Neurogenic differentiation of human dental stem cells in vitro
1
조회
0
다운로드
0
인용
0
참고문헌
키워드
초록
Objectives: The purpose of this study was to investigate the neurogenic differentiation of human dental pulp stem cells (DPSCs), periodontal ligamentstem cells (PDLSCs), and stem cells from apical papilla (SCAP). Materials and Methods: After induction of neurogenic differentiation using commercial differentiation medium, expression levels of neural markers,microtubule-associated protein 2 (MAP2), class III β-tubulin, and glial fibrillary acidic protein (GFAP) were identified using reverse transcriptase polymerase chain reaction (PCR), real-time PCR, and immunocytochemistry. Results: The induced cells showed neuron-like morphologies, similar to axons, dendrites, and perikaryons, which are composed of neurons in DPSCs, PDLSCs, and SCAP. The mRNA levels of neuronal markers tended to increase in differentiated cells. The expression of MAP2 and β-tubulin III also increased at the protein level in differentiation groups, even though GFAP was not detected via immunocytochemistry. Conclusion: Human dental stem cells including DPSCs, PDLSCs, and SCAP may have neurogenic differentiation capability in vitro. The presented data support the use of human dental stem cells as a possible alternative source of stem cells for therapeutic utility in the treatment of neurological diseases.
Abstract
Objectives: The purpose of this study was to investigate the neurogenic differentiation of human dental pulp stem cells (DPSCs), periodontal ligamentstem cells (PDLSCs), and stem cells from apical papilla (SCAP). Materials and Methods: After induction of neurogenic differentiation using commercial differentiation medium, expression levels of neural markers,microtubule-associated protein 2 (MAP2), class III β-tubulin, and glial fibrillary acidic protein (GFAP) were identified using reverse transcriptase polymerase chain reaction (PCR), real-time PCR, and immunocytochemistry. Results: The induced cells showed neuron-like morphologies, similar to axons, dendrites, and perikaryons, which are composed of neurons in DPSCs, PDLSCs, and SCAP. The mRNA levels of neuronal markers tended to increase in differentiated cells. The expression of MAP2 and β-tubulin III also increased at the protein level in differentiation groups, even though GFAP was not detected via immunocytochemistry. Conclusion: Human dental stem cells including DPSCs, PDLSCs, and SCAP may have neurogenic differentiation capability in vitro. The presented data support the use of human dental stem cells as a possible alternative source of stem cells for therapeutic utility in the treatment of neurological diseases.
참고문헌 (24)
- Duan X, "Application of induced pluripotent stem (iPS) cells in periodontal tissue regeneration", J Cell Physiol, 226, pp.150~157 (2011)
- Gimble JM, "Adipose-derived stem cells for regenerative medicine", Circ Res, 100, pp.1249~1260 (2007)
- Jones E, "Mesenchymal stem cells and bone regeneration: current status", Injury, 42, pp.562~568 (2011)
- Malliaras K, "Cardiac cell therapy: where we've been, where we are, and where we should be headed", Br Med Bull, 98, pp.161~185 (2011)
- Ohba S, "Identification of a potent combination of osteogenic genes for bone regeneration using embryonic stem (ES) cell-based sensor", FASEB J, 21, pp.1777~1787 (2007)
- Dangaria SJ, "Extracellular matrix-mediated differentiation of periodontal progenitor cells", Differentiation, 78, pp.79~90 (2009)
- Gronthos S, "Postnatal human dental pulp stem cells (DPSCs) in vitro and in vivo", Proc Natl Acad Sci USA, 97, pp.13625~13630 (2000)
- Miura M, "SHED: stem cells from human exfoliated deciduous teeth", Proc Natl Acad Sci USA, 100, pp.5807~5812 (2003)
- Seo BM, "Investigation of multipotent postnatal stem cells from human periodontal ligament", Lancet, 364, pp.149~155 (2004)
- Lee JH, "Effects of VEGF and FGF-2 on proliferation and differentiation of human periodontal ligament stem cells", Cell Tissue Res, 348, pp.475~484 (2012)
- Um S, "Effect of leptin on differentiation of human dental stem cells", Oral Dis, 17, pp.662~669 (2011)
- Sonoyama W, "Mesenchymal stem cell-mediated functional tooth regeneration in swine", PLoS One, 1, pp.e79~ (2006)
- Komada Y, "Origins and properties of dental, thymic, and bone marrow mesenchymal cells and their stem cells", PLoS One, 7, pp.e46436~ (2012)
- Chai Y, "Fate of the mammalian cranial neural crest during tooth and mandibular morphogenesis", Development, 127, pp.1671~1679 (2000)
- Abe S, "Neural crest stem cell property of apical pulp cells derived from human developing tooth", Cell Biol Int, 36, pp.927~936 (2012)
- Karaöz E, "Human dental pulp stem cells demonstrate better neural and epithelial stem cell properties than bone marrow-derived mesenchymal stem cells", Histochem Cell Biol, 136, pp.455~473 (2011)
- Kim SU, "Stem cell-based cell therapy in neurological diseases: a review", J Neurosci Res, 87, pp.2183~2200 (2009)
- Völlner F, "A two-step strategy for neuronal differentiation in vitro of human dental follicle cells", Differentiation, 77, pp.433~441 (2009)
- Nourbakhsh N, "Induced in vitro differentiation of neural-like cells from human exfoliated deciduous teeth-derived stem cells", Int J Dev Biol, 55, pp.189~195 (2011)
- Aanismaa R, "Human dental pulp stem cells differentiate into neural precursors but not into mature functional neurons", Stem Cell Discovery, 2, pp.85~91 (2012)
- Sakai K, "Human dental pulp-derived stem cells promote locomotor recovery after complete transection of the rat spinal cord by multiple neuro-regenerative mechanisms", J Clin Invest, 122, pp.80~90 (2012)
- de Almeida FM, "Human dental pulp cells: a new source of cell therapy in a mouse model of compressive spinal cord injury", J Neurotrauma, 28, pp.1939~1949 (2011)
- Nosrat IV, "Dental pulp cells provide neurotrophic support for dopaminergic neurons and differentiate into neurons in vitro; implications for tissue engineering and repair in the nervous system", Eur J Neurosci, 19, pp.2388~2398 (2004)
- Arthur A, "Implanted adult human dental pulp stem cells induce endogenous axon guidance", Stem Cells, 27, pp.2229~2237 (2009)
