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本文引用的文献

1
Medical therapies with adult stem/progenitor cells (MSCs): a backward journey from dramatic results in vivo to the cellular and molecular explanations.成体/祖细胞(MSCs)的医学治疗方法:从体内戏剧性的结果到细胞和分子解释的倒退之旅。
J Cell Biochem. 2012 May;113(5):1460-9. doi: 10.1002/jcb.24046.
2
Amelioration of a mouse model of osteogenesis imperfecta with hematopoietic stem cell transplantation: microcomputed tomography studies.用造血干细胞移植改善成骨不全症小鼠模型:微计算机断层扫描研究。
Exp Hematol. 2010 Jul;38(7):593-602. doi: 10.1016/j.exphem.2010.04.008. Epub 2010 Apr 24.
3
Mesenchymal stem cells as therapeutics.间充质干细胞治疗。
Annu Rev Biomed Eng. 2010 Aug 15;12:87-117. doi: 10.1146/annurev-bioeng-070909-105309.
4
Hematopoietic stem cell origin of connective tissues.结缔组织的造血干细胞起源。
Exp Hematol. 2010 Jul;38(7):540-7. doi: 10.1016/j.exphem.2010.04.005. Epub 2010 Apr 20.
5
The association of human mesenchymal stem cells with BMP-7 improves bone regeneration of critical-size segmental bone defects in athymic rats.人骨髓间充质干细胞与 BMP-7 的联合应用可改善免疫缺陷大鼠临界尺寸节段性骨缺损的骨再生。
Bone. 2010 Jul;47(1):117-26. doi: 10.1016/j.bone.2010.03.023. Epub 2010 Apr 1.
6
Hematopoietic stem cell origin of mesenchymal cells: opportunity for novel therapeutic approaches.造血干细胞起源的间充质细胞:新型治疗方法的机会。
Int J Hematol. 2010 Apr;91(3):353-9. doi: 10.1007/s12185-010-0554-4. Epub 2010 Mar 26.
7
MCP1 directs trafficking of hematopoietic stem cell-derived fibroblast precursors in solid tumor.MCP1 指导造血干细胞衍生的成纤维细胞前体在实体瘤中的运输。
Am J Pathol. 2010 Apr;176(4):1914-26. doi: 10.2353/ajpath.2010.080839. Epub 2010 Feb 18.
8
Hematopoietic stem cell origin of adipocytes.脂肪细胞的造血干细胞起源。
Exp Hematol. 2009 Sep;37(9):1108-20, 1120.e1-4. doi: 10.1016/j.exphem.2009.06.008. Epub 2009 Jul 2.
9
Repair of tissues by adult stem/progenitor cells (MSCs): controversies, myths, and changing paradigms.成体干细胞/祖细胞(间充质干细胞)对组织的修复:争议、误解及不断变化的范式
Mol Ther. 2009 Jun;17(6):939-46. doi: 10.1038/mt.2009.62. Epub 2009 Mar 31.
10
The therapeutic applications of multipotential mesenchymal/stromal stem cells in skeletal tissue repair.多能间充质/基质干细胞在骨骼组织修复中的治疗应用。
J Cell Physiol. 2009 Feb;218(2):237-45. doi: 10.1002/jcp.21592.

造血干细胞分化为成骨-软骨细胞。

Hematopoietic stem cells give rise to osteo-chondrogenic cells.

机构信息

Department of Veterans Affairs Medical Center, Ralph H. Johnson VAMC, Medical University of South Carolina, Charleston, SC, USA.

出版信息

Blood Cells Mol Dis. 2013 Jan;50(1):41-9. doi: 10.1016/j.bcmd.2012.08.003. Epub 2012 Sep 3.

DOI:10.1016/j.bcmd.2012.08.003
PMID:22954476
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3521579/
Abstract

Repair of bone fracture requires recruitment and proliferation of stem cells with the capacity to differentiate to functional osteoblasts. Given the close association of bone and bone marrow (BM), it has been suggested that BM may serve as a source of these progenitors. To test the ability of hematopoietic stem cells (HSCs) to give rise to osteo-chondrogenic cells, we used a single HSC transplantation paradigm in uninjured bone and in conjunction with a tibial fracture model. Mice were lethally irradiated and transplanted with a clonal population of cells derived from a single enhanced green fluorescent protein positive (eGFP+) HSC. Analysis of paraffin sections from these animals showed the presence of eGFP+ osteocytes and hypertrophic chondrocytes. To determine the contribution of HSC-derived cells to fracture repair, non-stabilized tibial fracture was created. Paraffin sections were examined at 7 days, 2 weeks and 2 months after fracture and eGFP+ hypertrophic chondrocytes, osteoblasts and osteocytes were identified at the callus site. These cells stained positive for Runx-2 or osteocalcin and also stained for eGFP demonstrating their origin from the HSC. Together, these findings strongly support the concept that HSCs generate bone cells and suggest therapeutic potentials of HSCs in fracture repair.

摘要

骨折修复需要募集和增殖具有分化为功能性成骨细胞能力的干细胞。鉴于骨骼和骨髓(BM)密切相关,有人认为 BM 可能是这些祖细胞的来源。为了测试造血干细胞(HSCs)产生成骨-软骨细胞的能力,我们在未受伤的骨骼中使用了单次 HSC 移植范例,并结合了胫骨骨折模型。小鼠接受致死性辐射,并移植了源自单个增强型绿色荧光蛋白阳性(eGFP+)HSC 的克隆群体细胞。对这些动物的石蜡切片进行分析显示存在 eGFP+骨细胞和成骨细胞。为了确定 HSC 衍生细胞对骨折修复的贡献,创建了非稳定胫骨骨折。在骨折后 7 天、2 周和 2 个月时检查石蜡切片,并在骨痂部位鉴定出 eGFP+肥大软骨细胞、成骨细胞和成骨细胞。这些细胞对 Runx-2 或骨钙素呈阳性染色,并且对 eGFP 也呈阳性染色,表明它们源自 HSC。这些发现共同强烈支持 HSCs 产生骨细胞的概念,并表明 HSCs 在骨折修复中的治疗潜力。