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相关概念视频

What are Second Messengers?01:12

What are Second Messengers?

Because many receptor binding ligands are hydrophilic, they do not cross the cell membrane and thus their message must be relayed to a second messenger on the inside. There are several second messenger pathways, each with their own way of relaying information. G-protein coupled receptors can activate both phosphoinositol and cyclic AMP (cAMP) second messenger pathways. The phosphoinositol path is active when the receptor induces phospholipase C to hydrolyze the phospholipid,...
Cell-surface Signaling01:21

Cell-surface Signaling

Hormones—or any molecule that binds to a receptor, known as a ligand—that are lipid-insoluble (water-soluble) are not able to diffuse across the cell membrane. In order to be able to affect a cell without entering it, these hormones bind to receptors on the cell membrane. When a first messenger, a hormone, binds to a receptor, a signal cascade is set off, causing second messengers, proteins inside the cell, to become activated, resulting in downstream effects.
Phosphoinositides and PIPs01:42

Phosphoinositides and PIPs

Phosphoinositides are a group of phospholipids containing a glycerol backbone with two fatty acid chains and a phosphate attached to a myoinositol sugar ring. The inositol head group extends into the cytoplasm, where it is modified by adding phosphate groups to form phosphatidylinositol phosphates or PIPs.
Different phosphoinositides are synthesized and recruited on the cytosolic face of the plasma membrane. The localization of specific phosphoinositides concentrated in separate membrane...
IP3/DAG Signaling Pathway01:11

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 Concentration01:27

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...
Calmodulin-dependent Signaling01:16

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,...

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相关实验视频

Updated: Jul 13, 2026

Direct Imaging of ER Calcium with Targeted-Esterase Induced Dye Loading (TED)
09:32

Direct Imaging of ER Calcium with Targeted-Esterase Induced Dye Loading (TED)

Published on: May 7, 2013

Ca2+通过血IP3受体进入体内.

Olivier Dellis1, Skarlatos G Dedos, Stephen C Tovey

  • 1Department of Pharmacology, Tennis Court Road, Cambridge, CB2 1PD, UK.

Science (New York, N.Y.)
|July 15, 2006
PubMed
概括

伊诺西1,4,5-三酸盐受体 (IP3R) 位于血膜上,介导离子 (Ca2+) 进入,对于B细胞受体信号传递至关重要. 很少有IP3R显著影响Ca2+流入,挑战以前的理解.

科学领域:

  • 细胞生物学 细胞生物学
  • 免疫学 免疫学 免疫学
  • 分子生理学分子生理学

背景情况:

  • 伊诺西1,4,5-三酸盐受体 (IP3Rs) 主要调节从细胞内储存的离子 (Ca2+) 释放.
  • 对于IP3Rs在调解Ca2+穿过等离子体膜的作用仍然不太清楚.

研究的目的:

  • 研究IP3Rs在Ca2+进入中的功能,特别是在响应B细胞受体 (BCR) 激活时.
  • 确定IP3Rs对血Ca2+透性的定位和贡献.

主要方法:

  • 在DT40和小鼠B细胞中,全细胞和穿孔贴片的电生理学.
  • 对IP3R表达和毛孔功能进行基因操纵.
  • 位点定向的突变发生和功能表达研究.

主要成果:

  • 通过IP3R激活,在血膜 (PM) 上打开了少量的Ca2+透通道.
  • 同样地,BCR激活也会引起依赖IP3R功能的Ca2+输入.
  • IP3Rs在PM上得到功能表达,对BCR引起的Ca2+信号有显著的贡献.

结论:

  • IP3Rs除了在细胞内膜外,还在血膜中具有独特的局部化.

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Targeting Cysteine Thiols for in Vitro Site-specific Glycosylation of Recombinant Proteins

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相关实验视频

Last Updated: Jul 13, 2026

Direct Imaging of ER Calcium with Targeted-Esterase Induced Dye Loading (TED)
09:32

Direct Imaging of ER Calcium with Targeted-Esterase Induced Dye Loading (TED)

Published on: May 7, 2013

Imaging Local Ca2+ Signals in Cultured Mammalian Cells
09:30

Imaging Local Ca2+ Signals in Cultured Mammalian Cells

Published on: March 3, 2015

Targeting Cysteine Thiols for in Vitro Site-specific Glycosylation of Recombinant Proteins
11:25

Targeting Cysteine Thiols for in Vitro Site-specific Glycosylation of Recombinant Proteins

Published on: October 4, 2017

  • 一个小数量的PM IP3Rs在BCR介导的Ca2+流入中发挥着关键作用.
  • 这些发现重新定义了IP3Rs在细胞信号传递和免疫反应中的作用.