Cultivo de células epiteliales dentales: impacto del suero fetal bovino

Autores:: Simancas-Escorcia, Victor Hugo
Martinez-Martinez, Adel
Díaz-Caballero, Antonio

Tipo de recurso:: Article of journal

Fecha de publicación:: 2020

Institución:: Universidad de Córdoba

Repositorio:: Repositorio Institucional Unicórdoba

Idioma:: spa

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dc.title.spa.fl_str_mv	Cultivo de células epiteliales dentales: impacto del suero fetal bovino
dc.title.translated.eng.fl_str_mv	Culture of dental epithelial cells: impact of fetal bovine serum
title	Cultivo de células epiteliales dentales: impacto del suero fetal bovino
spellingShingle	Cultivo de células epiteliales dentales: impacto del suero fetal bovino dental enamel ameloblasts culture media serum-free actin mitochondria lysosomes Esmalte dental ameloblastos medio de cultivo libre de suero actina mitocondrias lisosomas
title_short	Cultivo de células epiteliales dentales: impacto del suero fetal bovino
title_full	Cultivo de células epiteliales dentales: impacto del suero fetal bovino
title_fullStr	Cultivo de células epiteliales dentales: impacto del suero fetal bovino
title_full_unstemmed	Cultivo de células epiteliales dentales: impacto del suero fetal bovino
title_sort	Cultivo de células epiteliales dentales: impacto del suero fetal bovino
dc.creator.fl_str_mv	Simancas-Escorcia, Victor Hugo Martinez-Martinez, Adel Díaz-Caballero, Antonio
dc.contributor.author.spa.fl_str_mv	Simancas-Escorcia, Victor Hugo Martinez-Martinez, Adel Díaz-Caballero, Antonio
dc.subject.eng.fl_str_mv	dental enamel ameloblasts culture media serum-free actin mitochondria lysosomes
topic	dental enamel ameloblasts culture media serum-free actin mitochondria lysosomes Esmalte dental ameloblastos medio de cultivo libre de suero actina mitocondrias lisosomas
dc.subject.spa.fl_str_mv	Esmalte dental ameloblastos medio de cultivo libre de suero actina mitocondrias lisosomas
publishDate	2020
dc.date.accessioned.none.fl_str_mv	2020-04-18 00:00:00 2022-07-01T21:01:12Z
dc.date.available.none.fl_str_mv	2020-04-18 00:00:00 2022-07-01T21:01:12Z
dc.date.issued.none.fl_str_mv	2020-04-18
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dc.type.eng.fl_str_mv	Journal article
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dc.relation.references.spa.fl_str_mv	Yuan Y, Chai Y. Chapter Four - Regulatory mechanisms of jaw bone and tooth development. In: Olsen BR, editor. Vertebrate Skeletal Development. Academic Press; 2019. 133:91–118. https://doi.org/10.1016/bs.ctdb.2018.12.013 Balic A, Thesleff I. Chapter Seven - Tissue Interactions Regulating Tooth Development and Renewal. Curr Top Dev Biol. 2015; 115:157-186. https://doi.org/10.1016/bs.ctdb.2015.07.006 Moradian-Oldak J. Protein-mediated enamel mineralization. Front Biosci (Landmark Ed). 2012; 17:1996–2023. http://dx.doi.org/10.2741/4034 Lacruz RS. Enamel: Molecular identity of its transepithelial ion transport system. Cell Calcium. 2017; 65:1–7. https://doi.org/10.1016/j.ceca.2017.03.006 Warshawsky H, Josephsen K, Thylstrup A, Fejerskov O. The development of enamel structure in rat incisors as compared to the teeth of monkey and man. The Anatomical Record. 1981; 200(4):371–399. https://doi.org/10.1002/ar.1092000402 6. Thesleff I. From understanding tooth development to bioengineering of teeth. European Journal of Oral Sciences. 2018; 126(S1):67–71. https://doi-org.gate2.inist.fr/10.1111/eos.12421 Kawano S, Morotomi T, Toyono T, Nakamura N, Uchida T, Ohishi M, et al. Establishment of dental epithelial cell line (HAT-7) and the cell differentiation dependent on Notch signaling pathway. Connect Tissue Res. 2002; 43(2–3):409–412. https://doi.org/10.1080/03008200290000637 Kawasaki K. The SCPP Gene Family and the Complexity of Hard Tissues in Vertebrates. Cells Tissues Organs. 2011; 194(2–4):108–112. https://doi-org.gate2.inist.fr/10.1159/000324225 Nakamura T, Chiba Y, Naruse M, Saito K, Harada H, Fukumoto S. Globoside accelerates the differentiation of dental epithelial cells into ameloblasts. International Journal Of Oral Science. 2016; 8:205. https://doi.org/10.1038/ijos.2016.35 Matsumoto A, Harada H, Saito M, Taniguchi A. Induction of enamel matrix protein expression in an ameloblast cell line co-cultured with a mesenchymal cell line in vitro. In Vitro Cell Dev Biol Anim. 2011; 47(1):39–44. https://doi.org/10.1007/s11626-010-9362-7 Varga G, DenBesten P, Rácz R, Zsembery Á. Importance of bicarbonate transport in pH control during amelogenesis - need for functional studies. Oral Dis. 2018; 24(6):879–890. https://doi.org/10.1111/odi.12738 Abdel Moniem E, Mahmoud EL-Batran M, Mahmoud Halawa A, Hazem Gomaa D, Nour Eldeen G, Mohamed Aly R. Optimizing a serum-free/xeno-free culture medium for culturing and promoting the proliferation of human dental pulp stem cells. Stem Cell Investig 2019; 6:15. http://dx.doi.org/10.21037/sci.2019.06.05 Burnouf T, Strunk D, Koh MBC, Schallmoser K. Human platelet lysate: Replacing fetal bovine serum as a gold standard for human cell propagation? Biomaterials. 2016; 76:371–387. https://doi.org/10.1016/j.biomaterials.2015.10.065 Valk J van der, Bieback K, Buta C, Cochrane B, Dirks WG, Fu J, et al. Fetal bovine serum (FBS): Past – present – future. 1. ALTEX. 2018; 35(1):99–118. https://doi.org/10.14573/altex.1705101 Rácz R, Földes A, Bori E, Zsembery Á, Harada H, Steward MC, et al. No Change in Bicarbonate Transport but Tight-Junction Formation Is Delayed by Fluoride in a Novel Ameloblast Model. Front Physiol. 2017; 8:940. https://doi.org/10.3389/fphys.2017.00940 Park S-J, Lee H-K, Seo Y-M, Son C, Bae HS, Park J-C. Dentin sialophosphoprotein expression in enamel is regulated by Copine-7, a preameloblast-derived factor. Archives of Oral Biology. 2018; 86:131–137. https://doi.org/10.1016/j.archoralbio.2017.12.004 Baker M. Reproducibility: Respect your cells! Nature. 2016; 537:433–435. https://doi.org/10.1038/537433a Wei Z, Batagov AO, Carter DRF, Krichevsky AM. Fetal Bovine Serum RNA Interferes with the Cell Culture derived Extracellular RNA. Sci Rep. 2016; 6:31175. https://doi.org/10.1038/srep31175 van der Valk J, Mellor D, Brands R, Fischer R, Gruber F, Gstraunthaler G, et al. The humane collection of fetal bovine serum and possibilities for serum-free cell and tissue culture. Toxicol In Vitro. 2004; 18(1):1–12. https://doi.org/10.1016/j.tiv.2003.08.009 Burnouf T, Strunk D, Koh MBC, Schallmoser K. Human platelet lysate: Replacing fetal bovine serum as a gold standard for human cell propagation? Biomaterials. 2016; 76:371–387. https://doi.org/10.1016/j.biomaterials.2015.10.065 Wu M-F, Stachon T, Seitz B, Langenbucher A, Szentmáry N. Effect of human autologous serum and fetal bovine serum on human corneal epithelial cell viability, migration and proliferation in vitro. Int J Ophthalmol. 2017; 10(6):908–913. https://doi.org/10.18240/ijo.2017.06.12 Yue B. Biology of the Extracellular Matrix: An Overview. J Glaucoma. 2014; S20–3. https://doi.org/10.1097/IJG.0000000000000108 Wolfenson H, Lavelin I, Geiger B. Dynamic regulation of the structure and functions of integrin adhesions. Dev Cell. 2013; 24(5):447–458. https://doi.org/10.1016/j.devcel.2013.02.012 Pollard TD. Actin and Actin-Binding Proteins. Cold Spring Harb Perspect Biol. 2016; 8(8):a018226. https://doi.org/10.1101/cshperspect.a018226 Brunner D, Frank J, Appl H, Schöffl H, Pfaller W, Gstraunthaler G. Serum-free cell culture: the serum-free media interactive online database. ALTEX. 2010; 27(1):53–62. https://doi.org/10.14573/altex.2010.1.53 Ritchie C. Protease Inhibitors. Mater Methods. 2013; 3:169. https://doi.org/10.13070/mm.en.3.169 Arora M. Cell Culture Media: A Review. Mater Methods 2013; 3:175. https://doi.org/10.13070/mm.en.3.175 Richter U, Lahtinen T, Marttinen P, Myöhänen M, Greco D, Cannino G, et al. A Mitochondrial Ribosomal and RNA Decay Pathway Blocks Cell Proliferation. Current Biology. 2013; 23(6):535–541. https://doi.org/10.1016/j.cub.2013.02.019
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spelling	Simancas-Escorcia, Victor Hugoe45a714d-7723-4e03-b33e-cba354a0caf1-1Martinez-Martinez, Adel8a791591-961b-4687-9c7c-80180d060756-1Díaz-Caballero, Antoniof8ff4111-b51b-4b62-aa42-f8d639001ea6-12020-04-18 00:00:002022-07-01T21:01:12Z2020-04-18 00:00:002022-07-01T21:01:12Z2020-04-180122-0268https://repositorio.unicordoba.edu.co/handle/ucordoba/601010.21897/rmvz.1639https://doi.org/10.21897/rmvz.16391909-0544application/pdfapplication/pdfaudio/mpegaudio/mpegspaUniversidad de Córdobahttps://creativecommons.org/licenses/by-nc-sa/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2https://revistamvz.unicordoba.edu.co/article/view/e1639dental enamelameloblastsculture media serum-freeactinmitochondrialysosomesEsmalte dentalameloblastosmedio de cultivo libre de sueroactinamitocondriaslisosomasCultivo de células epiteliales dentales: impacto del suero fetal bovinoCulture of dental epithelial cells: impact of fetal bovine serumArtículo de revistaJournal articleinfo:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/publishedVersionTexthttp://purl.org/redcol/resource_type/ARTREFhttp://purl.org/coar/version/c_970fb48d4fbd8a85Yuan Y, Chai Y. Chapter Four - Regulatory mechanisms of jaw bone and tooth development. In: Olsen BR, editor. Vertebrate Skeletal Development. Academic Press; 2019. 133:91–118. https://doi.org/10.1016/bs.ctdb.2018.12.013Balic A, Thesleff I. Chapter Seven - Tissue Interactions Regulating Tooth Development and Renewal. Curr Top Dev Biol. 2015; 115:157-186. https://doi.org/10.1016/bs.ctdb.2015.07.006Moradian-Oldak J. Protein-mediated enamel mineralization. Front Biosci (Landmark Ed). 2012; 17:1996–2023. http://dx.doi.org/10.2741/4034Lacruz RS. Enamel: Molecular identity of its transepithelial ion transport system. Cell Calcium. 2017; 65:1–7. https://doi.org/10.1016/j.ceca.2017.03.006Warshawsky H, Josephsen K, Thylstrup A, Fejerskov O. The development of enamel structure in rat incisors as compared to the teeth of monkey and man. The Anatomical Record. 1981; 200(4):371–399. https://doi.org/10.1002/ar.1092000402 6. Thesleff I. From understanding tooth development to bioengineering of teeth. European Journal of Oral Sciences. 2018; 126(S1):67–71. https://doi-org.gate2.inist.fr/10.1111/eos.12421Kawano S, Morotomi T, Toyono T, Nakamura N, Uchida T, Ohishi M, et al. Establishment of dental epithelial cell line (HAT-7) and the cell differentiation dependent on Notch signaling pathway. Connect Tissue Res. 2002; 43(2–3):409–412. https://doi.org/10.1080/03008200290000637Kawasaki K. The SCPP Gene Family and the Complexity of Hard Tissues in Vertebrates. Cells Tissues Organs. 2011; 194(2–4):108–112. https://doi-org.gate2.inist.fr/10.1159/000324225Nakamura T, Chiba Y, Naruse M, Saito K, Harada H, Fukumoto S. Globoside accelerates the differentiation of dental epithelial cells into ameloblasts. International Journal Of Oral Science. 2016; 8:205. https://doi.org/10.1038/ijos.2016.35Matsumoto A, Harada H, Saito M, Taniguchi A. Induction of enamel matrix protein expression in an ameloblast cell line co-cultured with a mesenchymal cell line in vitro. In Vitro Cell Dev Biol Anim. 2011; 47(1):39–44. https://doi.org/10.1007/s11626-010-9362-7Varga G, DenBesten P, Rácz R, Zsembery Á. Importance of bicarbonate transport in pH control during amelogenesis - need for functional studies. Oral Dis. 2018; 24(6):879–890. https://doi.org/10.1111/odi.12738Abdel Moniem E, Mahmoud EL-Batran M, Mahmoud Halawa A, Hazem Gomaa D, Nour Eldeen G, Mohamed Aly R. Optimizing a serum-free/xeno-free culture medium for culturing and promoting the proliferation of human dental pulp stem cells. Stem Cell Investig 2019; 6:15. http://dx.doi.org/10.21037/sci.2019.06.05Burnouf T, Strunk D, Koh MBC, Schallmoser K. Human platelet lysate: Replacing fetal bovine serum as a gold standard for human cell propagation? Biomaterials. 2016; 76:371–387. https://doi.org/10.1016/j.biomaterials.2015.10.065Valk J van der, Bieback K, Buta C, Cochrane B, Dirks WG, Fu J, et al. Fetal bovine serum (FBS): Past – present – future. 1. ALTEX. 2018; 35(1):99–118. https://doi.org/10.14573/altex.1705101Rácz R, Földes A, Bori E, Zsembery Á, Harada H, Steward MC, et al. No Change in Bicarbonate Transport but Tight-Junction Formation Is Delayed by Fluoride in a Novel Ameloblast Model. Front Physiol. 2017; 8:940. https://doi.org/10.3389/fphys.2017.00940Park S-J, Lee H-K, Seo Y-M, Son C, Bae HS, Park J-C. Dentin sialophosphoprotein expression in enamel is regulated by Copine-7, a preameloblast-derived factor. Archives of Oral Biology. 2018; 86:131–137. https://doi.org/10.1016/j.archoralbio.2017.12.004Baker M. Reproducibility: Respect your cells! Nature. 2016; 537:433–435. https://doi.org/10.1038/537433aWei Z, Batagov AO, Carter DRF, Krichevsky AM. Fetal Bovine Serum RNA Interferes with the Cell Culture derived Extracellular RNA. Sci Rep. 2016; 6:31175. https://doi.org/10.1038/srep31175van der Valk J, Mellor D, Brands R, Fischer R, Gruber F, Gstraunthaler G, et al. The humane collection of fetal bovine serum and possibilities for serum-free cell and tissue culture. Toxicol In Vitro. 2004; 18(1):1–12. https://doi.org/10.1016/j.tiv.2003.08.009Burnouf T, Strunk D, Koh MBC, Schallmoser K. Human platelet lysate: Replacing fetal bovine serum as a gold standard for human cell propagation? Biomaterials. 2016; 76:371–387. https://doi.org/10.1016/j.biomaterials.2015.10.065Wu M-F, Stachon T, Seitz B, Langenbucher A, Szentmáry N. Effect of human autologous serum and fetal bovine serum on human corneal epithelial cell viability, migration and proliferation in vitro. Int J Ophthalmol. 2017; 10(6):908–913. https://doi.org/10.18240/ijo.2017.06.12Yue B. Biology of the Extracellular Matrix: An Overview. J Glaucoma. 2014; S20–3. https://doi.org/10.1097/IJG.0000000000000108Wolfenson H, Lavelin I, Geiger B. Dynamic regulation of the structure and functions of integrin adhesions. Dev Cell. 2013; 24(5):447–458. https://doi.org/10.1016/j.devcel.2013.02.012Pollard TD. Actin and Actin-Binding Proteins. Cold Spring Harb Perspect Biol. 2016; 8(8):a018226. https://doi.org/10.1101/cshperspect.a018226Brunner D, Frank J, Appl H, Schöffl H, Pfaller W, Gstraunthaler G. Serum-free cell culture: the serum-free media interactive online database. ALTEX. 2010; 27(1):53–62. https://doi.org/10.14573/altex.2010.1.53Ritchie C. Protease Inhibitors. Mater Methods. 2013; 3:169. https://doi.org/10.13070/mm.en.3.169Arora M. Cell Culture Media: A Review. Mater Methods 2013; 3:175. https://doi.org/10.13070/mm.en.3.175Richter U, Lahtinen T, Marttinen P, Myöhänen M, Greco D, Cannino G, et al. A Mitochondrial Ribosomal and RNA Decay Pathway Blocks Cell Proliferation. Current Biology. 2013; 23(6):535–541. https://doi.org/10.1016/j.cub.2013.02.019https://revistamvz.unicordoba.edu.co/article/download/e1639/2581https://revistamvz.unicordoba.edu.co/article/download/e1639/2582https://revistamvz.unicordoba.edu.co/article/download/e1639/2583https://revistamvz.unicordoba.edu.co/article/download/e1639/2584Núm. 2 , Año 2020 : Revista MVZ Córdoba Volumen 25(2) Mayo-Agosto 2020e16392e163925Revista MVZ CórdobaPublicationOREORE.xmltext/xml3170https://repositorio.unicordoba.edu.co/bitstreams/a3e4aa3c-5d3f-4297-b4bd-9b3e1b5f0559/downloadcbb7eaa96169e680b56a7c26b5693fedMD51ucordoba/6010oai:repositorio.unicordoba.edu.co:ucordoba/60102023-10-06 00:46:59.119https://creativecommons.org/licenses/by-nc-sa/4.0/metadata.onlyhttps://repositorio.unicordoba.edu.coRepositorio Universidad de Córdobabdigital@metabiblioteca.com

Cultivo de células epiteliales dentales: impacto del suero fetal bovino

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