Effect of PKM2 on Osteogenic and Adipogenic Differentiation of Bone Marrow Mesenchymal Stem Cells in Myeloma Bone Disease.
10.19746/j.cnki.issn.1009-2137.2023.01.027
- Author:
Jiang-Hua DING
1
;
Shao-Lin YANG
2
;
Shu-Lang ZHU
3
Author Information
1. Department of Hematology & Oncology, Jiujiang University Clinical Medical College & Affiliated Hospital, Jiujiang 332000, Jiangxi Province, China.
2. Department of Pharmacy, Jiujiang University Clinical Medical College & Affiliated Hospital, Jiujiang 332000, Jiangxi Province, China.
3. Department of Osteology, Jiujiang University Clinical Medical College & Affiliated Hospital, Jiujiang 332000, Jiangxi Province, China.E-mail: 104308204@qq.com.
- Publication Type:Journal Article
- Keywords:
adipogenesis;
bone marrow mesenchymal stem cell;
myeloma bone disease;
osteogenesis;
pyruvate kinase M2
- MeSH:
Humans;
Adipogenesis;
Bone Diseases/metabolism*;
Bone Marrow Cells;
Cell Differentiation;
Cells, Cultured;
Mesenchymal Stem Cells/physiology*;
Multiple Myeloma/metabolism*;
Orlistat/pharmacology*;
Osteogenesis/genetics*
- From:
Journal of Experimental Hematology
2023;31(1):170-178
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate the expression of pyruvate kinase M2 (PKM2) in bone marrow mesenchymal stem cells (BMSCs) in myeloma bone disease (MBD) and its effect on osteogenic and adipogenic differentiation of BMSCs.
METHODS:BMSCs were isolated from bone marrow of five patients with multiple myeloma (MM) (MM group) and five with iron deficiency anemia (control group) for culture and identification. The expression of PKM2 protein were compared between the two groups. The differences between osteogenic and adipogenic differentiation of BMSCs were assessed by using alkaline phosphatase (ALP) and oil red O staining, and detecting marker genes of osteogenesis and adipogenesis. The effect of MM cell line (RPMI-8226) and BMSCs co-culture on the expression of PKM2 was explored. Functional analysis was performed to investigate the correlations of PKM2 expression of MM-derived BMSCs with osteogenic and adipogenic differentiation by employing PKM2 activator and inhibitor. The role of orlistat was explored in regulating PKM2 expression, osteogenic and adipogenic differentiation of MM-derived BMSCs.
RESULTS:Compared with control, MM-originated BMSCs possessed the ability of increased adipogenic and decreased osteogenic differentiation, and higher level of PKM2 protein. Co-culture of MM cells with BMSCs markedly up-regulated the expression of PKM2 of BMSCs. Up-regulation of PKM2 expression could promote adipogenic differentiation and inhibit osteogenic differentiation of MM-derived BMSCs, while down-regulation of PKM2 showed opposite effect. Orlistat significantly promoted osteogenic differentiation in MM-derived BMSCs via inhibiting the expression of PKM2.
CONCLUSION:The overexpression of PKM2 can induce the inhibition of osteogenic differentiation of BMSCs in MBD. Orlistat can promote the osteogenic differentiation of BMSCs via inhibiting the expression of PKM2, indicating a potential novel agent of anti-MBD therapy.
