Your browser doesn't support javascript.
loading
Dispase/collagenase cocktail allows for coisolation of satellite cells and fibroadipogenic progenitors from human skeletal muscle.
Balayan, Alis; DeBoutray, Marie; Molley, Thomas G; Ruoss, Severin; Maceda, Matthew; Sevier, Ashley; Robertson, Catherine M; Ward, Samuel R; Engler, Adam J.
Afiliación
  • Balayan A; Biomedical Sciences Program, UC San Diego, La Jolla, California, United States.
  • DeBoutray M; Department of ENT and Maxillofacial Surgery, Montpellier University, Montpellier, France.
  • Molley TG; Chien-Lay Department of Bioengineering, UC San Diego, La Jolla, California, United States.
  • Ruoss S; Department of Orthopaedic Surgery, UC San Diego, La Jolla, California, United States.
  • Maceda M; Department of Orthopaedic Surgery, UC San Diego, La Jolla, California, United States.
  • Sevier A; California State University, Bakersfield, Bakersfield, California, United States.
  • Robertson CM; Department of Orthopaedic Surgery, UC San Diego, La Jolla, California, United States.
  • Ward SR; Department of Orthopaedic Surgery, UC San Diego, La Jolla, California, United States.
  • Engler AJ; Department of Radiology, UC San Diego, La Jolla, California, United States.
Am J Physiol Cell Physiol ; 326(4): C1193-C1202, 2024 04 01.
Article en En | MEDLINE | ID: mdl-38581669
ABSTRACT
Satellite cells (SCs) and fibroadipogenic progenitors (FAPs) are progenitor populations found in muscle that form new myofibers postinjury. Muscle development, regeneration, and tissue-engineering experiments require robust progenitor populations, yet their isolation and expansion are difficult given their scarcity in muscle, limited muscle biopsy sizes in humans, and lack of methodological detail in the literature. Here, we investigated whether a dispase and collagenase type 1 and 2 cocktail could allow dual isolation of SCs and FAPs, enabling significantly increased yield from human skeletal muscle. Postdissociation, we found that single cells could be sorted into CD56 + CD31-CD45- (SC) and CD56-CD31-CD45- (FAP) cell populations, expanded in culture, and characterized for lineage-specific marker expression and differentiation capacity; we obtained ∼10% SCs and ∼40% FAPs, with yields twofold better than what is reported in current literature. SCs were PAX7+ and retained CD56 expression and myogenic fusion potential after multiple passages, expanding up to 1012 cells. Conversely, FAPs expressed CD140a and differentiated into either fibroblasts or adipocytes upon induction. This study demonstrates robust isolation of both SCs and FAPs from the same muscle sample with SC recovery more than two times higher than previously reported, which could enable translational studies for muscle injuries.NEW & NOTEWORTHY We demonstrated that a dispase/collagenase cocktail allows for simultaneous isolation of SCs and FAPs with 2× higher SC yield compared with other studies. We provide a thorough characterization of SC and FAP in vitro expansion that other studies have not reported. Following our dissociation, SCs and FAPs were able to expand by up to 1012 cells before reaching senescence and maintained differentiation capacity in vitro demonstrating their efficacy for clinical translation for muscle injury.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Endopeptidasas / Músculo Esquelético / Células Satélite del Músculo Esquelético Límite: Humans Idioma: En Revista: Am J Physiol Cell Physiol Asunto de la revista: FISIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Endopeptidasas / Músculo Esquelético / Células Satélite del Músculo Esquelético Límite: Humans Idioma: En Revista: Am J Physiol Cell Physiol Asunto de la revista: FISIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos