SIRT1:调节肺部疾病的关键途径的中间体
Yi-Zhu Jiang1, Xin-Ran Huang1, Jing Chang1
1Xiangya Nursing School, Central South University, Changsha, China; Department of Physiology, School of Basic Medical Science, Central South University, Changsha, Hunan, China.
概括
无声信息调节器类型-1 (SIRT1) 在肺部疾病中起着关键作用. 本综述详细介绍了SIRT1的情况.
科学领域:
- 分子生物学分子生物学
- 肺部病理学 肺部病理学
- 生物化学 生物化学
背景情况:
- 沉默信息调节器类型-1 (SIRT1) 是sirtuin家族中的一个NAD+依赖的脱乙酶.
- SIRT1表现出独特的蛋白脱乙酶活性,影响许多生理和病理生理过程.
- 它通过修改广泛的蛋白质基质和信号通路来发挥作用.
研究的目的:
- 审查了解SIRT1在肺部疾病中的作用的最新进展.
- 介绍有关SIRT1.1的基本信息.
- 总结一下SIRT1在各种肺部疾病中的重要参与.
主要方法:
- 最近科学出版物的文献综述.
- 综合现有关于SIRT1和肺部疾病的研究.
- 在不同肺病理中SIRT1功能的分类.
主要成果:
- SIRT1与急性肺损伤和急性呼吸困扰综合征有关.
- 该审查强调了SIRT1在慢性阻塞性肺病中的突出作用.
- 还讨论了SIRT1在肺癌和与衰老相关的肺部疾病中的参与.
结论:
- SIRT1是多种肺部疾病的发病和进展的关键因素.
- 对SIRT1调节的进一步研究可能为肺部疾病提供治疗策略.
- 了解SIRT1的机制对于解决肺部疾病至关重要,包括与衰老相关的肺部疾病.
相关概念视频
Interactions Between Signaling Pathways
6.3K
Signaling cascades usually lack linearity. Multiple pathways interact and regulate one another, allowing cells to integrate and respond to diverse environmental stimuli.
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
6.3K
The JAK-STAT Signaling Pathway
8.9K
Several cytokine receptors have tightly bound Janus kinase or JAK proteins attached at their cytosolic tail. Small signaling molecules such as cytokines, growth hormones, or prolactins bind to the cytokine receptors and initiate their dimerization. The dimerization brings the cytosolic JAKs together that trans-phosphorylate and activates each other. The activated JAKs now phosphorylate cytosolic tails of the cytokine receptors, which serve as binding sites for adaptor proteins such as SH2...
8.9K
NF-κB-dependent Signaling Pathway
7.4K
The transcription factor NF-κB was discovered in 1986 in the lab of Nobel laureate Professor David Baltimore, for its interaction with the immunoglobulin light chain enhancer in B-cells. After more than three decades of study, it is now evident that NF-κB regulates the expression of over 100 genes. Most of these genes play an essential role in the innate and adaptive immune responses as well as the inflammatory responses of animals.
NF-κB-dependent Signaling Mechanism
The...
NF-κB-dependent Signaling Mechanism
The...
7.4K
PI3K/mTOR/AKT Signaling Pathway
3.6K
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...
3.6K
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
Chronic Obstructive Pulmonary Disease-II: Pathophysiology
2.8K
Chronic Obstructive Pulmonary Disease (COPD) pathophysiology is intricate and multifaceted, involving a complex interplay of physiological processes. Understanding these mechanisms is crucial for effectively managing and treating COPD. Here is an in-depth look at the critical elements in the pathophysiology of COPD:
Chronic Inflammation
Chronic Inflammation
2.8K


