依赖的直接反控制因诺西1,4,5-三酸盐诱导的Ca2+释放
Nature
|November 5, 1992
概括
信号传递对细胞至关重要. 这项研究表明,依赖的反机制控制了因诺西1,4,5-三酸盐 (InsP3) 诱导的释放,从而使细胞反应迅速和局部化.
科学领域:
- 细胞生物学 细胞生物学
- 生物化学 生物化学
- 身体生理学 身体生理学
背景情况:
- 细胞内 (Ca2+) 度动态对于细胞信号传导至关重要.
- 伊诺西1,4,5-三酸盐 (InsP3) 中介激素诱导的Ca2+释放,通常发生在突然和狭窄的细胞空间.
- 控制InsP3诱导的Ca2+释放动力学的精确机制仍然不完全理解.
研究的目的:
- 为了研究InsP3诱导的Ca2+释放的动力性质.
- 阐明依赖反在调节Ca2+释放的时间过程和特征中的作用.
- 探索积极合作和反控制对InsP3度-Ca2+释放关系的度的贡献.
主要方法:
- 使用 InsP3 和 Ca2+ 的闪光光电解来分析 Ca2+ 释放动力学.
- 实验操作探测反控制机制.
- 动力建模以支持观察到的现象.
主要成果:
- 证明了依赖Ca2+的即时反控制显著影响Ca2+释放的时间进程.
- 确定了这种积极反机制对于InsP3诱导的Ca2+释放的"负载依赖性"的重要性.
- 提供了在通道开放中积极合作的证据,反控制放大了的InsP3度-Ca2+释放关系.
结论:
- 对Ca2+依赖的反控制是InsP3诱导的Ca2+释放动力学的关键决定因素.
- 积极的合作和反机制有助于生成时间突然和空间有限的Ca2+信号.
- 这些发现提供了关于细胞信号传递的基本机制的见解.
相关概念视频
G-Protein Gated Ion Channels
GPCRs are primarily responsible for our sense of smell, taste, and vision. The binding of a sensory stimulus activates GPCR to stimulate effector proteins, many of which are ion channels in the sensory organs. GPCRs modulate the opening and closing of the target ion channels either directly by binding them, or by releasing second messengers that activate these channels. As ions move across the membrane, the membrane potential is altered, which induces an appropriate response.
Sensory organs,...
Sensory organs,...
IP3/DAG Signaling Pathway
Membrane lipids such as phosphatidylinositol (PI) are precursors for several membrane-bound and soluble second messengers. Specific kinases phosphorylate PI and produce phosphorylated inositol phospholipids. One such inositol phospholipids are the phosphatidylinositol-4,5 bisphosphate [PI(4,5)P2], present in the inner half of the lipid bilayer. Upon ligand binding, GPCR stimulates Gq proteins to turn on phospholipase Cꞵ. Activated phospholipase Cꞵ cleaves PI(4,5)P2 and produces two-second...
Feedback Regulation of Calcium Concentration
Calcium is an essential signaling molecule required for various cellular functions. Calcium pumps and ion channels on cell and organellar membranes, such as those on the endoplasmic reticulum (ER), regulate calcium concentrations inside the cell. They remain closed, keeping the cytosolic calcium levels low at a resting state.
Various transmembrane receptors, such as G protein-coupled receptors (GPCRs), elicit a response to extracellular signals by increasing cytosolic calcium. Activated GPCRs...
Various transmembrane receptors, such as G protein-coupled receptors (GPCRs), elicit a response to extracellular signals by increasing cytosolic calcium. Activated GPCRs...
Calmodulin-dependent Signaling
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,...
Ligand-Gated Ion Channel Receptor: Gating Mechanism
Ligand-gated ion channels are transmembrane proteins that play a vital role in intercellular communication and functions of the nervous system. They allow the influx of ions across the membrane once the neurotransmitter binds, allowing the subsequent transmission of electrical excitation across the neurons. Other ligand-gated ion channels, like the γ-aminobutyric acid (GABA) receptor, permit anions like chloride into the cells on the binding of the GABA molecule. Their entry into the cell...
Antihypertensive Drugs: Action of Calcium Channel Blockers
Calcium ions are essential to contract smooth muscle cells in blood vessels. They enter these cells through voltage-dependent calcium channels, specifically L-type calcium channels in the cell membrane. These L-type calcium channels are integral to the excitation-contraction coupling process in smooth muscle. When a stimulus is received by smooth muscle cells, their membrane depolarizes. This alteration in membrane potential instigates the opening of L-type calcium channels. As a result,...


