In smooth muscle, FK506-binding protein modulates IP3 receptor-evoked Ca2+ release by mTOR and calcineurin

Debbi MacMillan1, Susan Currie, Karen N Bradley

  • 1Institute of Biomedical and Life Sciences, Neuroscience and Biomedical Systems, West Medical Building, University of Glasgow, Glasgow, G12 8QQ, UK.

Journal of Cell Science
|November 10, 2005
PubMed

Insights

The 12 kDa FK506-binding protein (FKBP12) indirectly modulates calcium (Ca2+) release through IP3 receptors (IP3Rs) in smooth muscle. FKBP12 interacts with mTOR to potentiate and calcineurin to inhibit Ca2+ release via IP3Rs.

Area of Science:

  • Cell Biology
  • Molecular Biology
  • Physiology

Background:

  • Calcium (Ca2+) release from the sarcoplasmic reticulum (SR) via inositol trisphosphate receptors (IP3Rs) is vital for cellular signaling.
  • The 12 kDa FK506-binding protein (FKBP12) is known to associate with IP3Rs and modulate their activity, potentially through interactions with calcineurin.

Purpose of the Study:

  • To investigate the role of FKBP12 in modulating Ca2+ release through IP3Rs in smooth muscle.
  • To determine whether FKBP12 interacts with mammalian target of rapamycin (mTOR) or calcineurin to influence IP3R-mediated Ca2+ release.

Main Methods:

  • Co-immunoprecipitation to assess FKBP12 and IP3R association in colonic and aortic myocytes.
  • Electrophysiological recordings (voltage-clamp) in single myocytes to measure cytosolic Ca2+ concentration ([Ca2+]c) changes upon IP3R activation.
  • Pharmacological inhibition of mTOR (rapamycin, RAD001, LY294002) and calcineurin (FK506, calcineurin inhibitory peptide) to assess their effects on Ca2+ release.

Main Results:

  • FKBP12 co-immunoprecipitated with IP3R in colonic myocytes but not in aortic smooth muscle.
  • In colonic myocytes, rapamycin (mTOR inhibitor) decreased IP3-evoked [Ca2+]c rise, while FK506 (calcineurin inhibitor) potentiated it.
  • In aortic smooth muscle, FK506 and rapamycin did not affect IP3-mediated Ca2+ release, correlating with the lack of FKBP12-IP3R association.

Conclusions:

  • FKBP12 indirectly modulates IP3R-mediated Ca2+ release in smooth muscle through interactions with both mTOR and calcineurin.
  • mTOR potentiates Ca2+ release, while calcineurin inhibits it, with FKBP12 acting as a scaffold or regulator for these interactions.
  • The association of FKBP12 with IP3R is crucial for its modulatory role, as observed in colonic myocytes but not aortic smooth muscle.

Related Concept Videos

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,...
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...
PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

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 rapamycin-insensitive companion...
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...
Nitric Oxide Signaling Pathway01:28

Nitric Oxide Signaling Pathway

Nitric oxide (NO), an inorganic gas, acts as a potent second messenger in most animal and plant tissues. NO diffuses out of the cells that produce it and enters the neighboring cells to generate a downstream response. NO synthase (NOS) catalyzes NO production by the deamination of the amino acid arginine. There are three isoforms of NOS. Endothelial cells have endothelial NOS (eNOS), nerve and muscle cells have neuronal NOS (nNOS), and macrophages produce inducible NOS (iNOS) upon exposure to...
Smooth Muscle Contraction01:25

Smooth Muscle Contraction

Smooth muscle contraction is a complex process vital for various bodily functions, from maintaining blood vessel tension to facilitating the movement of food through the digestive tract. Unlike striated muscles, smooth muscle contraction begins more slowly and lasts longer.
The onset of contraction is triggered by an increase in calcium ions within the sarcoplasm, similar to the process in striated muscle. However, smooth muscles have a relatively smaller reservoir of the sarcoplasmic...