Laurenzana Ilaria, Lamorte Daniela, Trino Stefania, De Luca Luciana, Ambrosino Concetta, Zoppoli Pietro, Ruggieri Vitalba, Del Vecchio Luigi, Musto Pellegrino, Caivano Antonella, Falco Geppino
Laboratory of Preclinical and Translational Research, IRCCS-Referral Cancer Center of Basilicata (CROB), Rionero in Vulture, Italy.
Department of Science and Technology, University of Sannio, Benevento, Italy.
Stem Cells Int. 2018 May 27;2018:9863194. doi: 10.1155/2018/9863194. eCollection 2018.
The bone marrow (BM) microenvironment in hematological malignancies (HMs) comprises heterogeneous populations of neoplastic and nonneoplastic cells. Cancer stem cells (CSCs), neoplastic cells, hematopoietic stem cells (HSCs), and mesenchymal stromal/stem cells (MSCs) are all components of this microenvironment. CSCs are the HM initiators and are associated with neoplastic growth and drug resistance, while HSCs are able to reconstitute the entire hematopoietic system; finally, MSCs actively support hematopoiesis. In some HMs, CSCs and neoplastic cells compromise the normal development of HSCs and perturb BM-MSCs. In response, "reprogrammed" MSCs generate a favorable environment to support neoplastic cells. Extracellular vesicles (EVs) are an important cell-to-cell communication type in physiological and pathological conditions. In particular, in HMs, EV secretion participates to unidirectional and bidirectional interactions between neoplastic cells and BM cells. The transfer of EV molecular cargo triggers different responses in target cells; in particular, malignant EVs modify the BM environment in favor of neoplastic cells at the expense of normal HSCs, by interfering with antineoplastic immunity and participating in resistance to treatment. Here, we review the role of EVs in BM cell communication in physiological conditions and in HMs, focusing on the effects of BM niche EVs on HSCs and MSCs.
血液系统恶性肿瘤(HMs)中的骨髓(BM)微环境由肿瘤性和非肿瘤性细胞的异质群体组成。癌症干细胞(CSCs)、肿瘤细胞、造血干细胞(HSCs)和间充质基质/干细胞(MSCs)都是这个微环境的组成部分。CSCs是HMs的起始细胞,与肿瘤生长和耐药性相关,而HSCs能够重建整个造血系统;最后,MSCs积极支持造血作用。在某些HMs中,CSCs和肿瘤细胞损害了HSCs的正常发育并扰乱了BM-MSCs。作为回应,“重新编程”的MSCs产生一个有利的环境来支持肿瘤细胞。细胞外囊泡(EVs)是生理和病理条件下一种重要的细胞间通讯类型。特别是在HMs中,EV分泌参与肿瘤细胞与BM细胞之间的单向和双向相互作用。EV分子货物的转移在靶细胞中引发不同的反应;特别是,恶性EVs通过干扰抗肿瘤免疫和参与治疗抵抗,以牺牲正常HSCs为代价,改变BM环境以利于肿瘤细胞。在这里,我们综述了EVs在生理条件和HMs中BM细胞通讯中的作用,重点关注BM龛EVs对HSCs和MSCs的影响。