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DOI 10.2217/rme.14.92

Медицинская библиотека · Regenerative medicine · 2015

Multidifferentiation potential of human mesenchymal stem cells from adipose tissue and hamstring tendons for musculoskeletal cell-based therapy.

Stanco Deborah, Viganò Marco, Perucca Orfei Carlotta, Di Giancamillo Alessia, Peretti Giuseppe M, Lanfranchi Luciano, de Girolamo Laura

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

AIM: Adipose-derived stem cells (ASCs) have been deeply characterized for their usefulness in musculoskeletal tissue regeneration; recently, other mesenchymal stem cell (MSC) sources have also been proposed. This study compares for the first time human tendon stem/progenitor cells isolated from hamstring tendons with human ASCs.

MATERIALS &

METHODS

Human TSPCs and ASCs were isolated from hamstring tendon portions and adipose tissue of healthy donors undergoing ACL reconstruction or liposuction, respectively (n = 7). Clonogenic ability, immunophenotype and multi-differentiation potential were assessed and compared.

RESULTS

Both populations showed similar proliferation and clonogenic ability and expressed embryonic stem cell genes and MSC surface markers. Tendon stem/progenitor cells showed lower adipogenic and osteogenic ability, but after the chondrogenic differentiation, they produced more abundant glycosaminoglycans and expressed higher levels of aggrecan with regards to ASCs. The tenogenic induction with BMP-12 upregulated SCX and DCN gene expression in both populations.

CONCLUSION

Our results demonstrate that waste hamstring tendon fragments could represent a convenient MSC source for musculoskeletal regenerative medicine.

Для цитирования: Stanco Deborah, Viganò Marco, Perucca Orfei Carlotta, Di Giancamillo Alessia, Peretti Giuseppe M, Lanfranchi Luciano, de Girolamo Laura. Multidifferentiation potential of human mesenchymal stem cells from adipose tissue and hamstring tendons for musculoskeletal cell-based therapy.. Regenerative medicine. 2015. DOI: 10.2217/rme.14.92.

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