TRPM7通过准细胞内信号传递来控制皮肤角质细胞衰老
Xingjie Ma1, Dandan Qi2, Xiaoming Sun1,3
1Laboratory of Intensive Care, Department of Intensive Care, The Affiliated Hospital of Yangzhou University, Yangzhou University, China.
The FEBS journal
|August 26, 2024
概括
在皮肤衰老过程中,过渡性受体潜在的 Melastatin 7 (TRPM7) 通道升高,通过信号传递驱动角质细胞衰老. 这一发现提供了新的抗皮肤衰老治疗策略.
科学领域:
- 细胞生物学 细胞生物学
- 皮肤病学 皮肤病学
- 衰老研究研究 衰老研究
背景情况:
- 细胞衰老,一个不可逆转的细胞循环停止,驱动皮肤衰老和病理.
- 皮肤细胞衰老的机制和有效的抗衰老策略仍未得到充分探索.
- 细胞内信号传递是细胞衰老和衰老的关键调节者.
研究的目的:
- 为了研究相关因素在皮肤细胞衰老中的作用.
- 为抗皮肤衰老疗法确定新的分子标.
主要方法:
- 在衰老的皮肤角质细胞中分析了短暂受体潜力melastatin 7 (TRPM7) 的表达.
- 研究TRPM7对细胞内信号通路的影响.
- 评估TRPM7介导的失调对线粒体功能和DNA损伤的影响.
主要成果:
- 在衰老和老化的皮肤角质细胞中,TRPM7的表达显著升高.
- 通过促进转移到线粒体,TRPM7促进了角质细胞衰老.
- 线粒体过载会导致线粒体功能障碍,反应性氧物种的产生和DNA损伤.
结论:
- 通过细胞内信号传递,TRPM7作为皮肤角质细胞衰老的关键调节者.
- 针对TRPM7提供了一种有前途的治疗途径,用于对抗皮肤衰老.
相关概念视频
Renewal of Skin Epidermal Stem Cells
2.5K
The skin is divided into epidermis, dermis, and hypodermis, the skin's outermost, middle, and inner layers. The human epidermal layer regularly undergoes renewal, where old, dead cells are replaced by new cells. Epidermal stem cells or EpiSCs divide and differentiate to restore the lost cells. For the renewal process, some EpiSCs continuously self-renew. In contrast, few others differentiate into transit-amplifying cells, which later form prickle or spinous cells, followed by granular...
2.5K
Calmodulin-dependent Signaling
5.1K
Calmodulin (CaM) is a calcium-binding protein in eukaryotes that controls various calcium-regulated cellular processes. It has four calcium-binding sites that bind calcium to form the calcium-calmodulin ( Ca2+-CaM) complex. GPCR stimulation increases the calcium levels in the cells that bind to CaM and induces a conformational change.
The Ca2+-CaM complex does not have enzymatic activity by itself. Instead, the complex binds downstream target proteins, including membrane proteins or enzymes,...
The Ca2+-CaM complex does not have enzymatic activity by itself. Instead, the complex binds downstream target proteins, including membrane proteins or enzymes,...
5.1K
MAPK Signaling Cascades
5.3K
Mitogen-activated protein kinase, or MAPK pathway, activates three sequential kinases to regulate cellular responses such as proliferation, differentiation, survival, and apoptosis. The canonical MAPK pathway starts with a mitogen or growth factor binding to an RTK. The activated RTKs stimulate Ras, which recruits Raf or MAP3 Kinase (MAPKKK), the first kinase of the MAPK signaling cascade. Raf further phosphorylates and activates MEK or MAP2 Kinases (MAPKK), which in turn phosphorylates MAP...
5.3K
Mechanically-gated Ion Channels
6.3K
Mechanically-gated ion channels are proteins found in eukaryotic and prokaryotic cell membranes that open in response to mechanical stress. Tension, compression, swelling, and shear stress can alter the conformation of the protein, opening a transmembrane channel that allows the passage of ions for signal transmission. In eukaryotes, mechanically-gated channels are distributed in several regions like the neurons, lungs, skin, bladder, and heart, where they play critical roles in numerous...
6.3K
Enzyme-linked Receptors
77.7K
Enzyme-linked receptors are proteins that act as both receptor and enzyme, activating multiple intracellular signals. This is a large group of receptors that include the receptor tyrosine kinase (RTK) family. Many growth factors and hormones bind to and activate the RTKs.
Neurotrophin (NT) receptors are a family of RTKs, including trkA, trkB, and trkC (tropomyosin-related kinase) receptors. TrkA is specific for nerve growth factor (NGF), neurotrophin-6, and neurotrophin-7. TrkB binds...
Neurotrophin (NT) receptors are a family of RTKs, including trkA, trkB, and trkC (tropomyosin-related kinase) receptors. TrkA is specific for nerve growth factor (NGF), neurotrophin-6, and neurotrophin-7. TrkB binds...
77.7K
The Intrinsic Apoptotic Pathway
6.4K
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...
6.4K


