Glut-1

Author: Prof. Dr. med. Peter Altmeyer

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Last updated on: 21.08.2021

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Synonym(s)

erythrocyte/brain hexose facilitator; Glucose transporter protein

Definition
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GLUT-1 is a protein of the cell membranes of erythrocytes and cells of the blood-brain barrier. Functionally, it is a transport protein (glucose transporter), a glycoprotein with a molecular mass of 55,000, which enables the introduction of glucose (and other sugars) and vitamin C into the cell interior via a channel. GLUT-1 regulates the glucose uptake in erythrocytes and the brain substance. The coding gene on chromosome 1 is called SLC2A1 gene (solute carrier family 2, facilitated glucose transporter member 1). Mutations in the SLC2A1 gene can cause the GLUT1 deficit syndrome.

General information
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Patients with type 2 diabetes mellitus show decreased expression of GLUT1 and decreased glucose uptake in skeletal muscle cells. In the mesangium cell of the renal glomerula there is an increased expression of GLUT1. This leads to increased glucose uptake and excessive production of extracellular matrix in the kidney. Increased pressure in the capillaries of the renal glomerula or an increase in angiotensin II also promotes the expression of GLUT1. This mechanism is thought to be a cause of renal damage caused by hypertension or obesity(nephrosclerosis). GLUT-1 is a specific marker for all developmental stages of infantile hematoma, is further expressed in other benign vascular tumors (e.g. hemangioma, tufted) but also in malignancies such as malignant melanoma, squamous cell carcinoma of the oral mucosa and various adenocarcinomas. Adenocarcinomas.

A congenital defect of the SLC2A1 gene can lead to GLUT1 deficiency (GLUT1 deficit syndrome).

Literature
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  6. Mihic-Probst D et al (2012) Tumor cell plasticity and angiogenesis in human melanomas. PLoS One 7:e33571 .

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Last updated on: 21.08.2021