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2134 Metabolomic Profiling Identifies Hypoxia-Induced Imbalanced Lands' Cycle Promotes Sickling and Disease Progression

Red Cells and Erythropoiesis, Structure and Function, Metabolism, and Survival, Excluding Iron
Program: Oral and Poster Abstracts
Session: 101. Red Cells and Erythropoiesis, Structure and Function, Metabolism, and Survival, Excluding Iron: Poster II
Sunday, December 6, 2015, 6:00 PM-8:00 PM
Hall A, Level 2 (Orange County Convention Center)

Hongyu Wu, PhD1*, Mikhail Bogdanov, PhD2*, Yujin Zhang, MD3*, Kaiqi Sun, BS3,4, Anren Song, PhD2*, Hong Liu, MD3*, Morayo G, Adebiyi2*, Danny C. Alexander5*, Michael V. Milburn5*, Modupe Idowu, MD6, Harinder S. Juneja, MD6 and Yang Xia, MD, Ph.D4,7

1Univeristy of Texas-Medical School, Houston, TX
2University of Texas-Medical School, Houston, TX
3Department of Biochemistry and Molecular Biology, UTHSC-Houston Medical School, Houston, TX
4University of Texas Graduate School of Biomedical Science, Houston, TX
53Metabolon, Inc.,, Durham, NC
6Department of Internal Medicine-Hematology Division, University of Texas Health Science Center at Houston, Houston, TX
7Department of Biochemistry and Molecular Biology, University of Texas Medical School at Houston, Houston, TX

Sickle cell disease (SCD) is a prevalent hemolytic genetic disorder with high morbidity and mortality affecting millions of individuals worldwide. Although it is well accepted that deoxygenation and polymerization of sickle hemoglobin (HbS) are initial triggers for sickling, it has been known for more than three decades that abnormal membrane lipid organization and composition are found in sickle erythrocyte. Early studies showed some lipids are altered in sickle erythrocytes, however, no studies have identified overall membrane lipid alteration and functional role of those altered specific lipids in SCD. Using unbiased metabolomic profiling, we found that lysophospholipids (LPLs), particularly lysophosphocholines (LysoPCs), were significantly elevated inside erythrocytes of mice with SCD due to imbalanced Lands’ cycle. Lands’ cycle containing two concerted enzymes: phospholipases A2 (PLA2s) and lysophospholipid acyltransferases (LPLATs) was initially discovered in 1958. However, its function and cellular regulation in membrane homeostasis in SCD remain unrecognized prior to our metabolomics screening. Here, we demonstrated that enhancing imbalanced Lands’ cycle promotes a process of sickling and disease progression in mice by inducing LysoPC content inside erythrocytes. Significantly, correcting impaired Lands’ cycle reduced LysoPC levels within erythrocytes and attenuated sickling and disease progression in mice. Mechanistically, we revealed that hypoxia-mediated MEK/ERK activation underlies imbalanced Lands’ cycle by preferentially inducing activity of PLA2 but not LPCAT1 in mouse sickle erythrocytes. Additionally, the detrimental role of impaired Lands’ cycle-induced LysoPC production in sickling via MEK/ERK-dependent activation of PLA2 in SCD patients mirrors our mouse finding. Overall, our studies have identified a pathological role of imbalanced Lands’ cycle in SCD, revealed molecular basis regulating Lands’ cycle and immediately provided novel therapeutic possibilities for the disease.

Disclosures: No relevant conflicts of interest to declare.

*signifies non-member of ASH