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Studies On Anticancer Activity Of Silver Nanoparticles And Its Role In Enhancing Anticancer Activity Of Phophamide | 5170
ISSN: 2157-7013

Journal of Cell Science & Therapy
Open Access

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Studies on anticancer activity of silver nanoparticles and its role in enhancing anticancer activity of phophamide

International Conference & Exhibition on Cell Science & Stem Cell Research

Rebecca Thombre, Sourabh Mehta and Shubhangi Puranik

ScientificTracks Abstracts: J Cell Sci Ther

DOI: 10.4172/2157-7013.S1.02

Human parthenogenetic stem cells (hpSC) are pluripotent stem cells derived from unfertilized oozytes. hpSC behave the same way as human embryonic stem cells (hESC) in their proliferation capacity and multilineage diff erentiation in vitro. hpSC can be either heterozygous or homozygous. Homozygous hpSC have the potential to serve as a useful source of cells in clinical therapy because if the HLA type is common, their diff erentiated derivatives can match millions of individuals. In addition, hpSC do not raise the same ethical concerns as conventional hESC because the generation of hpSC does not involve the destruction of a viable human embryo. Together these two advantages make hpSC a very promising source of various diff erentiated somatic cell lines including multipotent neuronal cells (NC). In this study we derive NC from hpSC using an approach based on the adherent model with modifi cations. Rosettes of neuroepithelial cells were formed by culturing hpSC in feeder-free conditions with no serum and high concentration of bFGF. Th e rosettes were then isolated, dissociated into single cell suspension, and propagated as an adherent cell culture leading to human parthenogenetic NC (hpNC). Th e hpNC can be propagated for up to 30 passages and express the neural markers NES (Nestin), SOX2, and MSI1 (Musashi-1) as determined by qRT- PCR and immunocytochemistry. Expression of OCT4 was not detected at the RNA and protein levels. hpNC can be further diff erentiated into neurons and glia. Th e hpNC derived neurons express TUBB3 (Tubulin beta III) and MAP2 and elicit action potentials and outward, and inward currents.
R uslan Semechkin, Ph.D., is Vice President, Head of Neurology Division of International Stem Cell Corporation. Dr. Semechkin was trained in medical genetics, physiology and stem cell biology and holds his M.S. degree from Faculty of Fundamental Medicine of Moscow State University. He earned his Ph.D. degree in physiology from Anokhin Research Institute, Russian Academy of Medical Sciences. Dr. Semechkin has lectured on stem cell biology, including the use of stem cells for neurology and skin regeneration. He has publications in the fi eld of clinical and molecular biology, and is author of various patent applications.
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