from 0.19 to 0.34 nmol NAD+ formed mug protein(-1) min(-1). FSH (100 ng/ml) had no effect on this enzyme. Glycerol phosphate dehydrogenase activity was not affected by any of the hormones tested. When Sertoli cells from 19-day old rats were incubated with [1,2-14C] acetate for 90 or 360 min, the [14C] label was present predominantly in triglyceride and phospholipid fractions with minor amounts in other lipids. In Sertoli cells pretreated for 16 h with insulin and FSH, an increase in acetate incorporation into lipids was observed. Most of the label was in esterified lipids and this percentage increased with the time of treatment; this increase was remarkable in triglycerides of control cells (18.8 percent to 30.6 percent). Since Sertoli cell triglycerides participate in the control of spermatogenesis, the present data suggest that the hormonal control of lipid metabolism in Sertoli cells is important not only for maintaining the energy of the cell itself, but also for the control of the spermatogenesis process.


Assuntos
Ratos , Masculino , Animais , Recém-Nascido , Acetatos/metabolismo , ATP Citrato (pro-S)-Liase/metabolismo , Hormônio Foliculoestimulante/metabolismo , Glicerolfosfato Desidrogenase/metabolismo , Insulina/metabolismo , Ácido Láctico/biossíntese , Lipídeos/biossíntese , Células de Sertoli/metabolismo , Técnicas de Cultura de Células , Glucose/metabolismo , Ratos Wistar
5.
Braz. j. med. biol. res ; 27(9): 2207-11, Sept. 1994. ilus, graf
Artigo em Inglês | LILACS | ID: lil-144474

RESUMO

In order to investigate the influence of biomatrix on Sertoli cell morphology and on the phospholipids content, these cells were isolated from tests of 15-day old Wistar rats and plated ontoplastic coated with extracellular matrix extracted froma seminiferous tubules, here denoted biomatix. When the Sertoli cells were cultured on biomatrix they did not from a monolayer until day 7 of culture, while cells plated onto plastic did so 48 h after plating. On day 5 of culture. Sertoli cells were incubated for 48 h with 5 µCi/ml 32P. There was no difference in 32P incorporation into lipids of cells plated onto biomatrix or plastic. However, there was a larger amount of phospholipid phosphate in cells plated onto biomatrix than onto plastic. When the phospholipds were analyzed by bidimensional thin-layer chromatography, no diferences were detected in their distribution; however, there was a significant decrease in the percentage of sphingomyelin in cells plated onto biomatrix when compared to plastic. These results showed that the cells cultured on biomatrix change their phospholipids content, but not their distribution. The importance of a small reduction in sphingomyelin content remains to be investigated


Assuntos
Ratos , Animais , Masculino , Células de Sertoli/química , Fosfolipídeos/análise , Autorradiografia , Células Cultivadas , Células de Sertoli/fisiologia , Cromatografia em Camada Fina , Meios de Cultura Livres de Soro , Matriz Extracelular/fisiologia , Plásticos , Ratos Wistar , Fatores de Tempo , Túbulos Seminíferos/citologia
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