Jezewski_2021_Front.Cell.Infect.Microbiol_11_730413

Reference

Title : Targeting Host Glycolysis as a Strategy for Antimalarial Development - Jezewski_2021_Front.Cell.Infect.Microbiol_11_730413
Author(s) : Jezewski AJ , Lin YH , Reisz JA , Culp-Hill R , Barekatain Y , Yan VC , D'Alessandro A , Muller FL , Odom John AR
Ref : Front Cell Infect Microbiol , 11 :730413 , 2021
Abstract :

Glycolysis controls cellular energy, redox balance, and biosynthesis. Antiglycolytic therapies are under investigation for treatment of obesity, cancer, aging, autoimmunity, and microbial diseases. Interrupting glycolysis is highly valued as a therapeutic strategy, because glycolytic disruption is generally tolerated in mammals. Unfortunately, anemia is a known dose-limiting side effect of these inhibitors and presents a major caveat to development of antiglycolytic therapies. We developed specific inhibitors of enolase - a critical enzyme in glycolysis - and validated their metabolic and cellular effects on human erythrocytes. Enolase inhibition increases erythrocyte susceptibility to oxidative damage and induces rapid and premature erythrocyte senescence, rather than direct hemolysis. We apply our model of red cell toxicity to address questions regarding erythrocyte glycolytic disruption in the context of Plasmodium falciparum malaria pathogenesis. Our study provides a framework for understanding red blood cell homeostasis under normal and disease states and clarifies the importance of erythrocyte reductive capacity in malaria parasite growth.

PubMedSearch : Jezewski_2021_Front.Cell.Infect.Microbiol_11_730413
PubMedID: 34604112

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Citations formats

Jezewski AJ, Lin YH, Reisz JA, Culp-Hill R, Barekatain Y, Yan VC, D'Alessandro A, Muller FL, Odom John AR (2021)
Targeting Host Glycolysis as a Strategy for Antimalarial Development
Front Cell Infect Microbiol 11 :730413

Jezewski AJ, Lin YH, Reisz JA, Culp-Hill R, Barekatain Y, Yan VC, D'Alessandro A, Muller FL, Odom John AR (2021)
Front Cell Infect Microbiol 11 :730413