IMT504, the Prototype of the Immunostimulatory Oligonucleotides of the PyNTTTTGT Class, Increases the Number of Progenitors of Mesenchymal Stem Cells Both In Vitro and In Vivo: Potential Use in Tissue Repair Therapy
Autor: | Andres Clemente Hernando Insua, Juan Fló, Ricardo A. López, Norma Alejandra Chasseing, Juan M. Rodríguez, Alejandro D. Montaner, Jorge Zorzopulos, Erica Leonor Hofer, Fernanda Elías |
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Rok vydání: | 2007 |
Předmět: |
Male
CIENCIAS MÉDICAS Y DE LA SALUD LEUCOCYTES Bone Marrow Cells Bone healing Biology Non-CpG OLIGONUCLEOTIDES Biotecnología de la Salud Colony-Forming Units Assay Rats Sprague-Dawley Ciencias Biológicas TISSUE REPAIR THERAPY Biología Celular Microbiología In vivo medicine Animals Progenitor cell Fibroblast Cells Cultured IMT504 Base Sequence Mesenchymal stem cell Cell Differentiation Mesenchymal Stem Cells MESENCHYMAL STEM CELLS Cell Biology Molecular biology In vitro Rats medicine.anatomical_structure Oligodeoxyribonucleotides Cell culture Immunology Leukocytes Mononuclear Molecular Medicine Bone marrow Cell Division CIENCIAS NATURALES Y EXACTAS Stem Cell Transplantation Otras Biotecnologías de la Salud Developmental Biology |
Zdroj: | Stem Cells. 25:1047-1054 |
ISSN: | 1549-4918 1066-5099 |
Popis: | Bone marrow (BM)-derived adult mesenchymal stem cells (MSCs) have the capacity to differentiate in vitro into different cell lines. This makes them a likely source for application in tissue repair therapies. Here, we report evidence indicating that, both in vivo and in vitro, IMT504, the prototype of the PyNTTTTGT class of immunostimulatory oligonucleotides, significantly increases the number of fibroblast colony-forming units (CFU-Fs) that originate MSCs. When rat BM cells were cultured with IMT504, the mean number of CFU-Fs increased about three times as compared with untreated controls (CFU-F: 19 +/- 6.3 vs. 6.8 +/- 2.0/2 x 10(6) seeded BM cells, p = .03). Furthermore, rats inoculated with IMT504 had a significantly higher number of CFU-Fs both in BM (CFU-F: 124 +/- 33 vs. 38 +/- 17/femur, p = .04) and in peripheral blood (animals with detectable CFU-Fs in circulation 8/12 vs. 2/12, p = .04) as compared with untreated animals. On the other hand, BM-derived adherent cells either treated in vitro with IMT504 or obtained from animals injected with IMT504 possess the capacity to differentiate to the osteogenic and adipogenic cell lineages as regular MSCs. Finally, we found that repair of a bone defect was accelerated in rats injected with IMT504 as compared with control animals (area with consolidated bone: 80% +/- 6.4% vs. 49% +/- 3.5%, p = .03, n = 10 rats per group). Importantly, when two human BM were cultured in the presence of IMT504, the mean number of fibroblastic adherent colonies also increased as compared with controls. These results suggest the possibility of clinical use of IMT504 in bone, and presumably other, tissue repair therapies. Fil: Hernando Insúa, Andrés. Immunotech S.a.; Argentina Fil: Montaner, Alejandro Daniel. Fundación Pablo Cassara; Argentina Fil: Rodriguez, Juan Manuel. Immunotech S.a.; Argentina Fil: Elías, Fernanda. Immunotech S.a.; Argentina Fil: Fló, Juan. Immunotech S.a.; Argentina Fil: López, Ricardo A.. Immunotech S.a.; Argentina Fil: Zorzopulos, Ricardo A.. Immunotech S.a.; Argentina Fil: Hofer, Erica L.. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina Fil: Chasseing, Norma Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina |
Databáze: | OpenAIRE |
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