Evidences of Early Senescence in Multiple Myeloma Bone Marrow Mesenchymal Stromal Cells

被引:87
作者
Andre, Thibaud [1 ]
Meuleman, Nathalie [2 ]
Stamatopoulos, Basile [1 ]
De Bruyn, Cecile [2 ]
Pieters, Karlien [1 ]
Bron, Dominique [2 ]
Lagneaux, Laurence [1 ]
机构
[1] Univ Libre Bruxelles, Inst Jules Bordet, Lab Clin Cell Therapy, Brussels, Belgium
[2] Inst Jules Bordet, Dept Hematol, B-1000 Brussels, Belgium
关键词
HEMATOPOIETIC STEM-CELLS; LARGE GENE LISTS; GROWTH-FACTOR; UNDETERMINED SIGNIFICANCE; REPLICATIVE SENESCENCE; MONOCLONAL GAMMOPATHY; SECRETORY PHENOTYPE; TUMOR SUPPRESSION; CANCER; PROLIFERATION;
D O I
10.1371/journal.pone.0059756
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Background: In multiple myeloma, bone marrow mesenchymal stromal cells support myeloma cell growth. Previous studies have suggested that direct and indirect interactions between malignant cells and bone marrow mesenchymal stromal cells result in constitutive abnormalities in the bone marrow mesenchymal stromal cells. Design and Methods: The aims of this study were to investigate the constitutive abnormalities in myeloma bone marrow mesenchymal stromal cells and to evaluate the impact of new treatments. Results: We demonstrated that myeloma bone marrow mesenchymal stromal cells have an increased expression of senescence-associated beta-galactosidase, increased cell size, reduced proliferation capacity and characteristic expression of senescence-associated secretory profile members. We also observed a reduction in osteoblastogenic capacity and immunomodulatory activity and an increase in hematopoietic support capacity. Finally, we determined that current treatments were able to partially reduce some abnormalities in secreted factors, proliferation and osteoblastogenesis. Conclusions: We showed that myeloma bone marrow mesenchymal stromal cells have an early senescent profile with profound alterations in their characteristics. This senescent state most likely participates in disease progression and relapse by altering the tumor microenvironment.
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页数:13
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