Key Laboratory of Functional Protein Research of Guangdong Higher Education Institutes, Department of Biology, Jinan University, Guangzhou 510632, China.
Research Center for Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou 510006, China.
Cell Rep. 2019 Feb 19;26(8):2166-2177.e9. doi: 10.1016/j.celrep.2019.01.082.
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 from the plasma membrane and presents it to PLCβ3, enabling IP generation and subsequent Ca-dependent bioenergetics. LYZ-81 binds ORP4L competitively with PIP and blocks PIP hydrolysis, resulting in defective Ca 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.
白血病干细胞(LSCs)是异常造血干细胞(HSCs)的一个稀有亚群,它能促进白血病的发生,并导致治疗后高复发率。深入了解 LSCs 的存活机制将有助于确定治疗方法的靶点。在这里,我们开发了一种抑制剂 LYZ-81,它能以高亲和力和特异性靶向 ORP4L,选择性地在体外和体内清除 LSCs。ORP4L 在 LSCs 中表达,但不在正常 HSCs 中表达,对 LSC 的能量代谢和存活至关重要。它从质膜中提取 PIP 并将其呈现给 PLCβ3,从而产生 IP 并随后进行 Ca 依赖性能量代谢。LYZ-81 通过与 PIP 竞争结合 ORP4L 并阻断 PIP 水解,导致 Ca 信号转导缺陷。研究结果表明,通过抑制 ORP4L 可以清除 LSCs,LYZ-81 可能成为开发消除 LSCs 的药物的起点,从而最终治愈白血病。