Institute for Tumor Biology and Experimental Therapy, Georg-Speyer-Haus, Frankfurt am Main, Germany.
Institute of Biochemistry II, Medical Faculty, Goethe University, Frankfurt am Main, Germany.
Blood Adv. 2023 Apr 11;7(7):1190-1203. doi: 10.1182/bloodadvances.2022007528.
Leukemia cells reciprocally interact with their surrounding bone marrow microenvironment (BMM), rendering it hospitable to leukemia cell survival, for instance through the release of small extracellular vesicles (sEVs). In contrast, we show here that BMM deficiency of pleckstrin homology domain family M member 1 (PLEKHM1), which serves as a hub between fusion and secretion of intracellular vesicles and is important for vesicular secretion in osteoclasts, accelerates murine BCR-ABL1+ B-cell acute lymphoblastic leukemia (B-ALL) via regulation of the cargo of sEVs released by BMM-derived mesenchymal stromal cells (MSCs). PLEKHM1-deficient MSCs and their sEVs carry increased amounts of syntenin and syndecan-1, resulting in a more immature B-cell phenotype and an increased number/function of leukemia-initiating cells (LICs) via focal adhesion kinase and AKT signaling in B-ALL cells. Ex vivo pretreatment of LICs with sEVs derived from PLEKHM1-deficient MSCs led to a strong trend toward acceleration of murine and human BCR-ABL1+ B-ALL. In turn, inflammatory mediators such as recombinant or B-ALL cell-derived tumor necrosis factor α or interleukin-1β condition murine and human MSCs in vitro, decreasing PLEKHM1, while increasing syntenin and syndecan-1 in MSCs, thereby perpetuating the sEV-associated circuit. Consistently, human trephine biopsies of patients with B-ALL showed a reduced percentage of PLEKHM1+ MSCs. In summary, our data reveal an important role of BMM-derived sEVs for driving specifically BCR-ABL1+ B-ALL, possibly contributing to its worse prognosis compared with BCR-ABL1- B-ALL, and suggest that secretion of inflammatory cytokines by cancer cells in general may similarly modulate the tumor microenvironment.
白血病细胞与其周围的骨髓微环境(BMM)相互作用,使白血病细胞能够在其中生存,例如通过释放小细胞外囊泡(sEVs)。相比之下,我们在这里展示的是,BMM 中pleckstrin homology domain family M member 1(PLEKHM1)的缺乏会加速小鼠 BCR-ABL1+B 细胞急性淋巴细胞白血病(B-ALL),PLEKHM1 作为细胞内囊泡融合和分泌的枢纽,对于破骨细胞中囊泡的分泌很重要。BCR-ABL1+B 细胞急性淋巴细胞白血病来源于骨髓间充质干细胞(MSCs)的 BMM 缺陷,并调节由 BMM 衍生的间充质基质细胞(MSCs)释放的 sEV 的货物。PLEKHM1 缺陷型 MSC 及其 sEV 携带更多的 syntenin 和 syndecan-1,导致通过粘着斑激酶和 AKT 信号通路在 B-ALL 细胞中出现更不成熟的 B 细胞表型和更多数量/功能的白血病起始细胞(LICs)。体外预处理 LICs 用来源于 PLEKHM1 缺陷型 MSC 的 sEV 导致小鼠和人 BCR-ABL1+B-ALL 加速的强烈趋势。反过来,炎性介质如重组或 B-ALL 细胞衍生的肿瘤坏死因子α或白细胞介素-1β在体外调节小鼠和人 MSC,降低 PLEKHM1,同时增加 MSC 中的 syntenin 和 syndecan-1,从而使 sEV 相关的循环得以持续。一致地,患有 B-ALL 的患者的人活检标本显示 PLEKHM1+MSC 的百分比降低。总之,我们的数据揭示了 BMM 来源的 sEV 对驱动特异性 BCR-ABL1+B-ALL 的重要作用,可能导致其与 BCR-ABL1-B-ALL 相比预后更差,并表明癌细胞分泌的炎性细胞因子可能同样调节肿瘤微环境。