Tissue-engineering with muscle fiber fragments improves the strength of a weak abdominal wall in rats View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2016-08-16

AUTHORS

Hanna Jangö, Søren Gräs, Lise Christensen, Gunnar Lose

ABSTRACT

Introduction and hypothesisAlternative approaches to reinforce the native tissue in patients with pelvic organ prolapse (POP) are needed to improve surgical outcome. Our aims were to develop a weakened abdominal wall in a rat model to mimic the weakened vaginal wall in women with POP and then evaluate the regenerative potential of a quickly biodegradable synthetic scaffold, methoxypolyethylene glycol polylactic-co-glycolic acid (MPEG-PLGA), seeded with autologous muscle fiber fragments (MFFs) using this model.MethodsIn an initial pilot study with 15 animals, significant weakening of the abdominal wall and a feasible technique was established by creating a partial defect with removal of one abdominal muscle layer. Subsequently, 18 rats were evenly divided into three groups: (1) unrepaired partial defect; (2) partial defect repaired with MPEG-PLGA; (3) partial defect repaired with MPEG-PLGA and MFFs labeled with PKH26-fluorescence dye. After 8 weeks, we performed histopathological and immunohistochemical testing, fluorescence analysis, and uniaxial biomechanical testing.ResultsBoth macroscopically and microscopically, the MPEG-PLGA scaffold was fully degraded, with no signs of an inflammatory or foreign-body response. PKH26-positive cells were found in all animals from the group with added MFFs. Analysis of variance (ANOVA) showed a significant difference between groups with respect to load at failure (p = 0.028), and post hoc testing revealed that the group with MPEG-PLGA and MFFs showed a significantly higher strength than the group with MPEG-PLGA alone (p = 0.034).ConclusionTissue-engineering with MFFs seeded on a scaffold of biodegradable MPEG-PLGA might be an interesting adjunct to future POP repair. More... »

PAGES

223-229

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00192-016-3091-8

DOI

http://dx.doi.org/10.1007/s00192-016-3091-8

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1038350199

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/27530522


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