Dopamine is involved in reparative dentin formation through odontoblastic differentiation of dental pulp stem cells

[1]  U. Müller-Ladner,et al.  Modulation of Dopamine Receptors on Osteoblasts as a Possible Therapeutic Strategy for Inducing Bone Formation in Arthritis , 2022, Cells.

[2]  Zhirong Wang,et al.  Activation of dopamine receptor D1 promotes osteogenic differentiation and reduces glucocorticoid-induced bone loss by upregulating the ERK1/2 signaling pathway , 2022, Molecular medicine.

[3]  A. Tomokiyo,et al.  Secreted Frizzled-Related Protein 1 Promotes Odontoblastic Differentiation and Reparative Dentin Formation in Dental Pulp Cells , 2021, Cells.

[4]  S. Shi,et al.  CD146 controls the quality of clinical grade mesenchymal stem cells from human dental pulp , 2021, Stem cell research & therapy.

[5]  K. Okura,et al.  Risk Factors for Tooth Loss in Patients with ≥25 Remaining Teeth Undergoing Mid-Long-Term Maintenance: A Retrospective Study , 2021, International journal of environmental research and public health.

[6]  K. Matsuo,et al.  Odontoblast death drives cell-rich zone-derived dental tissue regeneration. , 2021, Bone.

[7]  D. Metzger,et al.  Tyrosine hydroxylase conditional KO mice reveal peripheral tissue-dependent differences in dopamine biosynthetic pathways , 2021, The Journal of biological chemistry.

[8]  P. Bártolo,et al.  Electrospun highly porous poly(L-lactic acid)-dopamine-SiO2 fibrous membrane for bone regeneration. , 2020, Materials science & engineering. C, Materials for biological applications.

[9]  M. Clarke,et al.  Efficacy of direct pulp capping for management of cariously exposed pulps in permanent teeth: A systematic review and meta-analysis. , 2020, International endodontic journal.

[10]  K. Keay,et al.  Dopamine: an immune transmitter , 2020, Neural regeneration research.

[11]  T. Ma,et al.  Dopamine D1 receptor-mediated activation of the ERK signaling pathway is involved in the osteogenic differentiation of bone mesenchymal stem cells , 2020, Stem Cell Research & Therapy.

[12]  C. Kitamura,et al.  Expression and function of dopamine in odontoblasts , 2020, Journal of cellular physiology.

[13]  H. Ohshima,et al.  Immunohistochemistry and gene expression of GLUT1, RUNX2 and MTOR in reparative dentinogenesis. , 2019, Oral diseases.

[14]  Masakatsu Watanabe,et al.  Protein S100-A7 Derived from Digested Dentin Is a Critical Molecule for Dentin Pulp Regeneration , 2019, Cells.

[15]  Y. Oda,et al.  Wnt/β-catenin signaling, which is activated in odontomas, reduces Sema3A expression to regulate odontogenic epithelial cell proliferation and tooth germ development , 2019, Scientific Reports.

[16]  D. Tziafas.  Characterization of Odontoblast‐like Cell Phenotype and Reparative Dentin Formation In Vivo: A Comprehensive Literature Review , 2019, Journal of endodontics.

[17]  D. Kaplan,et al.  Functionalization of Silk Fibroin Electrospun Scaffolds via BMSC Affinity Peptide Grafting through Oxidative Self-Polymerization of Dopamine for Bone Regeneration. , 2019, ACS applied materials & interfaces.

[18]  S. An,et al.  The emerging role of extracellular Ca2+ in osteo/odontogenic differentiation and the involvement of intracellular Ca 2+ signaling: From osteoblastic cells to dental pulp cells and odontoblasts , 2018, Journal of cellular physiology.

[19]  A. Tomokiyo,et al.  Senescence and odontoblastic differentiation of dental pulp cells , 2018, Journal of cellular physiology.

[20]  E. Piva,et al.  Disclosing the physiology of pulp tissue for vital pulp therapy , 2018, International endodontic journal.

[21]  M. Delgado-Rodríguez,et al.  Systematic review and meta-analysis. , 2017, Medicina intensiva.

[22]  T. W. Tsutsui,et al.  CD146 positive human dental pulp stem cells promote regeneration of dentin/pulp-like structures , 2018, Human Cell.

[23]  K. Gorseta,et al.  Thermo-cured glass ionomer cements in restorative dentistry , 2017, Journal of Istanbul University Faculty of Dentistry.

[24]  Dong Joon Lee,et al.  Polydopamine-Laced Biomimetic Material Stimulation of Bone Marrow Derived Mesenchymal Stem Cells to Promote Osteogenic Effects , 2017, Scientific Reports.

[25]  A. Tomokiyo,et al.  Calcium-sensing receptor-ERK signaling promotes odontoblastic differentiation of human dental pulp cells. , 2017, Bone.

[26]  H. Miyaji,et al.  Dose effects of beta-tricalcium phosphate nanoparticles on biocompatibility and bone conductive ability of three-dimensional collagen scaffolds. , 2017, Dental materials journal.

[27]  Masahiro Tanaka,et al.  Number of Non-vital Teeth as Indicator of Tooth Loss during 10-year Maintenance: A Retrospective Study. , 2017, The Bulletin of Tokyo Dental College.

[28]  Yu-ping Peng,et al.  Effect of tyrosine hydroxylase overexpression in lymphocytes on the differentiation and function of T helper cells. , 2016, International journal of molecular medicine.

[29]  T. Okiji,et al.  Odontoblasts: Specialized hard‐tissue‐forming cells in the dentin‐pulp complex , 2016, Congenital anomalies.

[30]  Chao Lu,et al.  Retrospective study , 2016, Medicine.

[31]  H. Miyaji,et al.  Semaphorin 3A Induces Odontoblastic Phenotype in Dental Pulp Stem Cells , 2016, Journal of dental research.

[32]  R. Eberhart,et al.  Current status of direct pulp-capping materials for permanent teeth. , 2016, Dental materials journal.

[33]  M. Levite.  Dopamine and T cells: dopamine receptors and potent effects on T cells, dopamine production in T cells, and abnormalities in the dopaminergic system in T cells in autoimmune, neurological and psychiatric diseases , 2016, Acta physiologica.

[34]  Chenxi Zhu,et al.  Clinical outcome of direct pulp capping with MTA or calcium hydroxide: a systematic review and meta-analysis. , 2015, International journal of clinical and experimental medicine.

[35]  J. Launay,et al.  Essential Roles of Dopamine and Serotonin in Tooth Repair: Functional Interplay Between Odontogenic Stem Cells and Platelets , 2015, Stem cells.

[36]  Dong Joon Lee,et al.  Dopaminergic effects on in vitro osteogenesis , 2015, Bone Research.

[37]  F. de Pablo,et al.  Non-neural tyrosine hydroxylase, via modulation of endocrine pancreatic precursors, is required for normal development of beta cells in the mouse pancreas , 2014, Diabetologia.

[38]  A. Baudry,et al.  Pulp stem cells: implication in reparative dentin formation. , 2014, Journal of endodontics.

[39]  J. Ferracane,et al.  Comparison of CaOH with MTA for Direct Pulp Capping , 2013, Journal of dental research.

[40]  Y. Kanda,et al.  Investigation of the freely available easy-to-use software ‘EZR' for medical statistics , 2012, Bone Marrow Transplantation.

[41]  M. Nakatomi,et al.  Expression patterns of nestin and dentin sialoprotein during dentinogenesis in mice. , 2012, Biomedical research.

[42]  A. I. Valenciano,et al.  Tyrosine hydroxylase is expressed during early heart development and is required for cardiac chamber formation. , 2010, Cardiovascular research.

[43]  E. Nemoto,et al.  Elevated extracellular calcium increases expression of bone morphogenetic protein-2 gene via a calcium channel and ERK pathway in human dental pulp cells. , 2010, Biochemical and biophysical research communications.

[44]  S. Gronthos,et al.  Immunomodulatory properties of human periodontal ligament stem cells , 2009, Journal of cellular physiology.

[45]  T. Fujita,et al.  The effect of extracellular calcium ion on gene expression of bone-related proteins in human pulp cells. , 2003, Journal of endodontics.

[46]  J. B. Matthews,et al.  Trans-dentinal Stimulation of Tertiary Dentinogenesis , 2001, Advances in dental research.

[47]  C. Beyer,et al.  Differentiative Effects of Dopamine on Striatal Neurons Involve Stimulation of the cAMP/PKA Pathway , 1998, Molecular and Cellular Neuroscience.

[48]  R. K. Sübay,et al.  Tunnel defects in dentin bridges: their formation following direct pulp capping. , 1996, Operative dentistry.

[49]  G Sundqvist,et al.  Factors affecting the long-term results of endodontic treatment. , 1990, Journal of endodontics.

[50]  S. Udenfriend,et al.  TYROSINE HYDROXYLASE. THE INITIAL STEP IN NOREPINEPHRINE BIOSYNTHESIS. , 1964, The Journal of biological chemistry.