亡信号调节激酶1促进衰老和衰老中的炎症
Takeru Odawara1, Shota Yamauchi2, Hidenori Ichijo3,4
1Laboratory of Cell Signaling, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
Communications biology
|June 5, 2024
概括
亡信号调节激酶1 (ASK1) 驱动细胞衰老和衰老中的炎症. 抑制ASK1可能为与年龄相关的疾病和癌症提供治疗点.
科学领域:
- 细胞和分子生物学 细胞和分子生物学
- 免疫学 免疫学 免疫学
- 衰老研究研究 衰老研究
背景情况:
- 细胞衰老是一种永久性细胞循环停止的状态.
- 衰老细胞通过与衰老相关的分泌表型 (SASP) 释放促炎因素.
- SASP有助于慢性炎症和衰老,但其调节不清楚.
研究的目的:
- 研究亡信号调节激酶1 (ASK1) 在调节SASP中的作用.
- 确定ASK1在衰老,衰老和与年龄相关的疾病中的参与.
主要方法:
- 研究了老化细胞中的ASK1激活.
- 使用ASK1缺乏的小鼠来评估其体内功能.
- 分析了细胞因子和化学因子的表达.
- 评估瘤抑制和与年龄相关的病理学.
主要成果:
- ASK1在衰老过程中被激活,并通过激活p38激酶来促进SASP.
- 缺少ASK1会影响衰老细胞的清除,并增加瘤的发展.
- 缺少ASK1可以预防与年龄相关的炎症和血球硬化.
结论:
- ASK1是SASP的关键调节者,在衰老和衰老中促进炎症.
- ASK1对于瘤抑制和预防与年龄相关的疾病至关重要.
- ASK1代表了与年龄有关的疾病的潜在治疗标.
相关概念视频
The Extrinsic Apoptotic Pathway
6.3K
The extrinsic apoptotic pathway is initiated when extracellular death-inducing signals, such as specific cytokines, activate the death receptors expressed on the cell surface. The immune cells involved in this pathway are natural killer cells (NK cells) and cytotoxic T-lymphocytes. NK cells are critical in innate immune response, while cytotoxic T-lymphocytes are associated with adaptive immune response. These cells recognize specific receptors expressed on the altered cells and activate...
6.3K
PI3K/mTOR/AKT Signaling Pathway
3.5K
The mammalian target of rapamycin (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1 (mTORC1) and mTOR complex 2 (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast, mTORC2 consists of a...
3.5K
Apoptosis
11.4K
Apoptosis is a combination of two Greek words, 'apo' and 'ptosis,' meaning separation and falling off, respectively. Hippocrates used this word to describe gangrene, which was caused due to bandaging of fractured bones. Apoptosis was distinguished from necrosis in 1970 when John Kerr reported observations of morphological changes occurring during apoptosis. During one experiment, he observed that the disruption of blood supply to the liver tissue resulted in a size...
11.4K
mTOR Signaling and Cancer Progression
3.8K
The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
The mTOR pathway or the...
3.8K
The Intrinsic Apoptotic Pathway
6.5K
Internal cellular stress, such as cellular injury or hypoxia, triggers intrinsic apoptosis. The B-cell lymphoma 2 (Bcl-2) family of proteins are the primary regulators of the intrinsic apoptotic pathway. For example, during DNA damage, checkpoint proteins, such as Ataxia Telangiectasia Mutated (ATM protein) and Checkpoints Factor-2 (Chk2) proteins, are activated. These proteins phosphorylate p53 which further activates pro-apoptotic proteins, such as Bax, Bak, PUMA, and Noxa, and inhibits...
6.5K
Caspases
12.4K
Caspase, a family of cysteine proteases, serve as effectors in apoptosis. The ced3 gene in C.elegans was first identified to be involved in apoptosis. This gene encodes the ced-3 caspase that is similar to the interleukin-1-beta converting enzyme or ICE in mammals. In addition to apoptosis, caspases also function in the inflammatory response. Inflammatory caspases are essential in activating pro-inflammatory cytokines that recruit immune cells and block the replication of pathogens inside...
12.4K


