Imaging of insulin signaling in skeletal muscle of living mice shows major role of T-tubules.

Hans P M M Lauritzen; Thorkil Ploug; Clara Prats; Jeremy M Tavaré; Henrik Galbo

Imaging of insulin signaling in skeletal muscle of living mice shows major role of T-tubules.

Hans P M M Lauritzen, Thorkil Ploug, Clara Prats, Jeremy M Tavaré, Henrik Galbo

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

68 Citationer (Scopus)

Abstract

Udgivelsesdato: 2006-May

Originalsprog	Engelsk
Tidsskrift	Diabetes
Vol/bind	55
Udgave nummer	5
Sider (fra-til)	1300-6
Antal sider	6
ISSN	0012-1797
Status	Udgivet - 2006

Bibliografisk note

Keywords: Animals; Biological Transport; Fluorescent Dyes; Glucose Transporter Type 4; Insulin; Kinetics; Mice; Microscopy, Confocal; Microtubules; Muscle, Skeletal; Phosphatidylinositol Phosphates; Receptor, Insulin; Sarcolemma

Citationsformater

@article{6bb19920aca711ddb5e9000ea68e967b,

title = "Imaging of insulin signaling in skeletal muscle of living mice shows major role of T-tubules.",

abstract = "Insulin stimulates glucose transport in skeletal muscle by glucose transporter GLUT4 translocation to sarcolemma and membrane invaginations, the t-tubules. Although muscle glucose uptake plays a key role in insulin resistance and type 2 diabetes, the dynamics of GLUT4 translocation and the signaling involved are not well described. We have now developed a confocal imaging technique to follow trafficking of green fluorescent protein-labeled proteins in living muscle fibers in situ in anesthetized mice. Using this technique, by imaging the dynamics of GLUT4 translocation and phosphatidylinositol 3,4,5 P(3) (PIP(3)) production in response to insulin, here, for the first time, we delineate the temporal and spatial distribution of these processes in a living animal. We find a 10-min delay of maximal GLUT4 recruitment and translocation to t-tubules compared with sarcolemma. Time-lapse imaging of a fluorescent dye after intravenous injection shows that this delay is similar to the time needed for insulin diffusion into the t-tubule system. Correspondingly, immunostaining of muscle fibers shows that insulin receptors are present throughout the t-tubule system. Finally, PIP(3) production, an early event in insulin signaling, progresses slowly along the t-tubules with a 10-min delay between maximal PIP(3) production at sarcolemma compared with deep t-tubules following the appearance of dye-labeled insulin. Our findings in living mice indicate a major role of the t-tubules in insulin signaling in skeletal muscle and show a diffusion-associated delay in insulin action between sarcolemma and inner t-tubules.",

author = "Lauritzen, {Hans P M M} and Thorkil Ploug and Clara Prats and Tavar{\'e}, {Jeremy M} and Henrik Galbo",

note = "Keywords: Animals; Biological Transport; Fluorescent Dyes; Glucose Transporter Type 4; Insulin; Kinetics; Mice; Microscopy, Confocal; Microtubules; Muscle, Skeletal; Phosphatidylinositol Phosphates; Receptor, Insulin; Sarcolemma",

year = "2006",

language = "English",

volume = "55",

pages = "1300--6",

journal = "Diabetes",

issn = "0012-1797",

publisher = "American Diabetes Association",

number = "5",

}

TY - JOUR

T1 - Imaging of insulin signaling in skeletal muscle of living mice shows major role of T-tubules.

AU - Lauritzen, Hans P M M

AU - Ploug, Thorkil

AU - Prats, Clara

AU - Tavaré, Jeremy M

AU - Galbo, Henrik

N1 - Keywords: Animals; Biological Transport; Fluorescent Dyes; Glucose Transporter Type 4; Insulin; Kinetics; Mice; Microscopy, Confocal; Microtubules; Muscle, Skeletal; Phosphatidylinositol Phosphates; Receptor, Insulin; Sarcolemma

PY - 2006

Y1 - 2006

N2 - Insulin stimulates glucose transport in skeletal muscle by glucose transporter GLUT4 translocation to sarcolemma and membrane invaginations, the t-tubules. Although muscle glucose uptake plays a key role in insulin resistance and type 2 diabetes, the dynamics of GLUT4 translocation and the signaling involved are not well described. We have now developed a confocal imaging technique to follow trafficking of green fluorescent protein-labeled proteins in living muscle fibers in situ in anesthetized mice. Using this technique, by imaging the dynamics of GLUT4 translocation and phosphatidylinositol 3,4,5 P(3) (PIP(3)) production in response to insulin, here, for the first time, we delineate the temporal and spatial distribution of these processes in a living animal. We find a 10-min delay of maximal GLUT4 recruitment and translocation to t-tubules compared with sarcolemma. Time-lapse imaging of a fluorescent dye after intravenous injection shows that this delay is similar to the time needed for insulin diffusion into the t-tubule system. Correspondingly, immunostaining of muscle fibers shows that insulin receptors are present throughout the t-tubule system. Finally, PIP(3) production, an early event in insulin signaling, progresses slowly along the t-tubules with a 10-min delay between maximal PIP(3) production at sarcolemma compared with deep t-tubules following the appearance of dye-labeled insulin. Our findings in living mice indicate a major role of the t-tubules in insulin signaling in skeletal muscle and show a diffusion-associated delay in insulin action between sarcolemma and inner t-tubules.

AB - Insulin stimulates glucose transport in skeletal muscle by glucose transporter GLUT4 translocation to sarcolemma and membrane invaginations, the t-tubules. Although muscle glucose uptake plays a key role in insulin resistance and type 2 diabetes, the dynamics of GLUT4 translocation and the signaling involved are not well described. We have now developed a confocal imaging technique to follow trafficking of green fluorescent protein-labeled proteins in living muscle fibers in situ in anesthetized mice. Using this technique, by imaging the dynamics of GLUT4 translocation and phosphatidylinositol 3,4,5 P(3) (PIP(3)) production in response to insulin, here, for the first time, we delineate the temporal and spatial distribution of these processes in a living animal. We find a 10-min delay of maximal GLUT4 recruitment and translocation to t-tubules compared with sarcolemma. Time-lapse imaging of a fluorescent dye after intravenous injection shows that this delay is similar to the time needed for insulin diffusion into the t-tubule system. Correspondingly, immunostaining of muscle fibers shows that insulin receptors are present throughout the t-tubule system. Finally, PIP(3) production, an early event in insulin signaling, progresses slowly along the t-tubules with a 10-min delay between maximal PIP(3) production at sarcolemma compared with deep t-tubules following the appearance of dye-labeled insulin. Our findings in living mice indicate a major role of the t-tubules in insulin signaling in skeletal muscle and show a diffusion-associated delay in insulin action between sarcolemma and inner t-tubules.

M3 - Journal article

C2 - 16644686

SN - 0012-1797

VL - 55

SP - 1300

EP - 1306

JO - Diabetes

JF - Diabetes

IS - 5

ER -