Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Glucose Absorption Into the Small Intestine01:26

Glucose Absorption Into the Small Intestine

34.3K
Complex carbohydrates consumed cannot be absorbed into the small intestine in their original form. First, they must be hydrolyzed to a monosaccharide form such as glucose or galactose. These monosaccharides are then transported across the intestinal membrane and into the blood via transcellular transport. The intestinal epithelial cells allow the movement of these monosaccharides with a defined 'entry' through membrane transporter proteins present on their apical membrane and...
34.3K
Glucose Transporters01:27

Glucose Transporters

27.0K
Glucose transporters facilitate the transport of glucose across the cell membrane. In addition to glucose, some glucose transporters can also aid the movement of other hexoses such as fructose, mannose, and galactose.
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
27.0K
Membrane Proteins01:30

Membrane Proteins

29.1K
Plasma membranes have integral transmembrane proteins involved in facilitated transport. These proteins are collectively referred to as transport proteins, and they function as either channels for the material or as carriers themselves. Channel proteins have hydrophilic domains exposed to the intracellular and extracellular fluids and a hydrophilic channel through their core that provides a hydrated opening for solutes to pass through the membrane layers. Passage through the channel allows...
29.1K
Secondary Active Transport01:32

Secondary Active Transport

9.1K
One example of how cells use the energy contained in electrochemical gradients is demonstrated by glucose transport into cells. The ion vital to this process is sodium (Na+), which is typically present in higher concentrations extracellularly than in the cytosol. Such a concentration difference is due, in part, to the action of an enzyme "pump" embedded in the cellular membrane that actively expels Na+ from a cell. Importantly, as this pump contributes to the high concentration of...
9.1K
Secondary Active Transport01:55

Secondary Active Transport

136.1K
One example of how cells use the energy contained in electrochemical gradients is demonstrated by glucose transport into cells. The ion vital to this process is sodium (Na+), which is typically present in higher concentrations extracellularly than in the cytosol. Such a concentration difference is due, in part, to the action of an enzyme “pump” embedded in the cellular membrane that actively expels Na+ from a cell. Importantly, as this pump contributes to the high concentration of...
136.1K
Transcellular Transport of Solutes01:23

Transcellular Transport of Solutes

4.5K
Transcellular transport of solutes is the movement of substances like monosaccharides and amino acids through polarized cells. This transport mechanism is primarily seen in epithelial and endothelial cells aided by membrane transport proteins such as channels and transporters. The tight junctions between these cells confine the membrane proteins to the two sides of the cell. The epithelial cells have distinct apical and basolateral domains. In contrast, the endothelial cells show the luminal...
4.5K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Crosstalk between CD8+ T cells and systemic bile acid metabolism shapes antiviral immunity and immunopathology.

JCI insight·2026
Same author

Epigenetic remodeling via HDAC6 inhibition amplifies anti-tumoral immune responses in myeloid leukemia cells.

Cell death & disease·2026
Same author

Sulfated glycosaminoglycans inhibit LCMV entry and modulate antiviral immunity and pathology.

EMBO molecular medicine·2026
Same author

B cells maintain the homeostasis of splenic marginal zone antigen-presenting cells to promote the antiviral CD8<sup>+</sup> T-cell response.

Cellular & molecular immunology·2026
Same author

Type I IFN-dependent FcγRIV signaling in murine monocytes promotes lethal anaphylaxis during viral infections.

The Journal of clinical investigation·2026
Same author

Combined targeted and epigenetic-based therapy enhances antitumor immunity by stabilizing GATA6-dependent MHCI expression in pancreatic ductal adenocarcinoma.

Nature communications·2026

Related Experiment Video

Updated: Dec 18, 2025

A Simple Flow Cytometric Method to Measure Glucose Uptake and Glucose Transporter Expression for Monocyte Subpopulations in Whole Blood
06:28

A Simple Flow Cytometric Method to Measure Glucose Uptake and Glucose Transporter Expression for Monocyte Subpopulations in Whole Blood

Published on: August 12, 2016

17.1K

Glucose transport in lymphocytes.

Florian Lang1,2, Yogesh Singh3, Madhuri S Salker4

  • 1Department of Physiology, Eberhard Karl University, Tubingen, Germany. florian.lang@uni-tuebingen.de.

Pflugers Archiv : European Journal of Physiology
|June 13, 2020
PubMed
Summary

Sodium-glucose cotransporter 1 (SGLT1) is crucial for lymphocyte glucose uptake and function, especially in low-glucose conditions. Its absence impairs host defense against bacterial infections, highlighting its importance in immunity.

Keywords:
Bacterial infectionCancerCytotoxic T lymphocytesEnergy depletionGLUTJanus kinasesJurkat T cellsSGLT1

More Related Videos

An Optimized Protocol to Analyze Glycolysis and Mitochondrial Respiration in Lymphocytes
08:40

An Optimized Protocol to Analyze Glycolysis and Mitochondrial Respiration in Lymphocytes

Published on: November 21, 2016

30.6K
Quantitative Measurement of GLUT4 Translocation to the Plasma Membrane by Flow Cytometry
05:39

Quantitative Measurement of GLUT4 Translocation to the Plasma Membrane by Flow Cytometry

Published on: November 7, 2010

27.0K

Related Experiment Videos

Last Updated: Dec 18, 2025

A Simple Flow Cytometric Method to Measure Glucose Uptake and Glucose Transporter Expression for Monocyte Subpopulations in Whole Blood
06:28

A Simple Flow Cytometric Method to Measure Glucose Uptake and Glucose Transporter Expression for Monocyte Subpopulations in Whole Blood

Published on: August 12, 2016

17.1K
An Optimized Protocol to Analyze Glycolysis and Mitochondrial Respiration in Lymphocytes
08:40

An Optimized Protocol to Analyze Glycolysis and Mitochondrial Respiration in Lymphocytes

Published on: November 21, 2016

30.6K
Quantitative Measurement of GLUT4 Translocation to the Plasma Membrane by Flow Cytometry
05:39

Quantitative Measurement of GLUT4 Translocation to the Plasma Membrane by Flow Cytometry

Published on: November 7, 2010

27.0K

Area of Science:

  • Immunology
  • Cell Biology
  • Metabolism

Background:

  • Lymphocyte glucose uptake occurs via GLUT transporters and the Na+-coupled SGLT1.
  • SGLT1 accumulates glucose against gradients, vital in low-glucose environments.
  • Lymphocytes rely on glycogen-dependent glycolysis in hypoxic conditions like tumors and infections.

Purpose of the Study:

  • To investigate the role of SGLT1 in lymphocyte glucose uptake and function.
  • To determine the impact of SGLT1 deficiency on host defense mechanisms.
  • To clarify the significance of glucose transport for lymphocyte survival and immune response.

Main Methods:

  • Analysis of glucose transport mechanisms in lymphocytes.
  • Investigation of signaling pathways regulating SGLT1.
  • Assessment of host defense in SGLT1 knockout mouse models.

Main Results:

  • SGLT1 facilitates glucose uptake, particularly at low extracellular glucose concentrations.
  • Signaling pathways including PKA, PKC, SGK1, AMPK, JAK2, and JAK3 regulate SGLT1.
  • Genetic knockout of SGLT1 in mice impaired bacterial clearance and led to lethal infections.

Conclusions:

  • SGLT1 plays a critical role in lymphocyte glucose metabolism and function, especially under hypoxic stress.
  • The absence of SGLT1 may compromise lymphocyte survival and immune response.
  • Further research is needed to fully elucidate the role of GLUTs and SGLT1 in lymphocyte-mediated host defense.