2014, Número 3
<< Anterior Siguiente >>
Rev Odont Mex 2014; 18 (3)
Marcadores candidatos, estrategias de cultivo y perspectivas de las DPSCs como terapia celular en odontología
Romero S, Córdoba K, Martínez VCA, Gutiérrez QJG, Durán RJY, Munévar NJC
Idioma: Español
Referencias bibliográficas: 41
Paginas: 153-163
Archivo PDF: 244.62 Kb.
RESUMEN
La ingeniería tisular basada en las células troncales de pulpa dental se considera como un enfoque prometedor para la odontología regenerativa, con el objetivo final de reemplazar morfológica y funcionalmente los tejidos periodontales y/o los dientes perdidos a través de la síntesis
in vitro de sustitutos análogos tisulares o, incluso, de un diente humano denominado biodiente. Las células troncales de la pulpa dental representan una colonia de células adultas que tienen la capacidad de autorrenovación y diferenciación en diferentes linajes. El origen exacto de las células troncales de la pulpa dental no ha sido completamente determinado y estas células troncales parecen ser la fuente de los odontoblastos que contribuyen a la formación del complejo dentinopulpar. Recientemente, los logros obtenidos a partir de la investigación de las células troncales nos han permitido contemplar las posibles aplicaciones terapéuticas de las células troncales de la pulpa dental. Algunos estudios han demostrado que las células troncales de la pulpa dental son capaces de producir tejidos dentales
in vivo, incluyendo la dentina, la pulpa dental y las estructuras de la corona. Mientras que otras investigaciones han demostrado que estas células troncales se diferencian
in vitro e
in vivo, por ejemplo, en osteoblastos, neuroblastos, condrocitos, fibroblastos y endotelio. En teoría, un biodiente sintetizado a partir de las células troncales de la pulpa dental debe ser la mejor opción para recuperar la totalidad de la estructura y función de un diente humano. El objetivo de este artículo de revisión es hacer una breve descripción de la localización, origen, aislamiento y marcadores candidatos de células troncales de pulpa dental, para así plantear las perspectivas de aplicación en la clínica odontológica.
REFERENCIAS (EN ESTE ARTÍCULO)
Huang AH, Snyder BR, Cheng PH, Chan AW. Putative dental pulp-derived stem/stromal cells promote proliferation and differentiation of endogenous neural cells in the hippocampus of mice. Troncales Cells. 2008; 26: 2654-2663.
Ikeda E, Yagi K, Kojima M, Yagyuu T, Ohshima A, Sobajima S et al. Multipotent cells from the human third molar: feasibility of cell-based therapy for liver disease. Differentiation. 2008; 76: 495-505.
Shi S, Gronthos S. Perivascular niche of postnatal mesenchymal stem cells in human bone marrow and dental pulp. Journal of Bone and Mineral Research. 2003; 18: 696-704.
Shi S, Robey PG, Gronthos S. Comparison of human dental pulp and bone marrow stromal stem cells by cDNA microarray analysis. Bone. 2001; 29: 532-539.
Chai Y, Jiang X, Ito Y, Bringas P Jr, Han J, Rowitch D et al. Fate of the mammalian cranial neural crest during tooth and mandibular morphogenesis. Development. 2000; 127: 1671-1679.
Clouthier DE, Williams SC, Yanagisawa H, Wieduwilt M, Richardson JA, Yanagisawa M. Signaling pathways crucial for craniofacial development revealed by endothelin-A receptor-deficient mice. Developmental Biology. 2000; 217: 10-24.
Zhang J, Duan X, Zhang H, Deng Z, Zhou Z, Wen N et al. Isolation of neural crest-derived stem cells from ratembryonic mandibular processes. Biology of the Cell. 2006; 98: 567-575.
Yan M, Yu Y, Zhang G, Tang C, Yu J. A journey from dental pulp stem cells to a bio-tooth. Stem Cell Rev. 2011; 7: (1) 161–171.
Friedenstein AJ. Precursor cells of mechanocytes. Int Rev Cytol. 1976; 47: 327-359.
Friedenstein AJ, Chailakhjan RK, Lalykina KS. The development of fibroblast colonies in monolayer cultures of guinea-pig bone marrow and spleen cells. Cell Tissue Kinet. 1970; 3: 393-403.
Friedenstein AJ. Stromal mechanisms of bone marrow: cloning in vitro and retransplantation in vivo. Haematol. Blood Transfus. 1980; 25: 19-29.
Huang GT, Sonoyama W, Chen J, Park SH. In vitro characterization of human dental pulp cells: various isolation methods and culturing environments. Cell Tissue Res. 2006; 324: 225-236.
Wiesmann A, Buhring HJ, Mentrup C, Wiesmann HP. Decreased CD90 expression in human mesenchymal stem cells by applying mechanical stimulation. Head Face Med. 2006; 31: 2-8.
Duff S, Li C, Garland J, Kumar S. CD105 is important for angiogénesis: evidence and potential applications. The FASEB Journal. 2003; 17 (9): 982-992.
Gonçalves R, da Silva C, Cabra J, Zanjani E, Almeida-Porada G. STRO-1+ human universal stromal feeder layer to expand/maintain human bone marrow hematopoietic stem/progenitor cells in a serum-free culture sytroncales. Exp Hematol. 2006; 34: 1353-1359.
Gronthos S, Mankani M, Brahim J, Robey PG, Shi S. Postnatal human dental pulp stem cells (DPSCs) in vitro and in vivo. Proc Natl Acad Sci U S A. 2000; 97 (25): 13625-13630.
Miura M, Gronthos S, Zhao M, Lu B, Fisher LW, Robey PG et al. SHED: stem cells from human exfoliated deciduous teeth. Proc Natl Acad Sci U S A. 2003; 100 (10): 5807-5812.
Yu J, Wang Y, Deng Z, Tang L, Li Y, Shi J et al. Odontogenic capability: bone marrow stromal stem cells versus dental pulp stem cells. Biology of the Cell. 2007; 99: 465-474.
Gronthos S, Brahim J, Li W, Fisher LW, Cherman N, Boyde A et al. Stem cell properties of human dental pulp stem cells. J Dent Res. 2002; 81: 531-535.
Yu JH, Deng ZH, Shi JN, Zhai HH, Nie X, Zhuang H et al. Differentiation of dental pulp stem cells into regular-shaped dentin-pulp complex induced by tooth germ cell conditioned medium. Tissue Engineering. 2006; 12: 3097-3105.
Nakashima M, Mizunuma K, Murakami T, Akamine A. Induction of dental pulp stem cell differentiation into odontoblasts by electroporation-mediated gene delivery of growth/differentiation factor 11 (Gdf11). Gene Therapy. 2002; 9: 814-818.
El-Backly RM, Massoud AG, El-Badry AM, Sherif RA, Marei MK. Regeneration of dentine/pulp-like tissue using a dental pulp stem cell/poly (lactic-co-glycolic) acid scaffold construct in New Zealand white rabbits. Australian Endodontic Journal. 2008; 34: 52-67.
Batouli S, Miura M, Brahim J, Tsutsui TW, Fisher LW, Gronthos S et al. Comparison of stem-cell-mediated osteogenesis and dentinogenesis. J Dent Res. 2013; 82 (12): 976-981.
Duailibi MT, Duailibi SE, Young CS, Bartlett JD, Vacanti JP, Yelick PC. Bioengineered teeth from cultured rat tooth bud cells. J Dent Res. 2004; 83: 523-528.
Nakao K, Morita R, Saji Y, Ishida K, Tomita Y, Ogawa M et al. The development of a bioengineered organ germ method. Nature Methods. 2007; 4: 227-230.
Ikeda E, Morita R, Nakao K, Ishida K, Nakamura T, Takano-Yamamoto T et al. Fully functional bioengineered tooth replacement as an organ replacement therapy. Proc Natl Acad Sci U S A. 2009; 106: 13475-13480.
Yu JH, Jin F, Deng ZH, Li YF, Tang L, Shi JN et al. Epithelial-mesenchymal cell ratios can determine the crown morphogenesis of dental pulp stem cells. Stem Cells and Development. 2008; 17: 475-482.
Yu J, Shi J, Jin Y. Current approaches and challenges in making a bio-tooth. Tissue Eng Part B Rev. 2008; 14: 307-319.
Yan X, Qin H, Qu C, Tuan RS, Shi S, Huang GT. iPS cells reprogrammed from human mesenchymal-like stem/progenitor cells of dental tissue origin. Stem Cells and Development. 2010; 19: 469-480.
Okita K, Ichisaka T, Yamanaka S. Generation of germline-competent induced pluripotent stem cells. Nature. 2007; 448: 313-317.
Takahashi K, Tanabe K, Ohnuki M, Narita M, Ichisaka T, Tomoda K et al. Induction of pluripotent stem cells from adult human fibroblasts by defined factors. Cell. 2007; 131: 861-872.
Yu J, Vodyanik MA, Smuga-Otto K, Antosiewicz-Bourget J, Frane JL, Tian S et al. Induced pluripotent stem cell lines derived from human somatic cells. Science. 2007; 318: 1917-1920.
Nakagawa M, Koyanagi M, Tanabe K, Takahashi K, Ichisaka T, Aoi T et al. Generation of induced pluripotent stem cells without myc from mouse and human fibroblasts. Nat Biotechnol. 2008; 26: 101-106.
Rubio D, García-Castro J, Martín MC, de la Fuente R, Cigudosa JC, Lloyd AC et al. Spontaneous human adult stem cell transformation. Cancer Res. 2005; 65 (8): 3035-3039.
Kanematsu A, Yamamoto S, Ozeki M, Noguchi T, Kanatani I, Ogawa O et al. Collagenous matrices as release carriers of exogenous growth factors. Biomaterials. 2004; 25: 4513-4520. [PubMed: 15046942]
Stiver SI, Tan X, Brown LF, Hedley-Whyte ET, Dvorak HF. VEGF-A angiogenesis induces a stable neovasculature in adult murine brain. J Neuropathol Exp Neurol. 2004; 63: 841-55. [PubMed: 15330339]
Nosrat IV, Smith CA, Mullally P, Olson L, Nosrat CA. 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 stem cells. Eur J Neurosci. 2004; 19: 2388-2398. [PubMed: 15128393]
Kolf C, Cho E, Tuan R. Mesenchymal stromal cells. Biology of adult mesenchymal stem cells: regulation of niche, self-renewal and differentiation. Arthritis Res Ther. 2007; 9: 204.
Huang GTJ, Yamaza T, Shea LD, Djouad F, Kuhn NZ, Tuan RS et al. Stem/progenitor cell–mediated de novo regeneration of dental pulp with newly deposited continuous layer of dentin in an in vivo model. Tissue Engineering Part A. 2010; 16: 605-615. [PubMed: 19737072]
Fan Y, Sun Z, Wang R, Abbott C, Moradian-Oldak J. Enamel inspired nanocomposite fabrication through amelogeninsupramolecular assembly. Biomaterials. 2007; 28: 3034-3042. [PubMed: 17382381]
Yin Y, Yun S, Fang J, Chen H. Chemical regeneration of human tooth enamel under nearphysiological conditions. Chem Commun (Camb). 2009; (39): 5892-5894. [PubMed: 19787132]