Blended Nanostructured Degradable Mesh with Endometrial Mesenchymal Stem Cells Promotes Tissue Integration and Anti-Inflammatory Response in Vivo for Pelvic Floor Application.
Shayanti MukherjeeSaeedeh DarziAnna RosamiliaVinod KadamYen Bach TruongJerome A WerkmeisterCaroline E GargettPublished in: Biomacromolecules (2018)
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.
Keyphrases
- mesenchymal stem cells
- tissue engineering
- induced apoptosis
- inflammatory response
- umbilical cord
- mouse model
- cell cycle arrest
- anti inflammatory
- stem cells
- healthcare
- bone marrow
- cell therapy
- public health
- mental health
- polycystic ovary syndrome
- endometrial cancer
- type diabetes
- signaling pathway
- gestational age
- cancer therapy
- climate change
- pregnant women
- immune response
- adipose tissue
- cell proliferation
- hyaluronic acid
- skeletal muscle
- lps induced