Gravity plays a key role in regulating cell processes such as proliferation, differentiation and cell function. The aim of the study was to evaluate the effects of microgravity on differentiation and exo-metabolome profile of human hepatic and biliary tree stem/progenitor cells. Simulated weightless conditions were obtained by the RCCS (Synthecon). Primary cultures of human biliary tree stem cells (hBTSCs) and immortalized human hepatic cell line (HepG2) were cultured in microgravity or in normogravity conditions. Self-replication and differentiation toward mature cells were determined, respectively, by culturing in Kubota’s Medium and hormonally defined medium tailored for hepatocyte differentiation. RT-qPCR was used to evaluate gene expression and NMR to analyze the cell exo-metabolome profile. Microgravity determined an increase of stemness genes (OCT4, SOX17, PDX1) in hBTSCs (p < 0.05 vs normogravity). hBTSCs cultured in microgravity showed an impaired capacity to differentiate toward mature hepatocytes, since the expression of hepatocyte lineage genes (ALB, ASBT and CYP3A4) was significantly lower with respect to normogravity (p < 0.05). In HepG2, the microgravity caused a lower (p < 0.05 vs normogravity) expression of CYP3A4, a terminal differentiation gene expressed in lobular zone 3. The NMR PCA of the exo-metabolome cell profile evidenced that, in microgravity, both cell lines presented higher glucose consumption and lower consumption of pyruvate and glutamate with respect to normogravity (p < 0.05), with formation of fermentation and ketogenesis products. Interestingly, while in normogravity the differentiation of hBTSCs toward mature hepatocytes was associated with increased oxidative phosphorylation (p < 0.05), this was prevented by microgravity in association with the impaired cell differentiation. Our results demonstrated significant combined biologic and metabolomic effects of microgravity on hepatic stem/progenitor cells with several implications. From one side, these effects of microgravity should be taken into consideration for space medicine programs but, from the other side, they could be interesting for the generation of devices based on stem/progenitor cells.

Microgravity maintains stemness and enhance glycolytic metabolism in human hepatic and biliary tree stem/progenitor cells / Costantini, Daniele; Cardinale, Vincenzo; Casadei, Luca; Carpino, G.; Nevi, Lorenzo; DI MATTEO, Sabina; Lustri, ANNA MARIA; Safarikia, Samira; Melandro, Fabio; Berloco, Pasquale Bartolomeo; Manetti, Cesare; Alvaro, Domenico. - 49:1(2017), pp. e14-e14. (Intervento presentato al convegno 24th National Congress of Digestive Diseases: Italian Federation of Societies of Digestive Diseases - FISMAD tenutosi a Rome) [10.1016/j.dld.2017.01.030].

Microgravity maintains stemness and enhance glycolytic metabolism in human hepatic and biliary tree stem/progenitor cells

COSTANTINI, DANIELE;CARDINALE, VINCENZO;CASADEI, LUCA;Carpino, G.;NEVI, LORENZO;DI MATTEO, SABINA;LUSTRI, ANNA MARIA;SAFARIKIA, Samira;MELANDRO, FABIO;BERLOCO, Pasquale Bartolomeo;MANETTI, Cesare;ALVARO, Domenico
2017

Abstract

Gravity plays a key role in regulating cell processes such as proliferation, differentiation and cell function. The aim of the study was to evaluate the effects of microgravity on differentiation and exo-metabolome profile of human hepatic and biliary tree stem/progenitor cells. Simulated weightless conditions were obtained by the RCCS (Synthecon). Primary cultures of human biliary tree stem cells (hBTSCs) and immortalized human hepatic cell line (HepG2) were cultured in microgravity or in normogravity conditions. Self-replication and differentiation toward mature cells were determined, respectively, by culturing in Kubota’s Medium and hormonally defined medium tailored for hepatocyte differentiation. RT-qPCR was used to evaluate gene expression and NMR to analyze the cell exo-metabolome profile. Microgravity determined an increase of stemness genes (OCT4, SOX17, PDX1) in hBTSCs (p < 0.05 vs normogravity). hBTSCs cultured in microgravity showed an impaired capacity to differentiate toward mature hepatocytes, since the expression of hepatocyte lineage genes (ALB, ASBT and CYP3A4) was significantly lower with respect to normogravity (p < 0.05). In HepG2, the microgravity caused a lower (p < 0.05 vs normogravity) expression of CYP3A4, a terminal differentiation gene expressed in lobular zone 3. The NMR PCA of the exo-metabolome cell profile evidenced that, in microgravity, both cell lines presented higher glucose consumption and lower consumption of pyruvate and glutamate with respect to normogravity (p < 0.05), with formation of fermentation and ketogenesis products. Interestingly, while in normogravity the differentiation of hBTSCs toward mature hepatocytes was associated with increased oxidative phosphorylation (p < 0.05), this was prevented by microgravity in association with the impaired cell differentiation. Our results demonstrated significant combined biologic and metabolomic effects of microgravity on hepatic stem/progenitor cells with several implications. From one side, these effects of microgravity should be taken into consideration for space medicine programs but, from the other side, they could be interesting for the generation of devices based on stem/progenitor cells.
2017
24th National Congress of Digestive Diseases: Italian Federation of Societies of Digestive Diseases - FISMAD
04 Pubblicazione in atti di convegno::04d Abstract in atti di convegno
Microgravity maintains stemness and enhance glycolytic metabolism in human hepatic and biliary tree stem/progenitor cells / Costantini, Daniele; Cardinale, Vincenzo; Casadei, Luca; Carpino, G.; Nevi, Lorenzo; DI MATTEO, Sabina; Lustri, ANNA MARIA; Safarikia, Samira; Melandro, Fabio; Berloco, Pasquale Bartolomeo; Manetti, Cesare; Alvaro, Domenico. - 49:1(2017), pp. e14-e14. (Intervento presentato al convegno 24th National Congress of Digestive Diseases: Italian Federation of Societies of Digestive Diseases - FISMAD tenutosi a Rome) [10.1016/j.dld.2017.01.030].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/956448
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