ORP4L Extracts and Presents PIP2 from Plasma Membrane for PLCβ3 Catalysis: Targeting It Eradicates Leukemia Stem Cells
Author(s) -
Wenbin Zhong,
MengYang Xu,
Chanjuan Li,
Biying Zhu,
Xiuye Cao,
Dan Li,
Huanzhao Chen,
Chunxiu Hu,
Rong Li,
Chengwei Luo,
Guoping Pan,
Wenqiang Zhang,
Chaofeng Lai,
Tong Wang,
Xin Du,
Hong Chen,
Guowang Xu,
Vesa M. Olkkonen,
Pingsheng Lei,
Jun Xu,
Daoguang Yan
Publication year - 2019
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2019.01.082
Subject(s) - haematopoiesis , leukemia , stem cell , in vivo , bioenergetics , biology , in vitro , membrane , biochemistry , microbiology and biotechnology , cancer research , chemistry , immunology , mitochondrion , genetics
Leukemia stem cells (LSCs) are a rare subpopulation of abnormal hematopoietic stem cells (HSCs) that propagates leukemia and are responsible for the high frequency of relapse in therapies. Detailed insights into LSCs' survival will facilitate the identification of targets for therapeutic approaches. Here, we develop an inhibitor, LYZ-81, which targets ORP4L with high affinity and specificity and selectively eradicates LCSs in vitro and in vivo. ORP4L is expressed in LSCs but not in normal HSCs and is essential for LSC bioenergetics and survival. It extracts PIP 2 from the plasma membrane and presents it to PLCβ3, enabling IP 3 generation and subsequent Ca 2+ -dependent bioenergetics. LYZ-81 binds ORP4L competitively with PIP 2 and blocks PIP 2 hydrolysis, resulting in defective Ca 2+ signaling. The results provide evidence that LSCs can be eradicated through the inhibition of ORP4L by LYZ-81, which may serve as a starting point of drug development for the elimination of LSCs to eventually cure leukemia.
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