Pyrroline-5-Carboxylate Reductase 1 Directs the Cartilage Protective and Regenerative Potential of Murphy Roths Large Mouse Mesenchymal Stem Cells

被引:4
|
作者
Tejedor, Gautier [1 ]
Contreras-Lopez, Rafael [1 ]
Barthelaix, Audrey [1 ]
Ruiz, Maxime [1 ]
Noel, Daniele [1 ,2 ]
De Ceuninck, Frederic [3 ]
Pastoureau, Philippe [3 ]
Luz-Crawford, Patricia [4 ]
Jorgensen, Christian [1 ,2 ]
Djouad, Farida [1 ]
机构
[1] Univ Montpellier, INSERM, IRMB, Montpellier, France
[2] CHU Montpellier, Montpellier, France
[3] Inst Rech Servier, Ctr Therapeut Innovat, Immunoinflammatory Dis, Croissy Sur Seine, France
[4] Univ Andes, Fac Med, Lab Inmunol Celular & Mol, Santiago, Chile
关键词
MRL mouse; regeneration; mesenchymal stem cells; PYCR1; metabolism; chondrogenesis; chondrocyte; chondroprotection; PROLINE METABOLISM; STROMAL CELLS; OXYGEN-TENSION; IN-VITRO; PROLIFERATION; CHONDROCYTES; DIFFERENTIATION; OSTEOARTHRITIS; INFLAMMATION; GLYCOLYSIS;
D O I
10.3389/fcell.2021.604756
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Murphy Roths Large (MRL) mice possess outstanding capacity to regenerate several tissues. In the present study, we investigated whether this regenerative potential could be associated with the intrinsic particularities possessed by their mesenchymal stem cells (MSCs). We demonstrated that MSCs derived from MRL mice (MRL MSCs) display a superior chondrogenic potential than do C57BL/6 MSC (BL6 MSCs). This higher chondrogenic potential of MRL MSCs was associated with a higher expression level of pyrroline-5-carboxylate reductase 1 (PYCR1), an enzyme that catalyzes the biosynthesis of proline, in MRL MSCs compared with BL6 MSCs. The knockdown of PYCR1 in MRL MSCs, using a specific small interfering RNA (siRNA), abolishes their chondrogenic potential. Moreover, we showed that PYCR1 silencing in MRL MSCs induced a metabolic switch from glycolysis to oxidative phosphorylation. In two in vitro chondrocyte models that reproduce the main features of osteoarthritis (OA) chondrocytes including a downregulation of chondrocyte markers, a significant decrease of PYCR1 was observed. A downregulation of chondrocyte markers was also observed by silencing PYCR1 in freshly isolated healthy chondrocytes. Regarding MSC chondroprotective properties on chondrocytes with OA features, we showed that MSCs silenced for PYCR1 failed to protect chondrocytes from a reduced expression of anabolic markers, while MSCs overexpressing PYCR1 exhibited an increased chondroprotective potential. Finally, using the ear punch model, we demonstrated that MRL MSCs induced a regenerative response in non-regenerating BL6 mice, while BL6 and MRL MSCs deficient for PYCR1 did not. In conclusion, our results provide evidence that MRL mouse regenerative potential is, in part, attributed to its MSCs that exhibit higher PYCR1-dependent glycolytic potential, differentiation capacities, chondroprotective abilities, and regenerative potential than BL6 MSCs.
引用
收藏
页数:13
相关论文
共 3 条
  • [1] Shikonin induces apoptosis and autophagy via downregulation of pyrroline-5-carboxylate reductase1 in hepatocellular carcinoma cells
    Zhang, Junli
    Shang, Ling
    Jiang, Wendi
    Wu, Wenjuan
    BIOENGINEERED, 2022, 13 (03) : 7904 - 7918
  • [2] Pyrroline-5-Carboxylate Reductase 1: a novel target for sensitizing multiple myeloma cells to bortezomib by inhibition of PRAS40-mediated protein synthesis
    Inge Oudaert
    Hatice Satilmis
    Philip Vlummens
    Wouter De Brouwer
    Anke Maes
    Dirk Hose
    Elke De Bruyne
    Bart Ghesquière
    Karin Vanderkerken
    Kim De Veirman
    Eline Menu
    Journal of Experimental & Clinical Cancer Research, 41
  • [3] Pyrroline-5-Carboxylate Reductase 1: a novel target for sensitizing multiple myeloma cells to bortezomib by inhibition of PRAS40-mediated protein synthesis
    Oudaert, Inge
    Satilmis, Hatice
    Vlummens, Philip
    De Brouwer, Wouter
    Maes, Anke
    Hose, Dirk
    De Bruyne, Elke
    Ghesquiere, Bart
    Vanderkerken, Karin
    De Veirman, Kim
    Menu, Eline
    JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2022, 41 (01)