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Splicing factor SRSF1 attenuates cardiomyocytes apoptosis via regulating alternative splicing of Bcl2L12.

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November 2024

Zhuhai People's Hospital (Zhuhai Clinical Medical College of Jinan University), Guangdong Provincial Key Laboratory of Tumor Interventional Diagnosis and Treatment, Jinan University, Zhuhai, 519000, Guangdong, China.

Background: Aberrant alternative splicing (AS) events, triggered by the alterations in serine/arginine splicing factor 1 (SRSF1), a member of the SR protein family, have been implicated in various pathological processes. However, the function and mechanism of SRSF1 in cardiovascular diseases remain unclear.

Results: In this study, we found that the expression of SRSF1 was significantly down-regulated in the hearts of mice with acute myocardial infarction (AMI) and H9C2 cells exposed to HO.

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Bcl2l12, a novel protein interacting with Arf6, triggers Schwann cell differentiation programme.

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Laboratory of Molecular Neurology, Department of Life Sciences, 1432-1 Horinouchi, Hachioji, Tokyo University of Pharmacy and Life Sciences, Tokyo 192-0392, Japan.

Schwann cells are glial cells in the peripheral nervous system (PNS); they wrap neuronal axons with their differentiated plasma membranes called myelin sheaths. Although the physiological functions, such as generating saltatory conduction, have been well studied in the PNS, the molecular mechanisms by which Schwann cells undergo their differentiation programme without apparent morphological changes before dynamic myelin sheath formation remain unclear. Here, for the first time, we report that Arf6, a small GTP/GDP-binding protein controlling morphological differentiation, and the guanine-nucleotide exchange factors cytohesin proteins are involved in the regulation of Schwann cell differentiation marker expression in primary Schwann cells.

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  • BSN-37 is a novel antimicrobial peptide isolated from bovine spleen that shows antibacterial and immunomodulatory properties, prompting a study on its effects on mouse macrophages RAW264.7.
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