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衰老与细胞命运之间的联系:衰老相关分泌表型及其对干细胞命运转变的影响。

Link Between Senescence and Cell Fate: Senescence-Associated Secretory Phenotype and Its Effects on Stem Cell Fate Transition.

机构信息

Health Science Center, the 2nd Affiliated Hospital of Shenzhen University, Shenzhen University, Shenzhen, China.

Department of Dermatology, Shenzhen University General Hospital, Shenzhen, China.

出版信息

Rejuvenation Res. 2022 Aug;25(4):160-172. doi: 10.1089/rej.2022.0021. Epub 2022 Jul 28.


DOI:10.1089/rej.2022.0021
PMID:35658548
Abstract

Senescence is a form of durable cell cycle arrest elicited in response to a wide range of stimuli. Senescent cells remain metabolically active and secrete a variety of factors collectively termed senescence-associated secretory phenotype (SASP). SASP is highly pleiotropic and can impact numerous biological processes in which it has both beneficial and deleterious roles. The underlying mechanisms by which SASP exerts its pleiotropic influence remain largely unknown. SASP serves as an environmental factor, which regulates stem cell differentiation and alters its routine. The latter can potentially be accomplished through dedifferentiation, transdifferentiation, or reprogramming. Behavioral changes that cells undergo when exposed to SASP are involved in several senescence-associated physiological and pathological phenomena. These findings provide clues for identifying possible interventions to reduce the deleterious effects without interfering in the beneficial outcomes. In this study, we discuss the multifaceted effects of SASP and the changes occurring in cellular states upon exposure to SASP factors.

摘要

衰老是一种持久的细胞周期停滞形式,是对广泛刺激的反应。衰老细胞仍然具有代谢活性,并分泌各种因子,统称为衰老相关分泌表型(SASP)。SASP 具有高度的多效性,可以影响许多生物学过程,其中既有有益的作用,也有有害的作用。SASP 发挥其多效性影响的潜在机制在很大程度上尚不清楚。SASP 作为一种环境因素,调节干细胞分化并改变其常规。后者可能通过去分化、转分化或重编程来实现。细胞暴露于 SASP 时经历的行为变化涉及几种与衰老相关的生理和病理现象。这些发现为确定可能的干预措施提供了线索,以减少有害影响,而不干扰有益的结果。在这项研究中,我们讨论了 SASP 的多方面影响以及细胞暴露于 SASP 因子时发生的细胞状态变化。

相似文献

[1]
Link Between Senescence and Cell Fate: Senescence-Associated Secretory Phenotype and Its Effects on Stem Cell Fate Transition.

Rejuvenation Res. 2022-8

[2]
Dynamic and scalable assessment of the senescence-associated secretory phenotype (SASP).

Methods Cell Biol. 2024

[3]
Potential Regulators of the Senescence-Associated Secretory Phenotype During Senescence and Aging.

J Gerontol A Biol Sci Med Sci. 2022-11-21

[4]
The senescence-associated secretory phenotype induces cellular plasticity and tissue regeneration.

Genes Dev. 2017-1-15

[5]
Overcoming the senescence-associated secretory phenotype (SASP): a complex mechanism of resistance in the treatment of cancer.

Mol Oncol. 2021-12

[6]
Chromatin basis of the senescence-associated secretory phenotype.

Trends Cell Biol. 2022-6

[7]
Senescence in head and neck squamous cell carcinoma: relationship between senescence-associated secretory phenotype (SASP) mRNA expression level and clinicopathological features.

Clin Transl Oncol. 2024-4

[8]
Amphiregulin mediates non-cell-autonomous effect of senescence on reprogramming.

Cell Rep. 2022-7-12

[9]
The senescence-associated secretory phenotype in ovarian cancer dissemination.

Am J Physiol Cell Physiol. 2022-7-1

[10]
IFN-γ and TNF Induce Senescence and a Distinct Senescence-Associated Secretory Phenotype in Melanoma.

Cells. 2022-4-30

引用本文的文献

[1]
Exosomes derived from umbilical cord mesenchymal stem cells alleviate jaw bone marrow mesenchymal stem cells senescence and restore osteogenic differentiation potential.

Stem Cell Res Ther. 2025-8-29

[2]
Comprehensive analysis of PRPF19 immune infiltrates, DNA methylation, senescence-associated secretory phenotype and ceRNA network in bladder cancer.

Front Immunol. 2023

[3]
PDK4-dependent hypercatabolism and lactate production of senescent cells promotes cancer malignancy.

Nat Metab. 2023-11

[4]
Non-Genomic Hallmarks of Aging-The Review.

Int J Mol Sci. 2023-10-23

[5]
Cancer Bioenergetics and Tumor Microenvironments-Enhancing Chemotherapeutics and Targeting Resistant Niches through Nanosystems.

Cancers (Basel). 2023-7-28

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