Transplantation of collagen scaffold with autologous bone marrow mononuclear cells promotes functional endometrium reconstruction via downregulating ΔNp63 expression in Asherman's syndrome

被引:2
作者
Guangfeng Zhao [1 ]
Yun Cao [1 ]
Xianghong Zhu [1 ]
Xiaoqiu Tang [1 ]
Lijun Ding [2 ]
Haixiang Sun [2 ]
Juan Li [1 ]
Xinan Li [1 ]
Chenyan Dai [1 ]
Tong Ru [1 ]
Hui Zhu [1 ]
Jingjie Lu [1 ]
Caimei Lin [1 ]
Jingmei Wang [3 ]
Guijun Yan [2 ]
Huiyan Wang [1 ]
Lei Wang [1 ]
Yimin Dai [1 ]
Bin Wang [4 ]
Ruotian Li [5 ]
Jianwu Dai [6 ]
Yan Zhou [7 ]
Yali Hu [1 ]
机构
[1] Department of Obstetrics and Gynecology, The Affiliated Drum Tower Hospital of Nanjing University Medical School
[2] Center for Reproductive Medicine, Department of Obstetrics and Gynecology, The Affiliated Drum Tower Hospital of Nanjing University Medical School
[3] Department of Pathology, The Affiliated Drum Tower Hospital of Nanjing University Medical School
[4] Nanjing Center for Stem Cells and Biomaterials, The Affiliated Drum Tower Hospital of Nanjing University Medical School
[5] The Affiliated Drum Tower Hospital of Nanjing University Medical School
[6] Institute of Genetics and Developmental Biology, Chinese Academy of Sciences
[7] Department of Obstetrics, Gynecology and Reproductive Sciences, Center for Reproductive Sciences, Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California San Francisco
基金
中国国家自然科学基金;
关键词
Asherman’s syndrome; ΔNp63; quiescence; endometrial regeneration; bone marrow stem cell based therapy;
D O I
暂无
中图分类号
R711.74 [子宫及子宫颈疾病];
学科分类号
100211 ;
摘要
Asherman’s syndrome(AS) is a common disease that presents endometrial regeneration disorder. However, little is known about its molecular features of this aregenerative endometrium in AS and how to reconstruct the functioning endometrium for the patients with AS. Here, we report that ΔNp63 is significantly upregulated in residual epithelial cells of the impaired endometrium in AS; the upregulated-ΔNp63 induces endometrial quiescence and alteration of stemness. Importantly, we demonstrate that engrafting high density of autologous bone marrow mononuclear cells(BMNCs) loaded in collagen scaffold onto the uterine lining of patients with AS downregulates ΔNp63 expression, reverses ΔNp63-induced pathological changes, normalizes the stemness alterations and restores endometrial regeneration. Finally, five patients achieved successful pregnancies and live births. Therefore, we conclude that ΔNp63 is a crucial therapeutic target for AS. This novel treatment significantly improves the outcome for the patients with severe AS.
引用
收藏
页码:404 / 416
页数:13
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