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CD30 Receptor-Targeted Lentiviral Vectors for Human Induced Pluripotent Stem Cell-Specific Gene Modification.
Friedel, Thorsten; Jung-Klawitter, Sabine; Sebe, Attila; Schenk, Franziska; Modlich, Ute; Ivics, Zoltán; Schumann, Gerald G; Buchholz, Christian J; Schneider, Irene C.
Affiliation
  • Friedel T; 1 Molecular Biotechnology and Gene Therapy, Paul-Ehrlich-Institut , Langen, Germany .
  • Jung-Klawitter S; 2 Medical Biotechnology, Paul-Ehrlich-Institut , Langen, Germany .
  • Sebe A; 2 Medical Biotechnology, Paul-Ehrlich-Institut , Langen, Germany .
  • Schenk F; 3 Research Group for Gene Modification in Stem Cells, LOEWE Center of Cell and Gene Therapy Frankfurt , Paul-Ehrlich-Institut, Langen, Germany .
  • Modlich U; 3 Research Group for Gene Modification in Stem Cells, LOEWE Center of Cell and Gene Therapy Frankfurt , Paul-Ehrlich-Institut, Langen, Germany .
  • Ivics Z; 2 Medical Biotechnology, Paul-Ehrlich-Institut , Langen, Germany .
  • Schumann GG; 2 Medical Biotechnology, Paul-Ehrlich-Institut , Langen, Germany .
  • Buchholz CJ; 1 Molecular Biotechnology and Gene Therapy, Paul-Ehrlich-Institut , Langen, Germany .
  • Schneider IC; 1 Molecular Biotechnology and Gene Therapy, Paul-Ehrlich-Institut , Langen, Germany .
Stem Cells Dev ; 25(9): 729-39, 2016 05 01.
Article in En | MEDLINE | ID: mdl-26956718
ABSTRACT
Cultures of induced pluripotent stem cells (iPSCs) often contain cells of varying grades of pluripotency. We present novel lentiviral vectors targeted to the surface receptor CD30 (CD30-LV) to transfer genes into iPSCs that are truly pluripotent as demonstrated by marker gene expression. We demonstrate that CD30 expression is restricted to SSEA4(high) cells of human iPSC cultures and a human embryonic stem cell line. When CD30-LV was added to iPSCs during routine cultivation, efficient and exclusive transduction of cells positive for the pluripotency marker Oct-4 was achieved, while retaining their pluripotency. When added during the reprogramming process, CD30-LV solely transduced cells that became fully reprogrammed iPSCs as confirmed by co-expression of endogenous Nanog and the reporter gene. Thus, CD30-LV may serve as novel tool for the selective gene transfer into PSCs with broad applications in basic and therapeutic research.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Therapy / Ki-1 Antigen / Lentivirus / Induced Pluripotent Stem Cells / Genetic Vectors Limits: Humans Language: En Journal: Stem Cells Dev Journal subject: HEMATOLOGIA Year: 2016 Document type: Article Affiliation country: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Therapy / Ki-1 Antigen / Lentivirus / Induced Pluripotent Stem Cells / Genetic Vectors Limits: Humans Language: En Journal: Stem Cells Dev Journal subject: HEMATOLOGIA Year: 2016 Document type: Article Affiliation country: Germany