Cardiomyocyte S1PR1 promotes cardiac regeneration via AKT/mTORC1 signaling pathway DOI Creative Commons
Xiuxiang Liu, Jinnan Yue,

Caixia Zhou

и другие.

Theranostics, Год журнала: 2024, Номер 15(4), С. 1524 - 1551

Опубликована: Дек. 31, 2024

Aims: Lower vertebrates and some neonatal mammals are known to possess the ability regenerate cardiomyocyte fully recover after heart injuries within a limited period. Understanding molecular mechanisms of regeneration exploring new ways enhance cardiac hold significant promise for therapeutic intervention failure. Sphingosine 1-phospahte receptor 1 (S1PR1) is highly expressed in cardiomyocytes plays crucial role development pathological remodeling. However, effect cardiomyocyte-expressing S1PR1 on has not yet been elucidated. This study aims investigate following injuries. Methods Results: We generated (CM)-specific S1pr1 knock-out mice demonstrated that CM-specific loss-of-function severely reduced proliferation inhibited apex resection mice. Conversely, AAV9-mediated gain-of-function significantly enhanced regeneration. identified activated AKT/mTORC1/CYCLIN D1 BCL2 signaling pathways promote inhibit apoptosis. Moreover, CM-targeted gene delivery system via AAV9 overexpress increased improved functions myocardial infarction adult mice, suggesting potential method improve function injured heart. Conclusions: demonstrates CM-S1PR1 an essential research provides strategy by overexpression as

Язык: Английский

The sphinx helps to answer the riddle of cardiac regeneration DOI
Jae Woo Jung, Timothy Hla, Zoltàn Arany

и другие.

Trends in Endocrinology and Metabolism, Год журнала: 2024, Номер 35(8), С. 677 - 679

Опубликована: Май 16, 2024

Язык: Английский

Процитировано

0

Protocol to evaluate rat and mouse cardiomyocyte proliferation in vitro and in vivo DOI Creative Commons
Bin Li, Wei Yan, Yijie Guo

и другие.

STAR Protocols, Год журнала: 2024, Номер 5(3), С. 103204 - 103204

Опубликована: Июль 21, 2024

Here, we present a protocol for the quantitative assessment of rat and mouse cardiomyocyte proliferation both in vitro vivo. For vivo approach, describe steps isolation neonatal cardiomyocytes employment various indicators to quantify cell proliferation. We then detail procedures that incorporate comprehensive assays genetic lineage tracing strategy evaluate endogenous This can be modified investigate other mammalian complete details on use execution this protocol, please refer Ji et al.

Язык: Английский

Процитировано

0

Long non-coding RNAs-Sphingolipid Metabolism Nexus: Potential Targets for Cancer Treatment DOI Creative Commons
Yan Chen, J H Dai, Peng Chen

и другие.

Pharmacological Research, Год журнала: 2024, Номер unknown, С. 107539 - 107539

Опубликована: Дек. 1, 2024

Long non-coding RNAs (lncRNAs) have emerged as pivotal regulators of cancer pathogenesis, influencing various cellular processes and contributing to tumorigenesis. Sphingolipid metabolism has garnered interest a potential target for therapy owing its considerable diagnostic prognostic value. Recent studies demonstrated that lncRNAs regulate tumor-associated metabolic reprogramming via sphingolipid metabolism. However, the precise nature interactions between remains unclear. This review summarizes key roles in We emphasize interaction influences their impact on both prognosis drug resistance. These findings suggest lncRNA-sphingolipid holds great newl treatment.

Язык: Английский

Процитировано

0

Cardiomyocyte S1PR1 promotes cardiac regeneration via AKT/mTORC1 signaling pathway DOI Creative Commons
Xiuxiang Liu, Jinnan Yue,

Caixia Zhou

и другие.

Theranostics, Год журнала: 2024, Номер 15(4), С. 1524 - 1551

Опубликована: Дек. 31, 2024

Aims: Lower vertebrates and some neonatal mammals are known to possess the ability regenerate cardiomyocyte fully recover after heart injuries within a limited period. Understanding molecular mechanisms of regeneration exploring new ways enhance cardiac hold significant promise for therapeutic intervention failure. Sphingosine 1-phospahte receptor 1 (S1PR1) is highly expressed in cardiomyocytes plays crucial role development pathological remodeling. However, effect cardiomyocyte-expressing S1PR1 on has not yet been elucidated. This study aims investigate following injuries. Methods Results: We generated (CM)-specific S1pr1 knock-out mice demonstrated that CM-specific loss-of-function severely reduced proliferation inhibited apex resection mice. Conversely, AAV9-mediated gain-of-function significantly enhanced regeneration. identified activated AKT/mTORC1/CYCLIN D1 BCL2 signaling pathways promote inhibit apoptosis. Moreover, CM-targeted gene delivery system via AAV9 overexpress increased improved functions myocardial infarction adult mice, suggesting potential method improve function injured heart. Conclusions: demonstrates CM-S1PR1 an essential research provides strategy by overexpression as

Язык: Английский

Процитировано

0