A New Human Somatic Stem Cell from Placental Cord Blood with Intrinsic Pluripotent Differentiation Potential

Author:

Kögler Gesine1,Sensken Sandra1,Airey Judith A.2,Trapp Thorsten1,Müschen Markus1,Feldhahn Niklas1,Liedtke Stefanie1,Sorg Rüdiger V.1,Fischer Johannes1,Rosenbaum Claudia3,Greschat Susanne3,Knipper Andreas14,Bender Jörg4,Degistirici Özer14,Gao Jizong5,Caplan Arnold I.5,Colletti Evan J.2,Almeida-Porada Graça6,Müller Hans W.3,Zanjani Esmail6,Wernet Peter1

Affiliation:

1. Institute for Transplantation Diagnostics and Cell Therapeutics, University of Düsseldorf Medical School, 40225 Düsseldorf, Germany

2. Department of Pharmacology, University of Nevada Medical School, Reno, NV 89523

3. Molecular Neurobiology Laboratory, Department of Neurology, University of Düsseldorf Medical School, 40225 Düsseldorf, Germany

4. Kourion Therapeutics, 40764 Langenfeld, Germany

5. Skeletal Research Center, Case Western Reserve University, Cleveland, OH 44106

6. Veterans Administration Medical Center, University of Nevada, Reno, NV 89557

Abstract

Here a new, intrinsically pluripotent, CD45-negative population from human cord blood, termed unrestricted somatic stem cells (USSCs) is described. This rare population grows adherently and can be expanded to 1015 cells without losing pluripotency. In vitro USSCs showed homogeneous differentiation into osteoblasts, chondroblasts, adipocytes, and hematopoietic and neural cells including astrocytes and neurons that express neurofilament, sodium channel protein, and various neurotransmitter phenotypes. Stereotactic implantation of USSCs into intact adult rat brain revealed that human Tau-positive cells persisted for up to 3 mo and showed migratory activity and a typical neuron-like morphology. In vivo differentiation of USSCs along mesodermal and endodermal pathways was demonstrated in animal models. Bony reconstitution was observed after transplantation of USSC-loaded calcium phosphate cylinders in nude rat femurs. Chondrogenesis occurred after transplanting cell-loaded gelfoam sponges into nude mice. Transplantation of USSCs in a noninjury model, the preimmune fetal sheep, resulted in up to 5% human hematopoietic engraftment. More than 20% albumin-producing human parenchymal hepatic cells with absence of cell fusion and substantial numbers of human cardiomyocytes in both atria and ventricles of the sheep heart were detected many months after USSC transplantation. No tumor formation was observed in any of these animals.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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