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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Mesenchymal stem cell-mediated ectopic hematopoiesis alleviates aging-related phenotype in immunocompromised mice.
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Mesenchymal stem cell-mediated ectopic hematopoiesis alleviates aging-related phenotype in immunocompromised mice.

机译:间充质干细胞介导的异位造血功能减轻了免疫受损小鼠的衰老相关表型。

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Subcutaneous transplants of bone marrow mesenchymal stem cells (BMMSCs) are capable of generating ectopic bone and organizing functional hematopoietic marrow elements in animal models. Here we report that immunocompromised mice received subcutaneous BMMSC transplants using hydroxyapatite tricalcium phosphate as a carrier suppressed age-related degeneration in multiple organs and benefited an increase in life span extension compared with control littermates. The newly organized ectopic bone/marrow system restores active hematopoiesis via the erythropoietin receptor/signal transducer and activator of transcription 5 (Stat5) pathway. Furthermore, the BMMSC recipient mice showed elevated level of Klotho and suppression of insulin-like growth factor I signaling, which may be the mechanism contributing to the alleviation of aging-like phenotypes and prolongation of life in the treated mice. This work reveals that erythropoietin receptor/Stat5 pathway contributes to BMMSC-organized ectopic hematopoiesis, which may offer a treatment paradigm of reversing age-related degeneration of multiple organs in adult immunocompromised mice.
机译:骨髓间充质干细胞(BMMSC)的皮下移植能够在动物模型中生成异位骨并组织功能性造血骨髓元件。在这里,我们报告免疫受损的小鼠接受使用羟基磷灰石磷酸三钙作为载体的皮下BMMSC移植,抑制了多个器官中与年龄相关的变性,并且与对照同窝仔相比,寿命延长了。新组织的异位骨/骨髓系统通过促红细胞生成素受体/信号转导子和转录激活子5(Stat5)途径恢复了活跃的造血功能。此外,BMMSC受体小鼠表现出升高的Klotho水平和胰岛素样生长因子I信号转导的抑制,这可能是减轻所治疗小鼠的衰老样表型和延长寿命的机制。这项工作表明促红细胞生成素受体/ Stat5通路有助于BMMSC组织的异位造血,这可能为逆转成年免疫受损小鼠的多器官衰老引起的变性提供了治疗范例。

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