Mitochondria modulate ameloblast Ca 2+ signaling.

Autor: Costiniti V; Department of Molecular Pathobiology, New York University College of Dentistry, New York, New York, USA., Bomfim GHS; Department of Molecular Pathobiology, New York University College of Dentistry, New York, New York, USA., Neginskaya M; Department of Molecular Pathobiology, New York University College of Dentistry, New York, New York, USA., Son GY; Department of Molecular Pathobiology, New York University College of Dentistry, New York, New York, USA., Mitaishvili E; Department of Molecular Pathobiology, New York University College of Dentistry, New York, New York, USA., Giacomello M; Department of Biology, University of Padova, Padua, Italy.; Department of Biomedical Sciences, University of Padova, Padua, Italy., Pavlov E; Department of Molecular Pathobiology, New York University College of Dentistry, New York, New York, USA., Lacruz RS; Department of Molecular Pathobiology, New York University College of Dentistry, New York, New York, USA.
Jazyk: angličtina
Zdroj: FASEB journal : official publication of the Federation of American Societies for Experimental Biology [FASEB J] 2022 Feb; Vol. 36 (2), pp. e22169.
DOI: 10.1096/fj.202100602R
Abstrakt: The role of mitochondria in enamel, the most mineralized tissue in the body, is poorly defined. Enamel is formed by ameloblast cells in two main sequential stages known as secretory and maturation. Defining the physiological features of each stage is essential to understand mineralization. Here, we analyzed functional features of mitochondria in rat primary secretory and maturation-stage ameloblasts focusing on their role in Ca 2+ signaling. Quantification of the Ca 2+ stored in the mitochondria by trifluoromethoxy carbonylcyanide phenylhydrazone stimulation was comparable in both stages. The release of endoplasmic reticulum Ca 2+ pools by adenosine triphosphate in rhod2AM-loaded cells showed similar mitochondrial Ca 2+ ( m Ca 2+ ) uptake. However, m Ca 2+ extrusion via Na + -Li + -Ca 2+ exchanger was more prominent in maturation. To address if m Ca 2+ uptake via the mitochondrial Ca 2+ uniporter (MCU) played a role in cytosolic Ca 2+ ( c Ca 2+ ) buffering, we stimulated Ca 2+ influx via the store-operated Ca 2+ entry (SOCE) and blocked MCU with the inhibitor Ru265. This inhibitor was first tested using the enamel cell line LS8 cells. Ru265 prevented c Ca 2+ clearance in permeabilized LS8 cells like ruthenium red, and it did not affect ΔΨm in intact cells. In primary ameloblasts, SOCE stimulation elicited a significantly higher m Ca 2+ uptake in maturation ameloblasts. The uptake of Ca 2+ into the mitochondria was dramatically decreased in the presence of Ru265. Combined, these results suggest an increased mitochondrial Ca 2+ handling in maturation but only upon stimulation of Ca 2+ influx via SOCE. These functional studies provide insights not only on the role of mitochondria in ameloblast Ca 2+ physiology, but also advance the concept that SOCE and m Ca 2+ uptake are complementary processes in biological mineralization.
(© 2022 Federation of American Societies for Experimental Biology.)
Databáze: MEDLINE
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