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Lipidomics of mesenchymal stem cell differentiation.
Silva, Camila Gonzaga da; Barretto, Letícia Siqueira de Sá; Lo Turco, Edson Guimarães; Santos, Alex de Lima; Lessio, Camila; Martins Júnior, Helio Alves; Almeida, Fernando Gonçalves de.
Afiliación
  • Silva CGD; Department of Surgery, Division of Urology, Federal University of São Paulo, Rua Embaú 231- Vila Clementino, São Paulo, SP, 04039-060, Brazil.
  • Barretto LSS; Department of Surgery, Division of Urology, Federal University of São Paulo, Rua Embaú 231- Vila Clementino, São Paulo, SP, 04039-060, Brazil. Electronic address: leticiabarretto@hotmail.com.
  • Lo Turco EG; Department of Surgery, Division of Urology, Federal University of São Paulo, Rua Embaú 231- Vila Clementino, São Paulo, SP, 04039-060, Brazil.
  • Santos AL; Department of Surgery, Division of Urology, Federal University of São Paulo, Rua Embaú 231- Vila Clementino, São Paulo, SP, 04039-060, Brazil.
  • Lessio C; Department of Surgery, Division of Urology, Federal University of São Paulo, Rua Embaú 231- Vila Clementino, São Paulo, SP, 04039-060, Brazil.
  • Martins Júnior HA; SCIEX, Rua Júlio González, 132, Barra Funda, São Paulo, SP, 01156-060, Brazil.
  • Almeida FG; Department of Surgery, Division of Urology, Federal University of São Paulo, Rua Embaú 231- Vila Clementino, São Paulo, SP, 04039-060, Brazil.
Chem Phys Lipids ; 232: 104964, 2020 10.
Article en En | MEDLINE | ID: mdl-32882223
Mesenchymal stem cells (MSCs), such as adipose-derived stem cells (ADSCs) and skeletal muscle-derived stem cells (MDSCs), are potential sources for cell-based therapeutic strategies. However, there is little knowledge about the lipid composition of these stem cells and the mechanisms of their differentiation. Lipids have important biological and physiological functions that are critical for understanding the regulation and control of stem cell fate. This study sought to analyze the lipidome of rabbit ADSCs and MDSCs and their adipogenic and osteogenic differentiation. The MSCs were isolated and were characterized by flow cytometry. Lipids were extracted from both MSCs and differentiated cells, and the lipids were subsequently analyzed with a hybrid triple quadrupole time-of-flight mass spectrometer. The results showed a total of 1687 lipid species. MSCs exhibited different lipid profiles as well as changes in lipid composition after differentiation. Furthermore, the expression levels of N-acyl-phosphatidylethanolamine (NAPE) 54:7+NH4 (-FA 17:0(NH4)) and phosphatidylcholine (PC) 42:6+Na were higher in the adipogenic lineages in of both MSC types, and NAPE 58:2+NH4 (-FA 17:0 (NH4)) and NAPE 56:2+NH4 (-FA 17:0 (NH4)) had higher levels in the osteogenic lineages, suggesting lipid similarities in cells differentiated from different stem cell sources.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Diferenciación Celular / Células Madre Mesenquimatosas / Lipidómica Límite: Animals Idioma: En Revista: Chem Phys Lipids Año: 2020 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Diferenciación Celular / Células Madre Mesenquimatosas / Lipidómica Límite: Animals Idioma: En Revista: Chem Phys Lipids Año: 2020 Tipo del documento: Article País de afiliación: Brasil