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

Gesine Kögler(Heinrich Heine University Düsseldorf), Sandra Sensken(Heinrich Heine University Düsseldorf), Judith A. Airey(University of Nevada, Reno), Thorsten Trapp(Heinrich Heine University Düsseldorf), Markus Müschen(Heinrich Heine University Düsseldorf), Niklas Feldhahn(Heinrich Heine University Düsseldorf), Stefanie Liedtke(Heinrich Heine University Düsseldorf), Rüdiger V. Sorg(Heinrich Heine University Düsseldorf), Johannes Fischer(Heinrich Heine University Düsseldorf), Claudia Rosenbaum, Susanne Greschat, A. Knipper(Heinrich Heine University Düsseldorf), Jörg Bender, Özer Degistirici(Heinrich Heine University Düsseldorf), Jizong Gao(Case Western Reserve University), Arnold I. Caplan(Case Western Reserve University), Evan Colletti(University of Nevada, Reno), Graça Almeida‐Porada(University of Nevada, Reno), Hans Werner Müller, Esmail D. Zanjani(University of Nevada, Reno), Peter Wernet(Heinrich Heine University Düsseldorf)
The Journal of Experimental Medicine
July 19, 2004
Cited by 1,028Open Access
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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 10(15) 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.


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