增长因子诱导的Ras和Rap1激活的时空图像
N Mochizuki1, S Yamashita, K Kurokawa
1Department of Structural Analysis, National Cardiovascular Center Research Institute, 5-7-1 Fujishirodai, Suita-shi, Osaka 565-8565, Japan.
Nature
|June 29, 2001
概括
这项研究可视化了使用光共振能量转移 (FRET) 传感器在细胞中的Ras和Rap1蛋白激活. 它揭示了细胞信号和分化至关重要的独特的空间激活模式.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 生物化学 生物化学
背景情况:
- 拉斯家族的G蛋白是细胞信号级联中的关键分子开关.
- 活细胞内Ras和Rap1激活的精确定位和时空动力学仍然在很大程度上没有特征.
研究的目的:
- 为了研究Ras和Rap1蛋白质的时空激活模式,以应对生长因子刺激.
- 阐明神经元细胞中持续Ras活动背后的机制.
主要方法:
- 利用基于光共振能量转移 (FRET) 的生物传感器实时可视化蛋白质激活.
- 在光漂白后使用光回收 (FRAP) 来评估蛋白质周转率.
主要成果:
- 表皮生长因子 (EGF) 诱导Ras的外周血激活和COS-1细胞中的Rap1的细胞内核激活.
- 神经生长因子 (NGF) 在PC12细胞的血中启动Ras激活,在细胞体中扩散并扩展神经元.
- 在神经细胞中持续的Ras活性归因于高的GTP/GDP交换率和/或低的GTPase活性,而不是蛋白质保留.
结论:
- 拉斯和Rap1表现出明显的亚细胞激活局部化,这可能解释了它们在细胞反应中的差异性作用.
- 这些发现提供了关于神经元细胞如何通过Ras信号动态来区分分化和生存的信号的见解.
更多相关视频
13:59A Quantitative Measurement of Reactive Oxygen Species and Senescence-associated Secretory Phenotype in Normal Human Fibroblasts During Oncogene-induced Senescence
Published on: August 12, 2018
7.5K
06:56Author Spotlight: Developing Tools to Tune the Activity of Tyrosine Phosphatases
Published on: September 6, 2024
856
相关概念视频
Abnormal Proliferation
4.0K
Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the...
4.0K
The Ras Gene
5.7K
The Ras-gene-encoded proteins are regulators of signaling pathways controlling cell proliferation, differentiation, or cell survival. The Ras-gene family in humans constitutes three primary members—the HRas, NRas, and KRas. These genes code for four functionally distinct yet closely related proteins—the HRas, NRas, KRas4A, and KRas4B. The involvement of mutant Ras genes in human cancer was first discovered in 1982 and is among the most common causes of human tumorigenesis.
Ras is a...
Ras is a...
5.7K
mTOR Signaling and Cancer Progression
3.6K
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...
3.6K
Small GTPases - Ras and Rho
4.4K
Ras and Rho are small monomeric GTPases that act downstream of receptor tyrosine kinase (RTK) and regulate various cellular processes. These GTPases switch between active and inactive states by binding to guanine nucleotides.
Three regulatory proteins control their activity:
Three regulatory proteins control their activity:
4.4K
MAPK Signaling Cascades
7.3K
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...
7.3K
PI3K/mTOR/AKT Signaling Pathway
5.1K
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...
5.1K
