A therapy-grade protocol for differentiation of pluripotent stem cells into mesenchymal stem cells using platelet lysate as supplement

被引:43
作者
Luzzani, Carlos [1 ]
Neiman, Gabriel [1 ]
Garate, Ximena [1 ]
Questa, Maria [1 ]
Solari, Claudia [2 ]
Fernandez Espinosa, Dario [1 ]
Garcia, Marcela [3 ]
Errecalde, Ana Lia [3 ]
Guberman, Alejandra [2 ,4 ]
Elida Scassa, Maria [1 ]
Emilio Sevlever, Gustavo [1 ]
Romorini, Leonardo [1 ,4 ]
Gabriel Miriuka, Santiago [1 ,3 ,4 ]
机构
[1] Fdn FLENI, CONICET, LIAN Unidad Asociada, Lab Biol Desarrollo Celular, Belen De Escobar, Argentina
[2] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Lab Regulac Expres Gen, Buenos Aires, DF, Argentina
[3] Univ Nacl La Plata, Fac Ciencias Med, Catedra Citol Histol & Embriol, RA-1900 La Plata, Argentina
[4] Consejo Nacl Invest Cient & Tecn, RA-1033 Buenos Aires, DF, Argentina
关键词
FETAL BOVINE SERUM; STROMAL CELLS; BONE-MARROW; IN-VITRO; EXPANSION; DERIVATION; MSCS; OCT4; VIVO; PROGENITORS;
D O I
10.1186/scrt540
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
Introduction: Mesenchymal stem cells (MSCs) are a promising source of cells for regenerative therapies. Although they can be isolated easily from several tissues, cell expansion is limited since their properties are lost with successive passages. Hence, pluripotent derived MSCs (PD-MSCs) arise as a suitable alternative for MSC production. Nevertheless, at present, PD-MSC derivation protocols are either expensive or not suitable for clinical purposes. Methods: In this work we present a therapy-grade, inexpensive and simple protocol to derive MSCs from pluripotent stem cells (PSCs) based on the use of platelet lysate (PL) as medium supplement. Results: We showed that the PD-MSCPL expressed multiple MSC markers, including CD90, CD73, CD105, CD166, and CD271, among others. These cells also show multilineage differentiation ability and immunomodulatory effects on pre-stimulated lymphocytes. Thorough characterization of these cells showed that a PD-MSCPL resembles an umbilical cord (UC) MSC and differs from a PSC in surface marker and extracellular matrix proteins and integrin expression. Moreover, the OCT-4 promoter is re-methylated with mesenchymal differentiation comparable with the methylation levels of UC-MSCs and fibroblasts. Lastly, the use of PL-supplemented medium generates significantly more MSCs than the use of fetal bovine serum. Conclusions: This protocol can be used to generate a large amount of PD-MSCs with low cost and is compatible with clinical therapies.
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页数:13
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