| Autor: |
Stokłosa P; Institute of Biochemistry and Molecular Medicine, University of Bern, 3012 Bern, Switzerland., Kappel S; Institute of Biochemistry and Molecular Medicine, University of Bern, 3012 Bern, Switzerland., Peinelt C; Institute of Biochemistry and Molecular Medicine, University of Bern, 3012 Bern, Switzerland. |
| Jazyk: |
angličtina |
| Zdroj: |
Cells [Cells] 2022 May 30; Vol. 11 (11). Date of Electronic Publication: 2022 May 30. |
| DOI: |
10.3390/cells11111793 |
| Abstrakt: |
Under physiological conditions, the widely expressed calcium-activated TRPM4 channel conducts sodium into cells. This sodium influx depolarizes the plasma membrane and reduces the driving force for calcium entry. The aberrant expression or function of TRPM4 has been reported in various diseases, including different types of cancer. TRPM4 is mainly localized in the plasma membrane, but it is also found in intracellular vesicles, which can undergo exocytosis. In this study, we show that calcium-induced exocytosis in the colorectal cancer cell line HCT116 is dependent on TRPM4. In addition, the findings from some studies of prostate cancer cell lines suggest a more general role of TRPM4 in calcium-induced exocytosis in cancer cells. Furthermore, calcium-induced exocytosis depends on TRPM4 ion conductivity. Additionally, an increase in intracellular calcium results in the delivery of TRPM4 to the plasma membrane. This process also depends on TRPM4 ion conductivity. TRPM4-dependent exocytosis and the delivery of TRPM4 to the plasma membrane are mediated by SNARE proteins. Finally, we provide evidence that calcium-induced exocytosis depends on TRPM4 ion conductivity, not within the plasma membrane, but rather in TRPM4-containing vesicles. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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