Blended Nanostructured Degradable Mesh with Endometrial Mesenchymal Stem Cells Promotes Tissue Integration and Anti-Inflammatory Response in Vivo for Pelvic Floor Application

被引:52
作者
Mukherjee, Shayanti [1 ,2 ,3 ]
Darzi, Saeedeh [1 ]
Rosamilia, Anna [2 ,4 ]
Kadam, Vinod [3 ]
Truong, Yen [3 ]
Werkmeister, Jerome A. [1 ,2 ,3 ]
Gargett, Caroline E. [1 ,2 ]
机构
[1] Hudson Inst Med Res, Ritchie Ctr, Clayton, Vic 3168, Australia
[2] Monash Univ, Dept Obstet & Gynaecol, Clayton, Vic 3168, Australia
[3] CSIRO Mfg, Clayton, Vic 3168, Australia
[4] Monash Hlth, Pelv Floor Disorders Unit, Clayton, Vic 3168, Australia
基金
英国医学研究理事会;
关键词
ORGAN PROLAPSE; COLLAGEN; IMPLANTS; GELATIN; THERAPY;
D O I
10.1021/acs.biomac.8b01661
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The current urogynecological clinical meshes trigger unfavorable foreign body response which leads to graft failure in the long term. To overcome the present challenge, we applied a tissue engineering strategy using endometrial SUSD2+ mesenchymal stem cells (eMSCs) with high regenerative properties. This study delves deeper into foreign body response to SUSD2+ eMSC based degradable PLACL/gelatin nanofiber meshes using a mouse model targeted at understanding immunomodulation and mesh integration in the long term. Delivery of cells with nanofiber mesh provides a unique topography that enables entrapment of therapeutic cells for up to 6 weeks that promotes substantial cellular infiltration of host anti-inflammatory macrophages. As a result, degradation rate and tissue integration are highly impacted by eMSCs, revealing an unexpected level of implant integration over 6 weeks in vivo. From a clinical perspective, such immunomodulation may aid in overcoming the current challenges and provide an alternative to an unmet women's urogynecological health need.
引用
收藏
页码:454 / 468
页数:15
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