Erk5 in Bone Marrow Mesenchymal Stem Cells Regulates Bone Homeostasis by Preventing Osteogenesis in Adulthood

被引:16
作者
Horie, Tetsuhiro [1 ]
Fukasawa, Kazuya [1 ]
Yamada, Takanori [1 ]
Mizuno, Seiya [2 ]
Iezaki, Takashi [1 ]
Tokumura, Kazuya [1 ]
Iwahashi, Sayuki [1 ]
Sakai, Shiho [1 ]
Suzuki, Akane [1 ]
Kubo, Takuya [1 ]
Osumi, Ryoma [1 ]
Tomizawa, Akane [1 ]
Ochi, Hiroki [3 ]
Sato, Shingo [4 ]
Kaneda, Katsuyuki [5 ]
Takahashi, Satoru [2 ]
Hinoi, Eiichi [1 ,6 ]
机构
[1] Gifu Pharmaceut Univ, Dept Bioact Mol, Pharmacol, Gifu 5011196, Japan
[2] Univ Tsukuba, Lab Anim Resource Ctr, 1-1-1 Tennodai, Tsukuba, Ibaraki, Japan
[3] Natl Rehabil Ctr Persons Disabil, Res Inst, Dept Rehabil Motor Funct, Tokorozawa, Saitama, Japan
[4] Tokyo Med & Dent Univ, Ctr Innovat Canc Treatment, Tokyo, Japan
[5] Kanazawa Univ, Div Pharmaceut Sci, Lab Mol Pharmacol, Grad Sch, Kanazawa, Ishikawa, Japan
[6] Gifu Univ, United Grad Sch Drug Discovery & Med Informat Sci, Gifu, Japan
基金
日本学术振兴会;
关键词
bone marrow mesenchymal stem cells; extracellular signal-regulated kinase 5; Smad specific E3 ubiquitin protein ligase 2; bone homeostasis; osteogenesis; CRE RECOMBINASE; STROMAL CELLS; LEPTIN; EXPRESSION; MICE; DRIVEN; NICHE;
D O I
10.1093/stmcls/sxac011
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Extracellular signal-regulated kinase 5 (Erk5) belongs to the mitogen-activated protein kinase (MAPK) family. Previously, we demonstrated that Erk5 directly phosphorylates Smad-specific E3 ubiquitin protein ligase 2 (Smurf2) at Thr(249) (Smurf2(Thr249)) to activate its E3 ubiquitin ligase activity. Although we have clarified the importance of Erk5 in embryonic mesenchymal stem cells (MSCs) on skeletogenesis, its role in adult bone marrow (BM)-MSCs on bone homeostasis remains unknown. Leptin receptor-positive (LepR(+)) BM-MSCs represent a major source of bone in adult bone marrow and are critical regulators of postnatal bone homeostasis. Here, we identified Erk5 in BM-MSCs as an important regulator of bone homeostasis in adulthood. Bone marrow tissue was progressively osteosclerotic in mice lacking Erk5 in LepR(+) BM-MSCs with age, accompanied by increased bone formation and normal bone resorption in vivo. Erk5 deficiency increased the osteogenic differentiation of BM-MSCs along with a higher expression of Runx2 and Osterix, essential transcription factors for osteogenic differentiation, without affecting their stemness in vitro. Erk5 deficiency decreased Smurf2(Thr249) phosphorylation and subsequently increased Smad1/5/8-dependent signaling in BM-MSCs. The genetic introduction of the Smurf2(T249E) mutant (a phosphomimetic mutant) suppressed the osteosclerotic phenotype in Erk5-deficient mice. These findings suggest that the Erk5-Smurf2(Thr249) axis in BM-MSCs plays a critical role in the maintenance of proper bone homeostasis by preventing excessive osteogenesis in adult bone marrow.
引用
收藏
页码:411 / 422
页数:12
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