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関連する概念動画

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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関連する実験動画

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+は,プラズマ膜のIP3受容体を通って侵入する.

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
まとめ

イノシトール1,4,5-トリスホスファート受容体 (IP3Rs) は,血膜に存在し,B細胞受容体シグナル伝達に不可欠なカルシウムイオン (Ca2+) の侵入を媒介する. 数少ないIP3RがCa2+流入に重大な影響を及ぼし,以前の理解に挑戦しています.

科学分野:

  • 細胞生物学 細胞生物学
  • 免疫学 免疫学とは
  • 分子生理学 分子生理学

背景:

  • イノシトール1,4,5-トリフォスファート受容体 (IP3Rs) は,主に細胞内貯蔵物から放出されるカルシウムイオン (Ca2+) を調節する.
  • プラズマ膜を通過するCa2+の侵入を媒介するIP3Rの役割は,まだ十分に理解されていません.

研究 の 目的:

  • 特にB細胞受容体 (BCR) アクティベーションに対する反応として,Ca2+エントリーにおけるIP3Rの機能を調査する.
  • プラズマ膜Ca2+透過性に対するIP3Rの局所と貢献を決定する.

主な方法:

  • DT40のニワトリとマウスのB細胞における全細胞および穿孔パッチクランプの電気生理学.
  • IP3R発現と毛孔機能の遺伝子操作.
  • サイト・ディレクテッド・ミュータジェネシスと機能的発現の研究.

主要な成果:

  • IP3Rの活性化は,プラズマ膜 (PM) にある少数のCa2+透過性チャネルを開く.
  • BCRの活性化も同様に,IP3R機能に依存するCa2+エントリを誘発します.
  • IP3RはPMで機能的に表現され,BCRによって誘発されるCa2+信号に大きく貢献します.

さらに関連する動画

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

関連する実験動画

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

結論:

  • IP3Rsは,エンドプラズマ網膜に加えて,プラズマ膜にユニークに局所されています.
  • PM IP3Rの少数の集団は,BCR媒介によるCa2+流入において重要な役割を果たしています.
  • これらの発見は,細胞カルシウムシグナル伝達と免疫応答におけるIP3Rの役割を再定義しています.