Role of cytosolic and endoplasmic reticulum Ca 2+ in pancreatic beta-cells: pros and cons.
Seung-Eun SongSu-Kyung ShinHyeon Yeong JuSeung-Soon ImDae-Kyu SongPublished in: Pflugers Archiv : European journal of physiology (2023)
Pancreatic beta cells utilize Ca 2+ to secrete insulin in response to glucose. The glucose-dependent increase in cytosolic Ca 2+ concentration ([Ca 2+ ] C ) activates a series of insulin secretory machinery in pancreatic beta cells. Therefore, the amount of insulin secreted in response to glucose is determined in a [Ca 2+ ] C -dependent manner, at least within a moderate range. However, the demand for insulin secretion may surpass the capability of beta cells. Abnormal elevation of [Ca 2+ ] C levels beyond the beta-cell endurance capacity can damage them by inducing endoplasmic reticulum (ER) stress and cell death programs such as apoptosis. Therefore, while Ca 2+ is essential for the insulin secretory functions of beta cells, it could affect their survival at pathologically higher levels. Because an increase in beta-cell [Ca 2+ ] C is inevitable under certain hazardous conditions, understanding the regulatory mechanism for [Ca 2+ ] C is important. Therefore, this review discusses beta-cell function, survival, ER stress, and apoptosis associated with intracellular and ER Ca 2+ homeostasis.
Keyphrases
- cell cycle arrest
- cell death
- induced apoptosis
- type diabetes
- endoplasmic reticulum
- endoplasmic reticulum stress
- oxidative stress
- protein kinase
- pi k akt
- signaling pathway
- public health
- single cell
- high intensity
- blood glucose
- glycemic control
- bone marrow
- cell therapy
- transcription factor
- adipose tissue
- reactive oxygen species