4.5 Article

Sex Dimorphic Glucose Transporter-2 Regulation of Hypothalamic Astrocyte Glucose and Energy Sensor Expression and Glycogen Metabolism

Journal

NEUROCHEMICAL RESEARCH
Volume 48, Issue 2, Pages 404-417

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11064-022-03757-z

Keywords

GLUT2; Glycogen phosphorylase; glucokinase; AMPK; Glycogen; Sex differences

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The glucose transporter-2 (GLUT2) in astrocytes plays a sex-specific role in regulating glucose sensor function and glycogen metabolism. GLUT2 stimulates or inhibits glucokinase (GCK) expression in male astrocytes depending on glucose availability, but does not affect female astrocytes. GLUT2 also affects the expression of glycogen synthase (GS) and glycogen phosphorylase (GP) differently in males and females during glucose deprivation. Further research is needed to understand the molecular mechanisms underlying these sex-dimorphic effects.
The plasma membrane glucose transporter-2 (GLUT2) monitors brain cell uptake of the critical nutrient glucose, and functions within astrocytes of as-yet-unknown location to control glucose counter-regulation. Hypothalamic astrocyte-neuron metabolic coupling provides vital cues to the neural glucostatic network. Current research utilized an established hypothalamic primary astrocyte culture model along with gene knockdown tools to investigate whether GLUT2 imposes sex-specific regulation of glucose/energy sensor function and glycogen metabolism in this cell population. Data show that GLUT2 stimulates or inhibits glucokinase (GCK) expression in glucose-supplied versus -deprived male astrocytes, but does not control this protein in female. Astrocyte 5'-AMP-activated protein kinase(alpha 1/2) (AMPK) protein is augmented by GLUT2 in each sex, but phosphoAMPK(alpha 1/2) is coincidently up- (male) or down- (female) regulated. GLUT2 effects on glycogen synthase (GS) diverges in the two sexes, but direction of this control is reversed by glucoprivation in each sex. GLUT2 increases (male) or decreases (female) glycogen phosphorylase-brain type (GPbb) protein during glucoprivation, yet simultaneously inhibits (male) or stimulates (female) GP-muscle type (GPmm) expression. Astrocyte glycogen accumulation is restrained by GLUT2 when glucose is present (male) or absent (both sexes). Outcomes disclose sex-dependent GLUT2 control of the astrocyte glycolytic pathway sensor GCK. Data show that glucose status determines GLUT2 regulation of GS (both sexes), GPbb (female), and GPmm (male), and that GLUT2 imposes opposite control of GS, GPbb, and GPmm profiles between sexes during glucoprivation. Ongoing studies aim to investigate molecular mechanisms underlying sex-dimorphic GLUT2 regulation of hypothalamic astrocyte metabolic-sensory and glycogen metabolic proteins, and to characterize effects of sex-specific astrocyte target protein responses to GLUT2 on glucose regulation.

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