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Esposito, V.

Publications and source records attributed to Esposito, V..

2 recordsLinked to original sources

Characterization of undocumented CO2 hydrothermal vents in the Mediterranean Sea: implications for ocean acidification studies

A previously undocumented shallow water hydrothermal field from Sicily (Southern Tyrrhenian Sea, Italy), is here described based on a multidisciplinary investigation. The field, covering an area of nearly 8000 m2 and ranging in depth from surface to -5 m, was explored in June 2021, to characterise the main physico-chemical features of the water column, describe bottom topography and features, and identify the main megabenthic and nektonic species. Twenty sites were investigated to characterize the carbonate system. Values of pH ranged between 7.84 and 8.04, {Omega}Ca between 3.68 and 5.24 and {Omega}Ar from 2.41 to 3.44. Geochemical analyses of hydrothermal fluids gases revealed a dominance of CO2 (98.1%) along with minor amounts of oxygen and reactive gases. Helium isotope ratios (R/Ra =2.51) and {delta}13CCO2 (3) support an inorganic origin of hydrothermal degassing of CO2 and the ascent of heat and deep-seated magmatic fluids to the surface. Visual census of fishes and megabenthos (mainly sessile organisms) allowed identification of 62 species, of which four are protected by the SPA/BIO Protocol and two by the International Union for Conservation of Nature. The macroalgae Halopteris scoparia and Jania rubens and the sponge Sarcotragus sp. were the dominant taxa in the area, while among fishes Coris julis and Chromis chromis were predominant. The preliminary description of this venting field indicates this site as an area of considerable interest and suitable for future experimental studies on ocean acidification.

ecology↗

Adipocyte differentiation of 3T3-L1 cells under TAF, TDF and INSTIs selective challenge: an in vitro model.

Integrase strand transfer inhibitors (INSTI) are a recently available class of antiretroviral therapy (ART) medications with a good tolerability profile and a high genetic barrier to HIV drug resistance. However, several studies report more significant weight gain among persons receiving INSTI-based ART regimens for initial therapy compared to protease inhibitors (PIs) and nucleoside reverse transcriptase inhibitors (NNRTI)-based regimens. In our experimental setting, we used the in vitro model of adipogenesis of 3T3-L1 cells to investigate the effects of the NRTIs tenofovir disoproxil fumarate (TDF) and tenofovir alafenamide (TAF), alone or in combination with four integrase strand transfer inhibitors: raltegravir (RAL), elvitegravir (ELV), dolutegravir (DTG) and bictegravir (BIC) on adipose differentiation. In addition, protein expression levels of PPAR{gamma} and C/EBP, and the intracellular lipid accumulation by Red Oil staining, were used to monitor adipocyte differentiation. Compared to control, RAL, ELV, DTG, and BIC were all able to increase adipogenesis, being in this, RAL and ELV more efficient. On the other hand, TAF and TDF inhibited adipogenesis. Moreover, when used in combination with the other INSTI molecules, TAF and TDF were able to reduce the adipogenic effects of all four drugs. This ability was more evident when TAF was used in combination with DTG and BIC. All these data suggest that TAF and TDF have an inhibitory effect on adipogenesis in vitro and that they could also effectively counteract the increased adipogenesis caused by the treatment with INSTIs. Finally, to evaluate if the 3T3-L1 cell could express fibroblast-like features following INSTIs treatment, we evaluated the immunohistochemical expression of ER-TR7, a well-known fibroblastic marker. This last assay showed that treatment with INSTIs increased the expression of ER-TR7 compared to control and to cells treated with TAF o TDF. In conclusion, our experimental data support the evidence that in vitro challenge of 3T3-L1 cells with INSTIs is able to increase adipocytic differentiation and to drive a number of these cells toward the expression of fibroblastic features, with a different degree according to the various drugs used, while TAF and TDF have an antagonistic role on this phenomenon.

pharmacology and toxicology↗