CXCL13 chemokine is a novel player in multiple myeloma osteolytic microenvironment, M2 macrophage polarization, and tumor progression

被引:23
|
作者
Beider, Katia [1 ,2 ]
Voevoda-Dimenshtein, Valeria [1 ,2 ]
Zoabi, Ali [1 ,2 ]
Rosenberg, Evgenia [1 ,2 ]
Magen, Hila [1 ,2 ]
Ostrovsky, Olga [1 ,2 ]
Shimoni, Avichai [1 ,2 ]
Weiss, Lola [3 ]
Abraham, Michal [3 ]
Peled, Amnon [3 ]
Nagler, Arnon [1 ,2 ]
机构
[1] Tel Aviv Univ, Chaim Sheba Med Ctr, Div Hematol, Tel Hashomer, Israel
[2] Tel Aviv Univ, Chaim Sheba Med Ctr, CBB, Tel Hashomer, Israel
[3] Hebrew Univ Hosp, Goldyne Savad Inst Gene Therapy, Jerusalem, Israel
关键词
RANK LIGAND EXPRESSION; BONE-MARROW; CELL LYMPHOMA; PROSTATE-CANCER; STROMAL CELLS; RECEPTOR; CXCR5; CARCINOMA; IBRUTINIB; DISEASE;
D O I
10.1186/s13045-022-01366-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background We assessed the mechanism by which multiple myeloma (MM) shapes the bone marrow (BM) microenvironment and affects M phi polarization. Methods In vivo xenograft model of BM-disseminated human myeloma, as well as analysis of MM cell lines, stromal components, and primary samples from patients with MM, was utilized. Results Analysis of the BM from MM-bearing mice inoculated with human CXCR4-expressing RPMI8226 cells revealed a significant increase in M2 M phi cell numbers (p < 0.01). CXCL13 was one of the most profoundly increased factors upon MM growth with increased levels in the blood of MM-bearing animals. Myeloid cells were the main source of the increased murine CXCL13 detected in MM-infiltrated BM. MM cell lines induced CXCL13 and concurrent expression of M2 markers (MERTK, CD206, CD163) in co-cultured human M phi in vitro. Interaction with M phi reciprocally induced CXCL13 expression in MM cell lines. Mechanistically, TGF beta signaling was involved in CXCL13 induction in MM cells, while BTK signaling was implicated in MM-stimulated increase of CXCL13 in M phi. Recombinant CXCL13 increased RANKL expression and induced TRAP+ osteoclast (OC) formation in vitro, while CXCL13 neutralization blocked these activities. Moreover, mice inoculated with CXCL13-silenced MM cells developed significantly lower BM disease. Reduced tumor load correlated with decreased numbers of M2 M phi in BM, decreased bone disease, and lower expression of OC-associated genes. Finally, higher levels of CXCL13 were detected in the blood and BM samples of MM patients in comparison with healthy individuals. Conclusions Altogether, our findings suggest that bidirectional interactions of M phi with MM tumor cells result in M2 M phi polarization, CXCL13 induction, and subsequent OC activation, enhancing their ability to support bone resorption and MM progression. CXCL13 may thus serve as a potential novel target in MM.
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页数:19
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