Role of Ca2+ and ion channels in the regulation of apoptosis under hypoxia

• Autores: Miaohong Wang, Jin Tan, Yuyang Miao, Mengmeng Li, Qiang Zhang
• Localización: Histology and histopathology: cellular and molecular biology, ISSN-e 1699-5848, ISSN 0213-3911, Vol. 33, Nº. 3, 2018, págs. 237-246
• Idioma: inglés
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• Resumen

  • Hypoxia is a kind of common pathological condition existing in various diseases such as sleep apnea syndrome, myocardial infarction and stroke, which can precipitate the onset of diseases through inducing cell apoptosis. Ca2+ is the ubiquitous message in cell. Given the crucial role of Ca2+ in physiology, intracellular Ca2+ overload is a significant regulator of apoptosis. Numerous experiments show that hypoxia may cause changes of multiple cellular Ca2+ channels, for instance, Na+/Ca2+ Exchanger (NCX), L-type voltage dependent Ca2+ channel (L-VDCC), inositol triphosphate receptors (IP3R) and so on, which contribute to intracellular Ca2+ overload, thus eventually triggering cell apoptosis. However, the mechanisms underlying different Ca2+ channels involved in hypoxic apoptosis are complex. For example, chronic hypoxia or acute hypoxia may select different Ca2+ channels to influence cell apoptosis. In addition, intracellular Ca2+ overload may initiate different apoptotic pathways due to hypoxic duration. Furthermore, different locations in the cell of specific Ca2+ channels activated by hypoxia will determine different apoptosis signaling pathways. Moreover, activation of different Ca2+ channel isoforms will result in different outcomes of the cell under hypoxia. Hence, we aim to highlight the potential mechanisms of the main Ca2+ channels in regulation of apoptosis under hypoxic stress.