Human and murine amniotic fluid c-Kit+Lin− cells display hematopoietic activity

Author:

Ditadi Andrea123,de Coppi Paolo34,Picone Olivier567,Gautreau Laetitia28,Smati Rim28,Six Emmanuelle12,Bonhomme Delphine12,Ezine Sophie28,Frydman René567,Cavazzana-Calvo Marina129,André-Schmutz Isabelle12

Affiliation:

1. Inserm U768, Paris, France;

2. Faculty of Medicine, University of Paris René Descartes, IFR94, Paris, France;

3. Stem Cell Processing Laboratory, Department of Pediatrics, University of Padua, Padua, Italy;

4. Surgery Unit, UCL Institute of Child Health and Great Ormond Street Hospital, London, United Kingdom;

5. Assistance Publique-Hopitaux de Paris, Gynecology & Obstetrics Department, Antoine Béclère Hospital, Clamart, France;

6. University of Paris-Sud, Clamart, France;

7. Inserm U782, Clamart, France;

8. Inserm U591, Paris, France; and

9. Biotherapy Department, Assistance Publique-Hopitaux de Paris, Necker Children's Hospital, Paris, France

Abstract

AbstractWe have isolated c-Kit+Lin− cells from both human and murine amniotic fluid (AF) and investigated their hematopoietic potential. In vitro, the c-Kit+Lin− population in both species displayed a multilineage hematopoietic potential, as demonstrated by the generation of erythroid, myeloid, and lymphoid cells. In vivo, cells belonging to all 3 hematopoietic lineages were found after primary and secondary transplantation of murine c-Kit+Lin− cells into immunocompromised hosts, thus demonstrating the ability of these cells to self-renew. Gene expression analysis of c-Kit+ cells isolated from murine AF confirmed these results. The presence of cells with similar characteristics in the surrounding amnion indicates the possible origin of AF c-Kit+Lin− cells. This is the first report showing that cells isolated from the AF do have hematopoietic potential; our results support the idea that AF may be a new source of stem cells for therapeutic applications.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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