Sugar sensing by enterocytes combines polarity, membrane bound detectors and sugar metabolism

Autor: Maude Le Gall, Vanessa Tobin, Edith Brot-Laroche, Emilie Stolarczyk, Armelle Leturque, Véronique Dalet
Přispěvatelé: Centre de Recherche des Cordeliers (CRC (UMR_S 872)), Université Paris Descartes - Paris 5 (UPD5)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), ALFEDIAM Merck Lipha, Institut Benjamin Delessert, AIP ATC Nutrition, Grant Number: ASEO22129DSA., Université Pierre et Marie Curie - Paris 6 (UPMC)-Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Centre de Recherche des Cordeliers ( CRC (UMR_S 872) ), Université Pierre et Marie Curie - Paris 6 ( UPMC ) -Université Paris Descartes - Paris 5 ( UPD5 ) -Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Centre National de la Recherche Scientifique ( CNRS ), Le Gall, Maude
Rok vydání: 2007
Předmět:
Sucrose
MESH : RNA
Messenger

[SDV.MHEP.PHY] Life Sciences [q-bio]/Human health and pathology/Tissues and Organs [q-bio.TO]
MESH : Promoter Regions
Genetic

MESH : Green Fluorescent Proteins
MESH: Protein Structure
Tertiary

MESH: Enterocytes
Mice
0302 clinical medicine
Gene expression
sugar metabolism
MESH : Glucose Transporter Type 5
MESH: Animals
MESH : Glucose Transporter Type 2
MESH : Sucrase
MESH: Oligo-1
6-Glucosidase

0303 health sciences
MESH: Sweetening Agents
MESH : Enterocytes
Jejunum
MESH : Protein Structure
Tertiary

endocrine system
MESH : Cloning
Molecular

Monosaccharide Transport Proteins
MESH : Sodium-Glucose Transporter 1
Oligo-1
6-Glucosidase

Transfection
03 medical and health sciences
MESH: Green Fluorescent Proteins
Sodium-Glucose Transporter 1
MESH: Promoter Regions
Genetic

Humans
MESH: Cloning
Molecular

RNA
Messenger

[ SDV.BBM ] Life Sciences [q-bio]/Biochemistry
Molecular Biology

MESH: Humans
MESH : Glucose
[ SDV.BC ] Life Sciences [q-bio]/Cellular Biology
MESH : Humans
MESH: Sucrose
MESH : Caco-2 Cells
Fructose
Protein Structure
Tertiary

Mice
Inbred C57BL

Enterocytes
Glucose
chemistry
MESH: Jejunum
Sweetening Agents
GLUT2
MESH: Glucose Transporter Type 2
MESH: Glucose Transporter Type 5
GLUT5
MESH: Fructose
030217 neurology & neurosurgery
Physiology
[ SDV.AEN ] Life Sciences [q-bio]/Food and Nutrition
Clinical Biochemistry
enterocyte
MESH: Mice
Knockout

MESH : Fructose
chemistry.chemical_compound
glucose signalling
MESH: Hexoses
MESH : Jejunum
Cloning
Molecular

Receptor
Promoter Regions
Genetic

MESH : Oligo-1
6-Glucosidase

Glucose Transporter Type 2
Mice
Knockout

biology
[ SDV.MHEP.PHY ] Life Sciences [q-bio]/Human health and pathology/Tissues and Organs [q-bio.TO]
Glucose Transporter Type 5
Cell Polarity
MESH: Glucose
Biochemistry
MESH: Monosaccharide Transport Proteins
MESH: Sodium-Glucose Transporter 1
MESH: Caco-2 Cells
MESH : Transfection
MESH: Cell Polarity
MESH : Cell Polarity
Sucrase
Green Fluorescent Proteins
MESH : Mice
Inbred C57BL

[SDV.BC]Life Sciences [q-bio]/Cellular Biology
MESH: Mice
Inbred C57BL

MESH : Mice
[SDV.BBM] Life Sciences [q-bio]/Biochemistry
Molecular Biology

[SDV.MHEP.PHY]Life Sciences [q-bio]/Human health and pathology/Tissues and Organs [q-bio.TO]
Animals
[SDV.BBM]Life Sciences [q-bio]/Biochemistry
Molecular Biology

sweet taste receptor
Sugar
[SDV.BC] Life Sciences [q-bio]/Cellular Biology
MESH: Mice
030304 developmental biology
MESH : Monosaccharide Transport Proteins
MESH: RNA
Messenger

Hexoses
MESH: Transfection
Cell Biology
Metabolism
Gustducin
MESH : Sucrose
[SDV.AEN] Life Sciences [q-bio]/Food and Nutrition
MESH : Sweetening Agents
MESH: Sucrase
biology.protein
MESH : Mice
Knockout

MESH : Animals
Caco-2 Cells
MESH : Hexoses
[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition
Zdroj: Journal of Cellular Physiology
Journal of Cellular Physiology, Wiley, 2007, 213 (3), pp.834-43. ⟨10.1002/jcp.21245⟩
Journal of Cellular Physiology, 2007, 213 (3), pp.834-43. ⟨10.1002/jcp.21245⟩
Journal of Cellular Physiology, Wiley, 2007, 213 (3), pp.834-43. 〈10.1002/jcp.21245〉
ISSN: 1097-4652
0021-9541
DOI: 10.1002/jcp.21245⟩
Popis: Sugar consumption and subsequent sugar metabolism are known to regulate the expression of genes involved in intestinal sugar absorption and delivery. Here we investigate the hypothesis that sugar-sensing detectors in membranes facing the intestinal lumen or the bloodstream can also modulate intestinal sugar absorption. We used wild-type and GLUT2-null mice, to show that dietary sugars stimulate the expression of sucrase-isomaltase (SI) and L-pyruvate kinase (L-PK) by GLUT2-dependent mechanisms, whereas the expression of GLUT5 and SGLT1, did not rely on the presence of GLUT2. By providing sugar metabolites, sugar transporters, including GLUT2, fuelled a sensing pathway. In Caco2/TC7 enterocytes, we could disconnect the sensing triggered by detector from that produced by metabolism, and found that GLUT2 generated a metabolism-independent pathway to stimulate the expression of SI and L-PK. In cultured enterocytes, both apical and basolateral fructose could increase the expression of GLUT5, conversely, basolateral sugar administration could stimulate the expression of GLUT2. Finally, we located the sweet-taste receptors T1R3 and T1R2 in plasma membranes, and we measured their cognate Galpha Gustducin mRNA levels. Furthermore, we showed that a T1R3 inhibitor altered the fructose-induced expression of SGLT1, GLUT5, and L-PK. Intestinal gene expression is thus controlled by a combination of at least three sugar-signaling pathways triggered by sugar metabolites and membrane sugar receptors that, according to membrane location, determine sugar-sensing polarity. This provides a rationale for how intestine adapts sugar delivery to blood and dietary sugar provision. J. Cell. Physiol. 213:834–843. © 2007 Wiley-Liss, Inc.
Databáze: OpenAIRE