Decreased osteogenic activity and mineralization of alveolar bone cells from a patient with amelogenesis imperfecta and FAM83H 1261G>T mutation

FAM83H mutations lead to autosomal dominant hypocalcified amelogenesis imperfecta (ADHCAI). However, the biological role of FAM83H remains unclear. The present study aimed to characterize the alveolar bone cells isolated from a patient with ADHCAI having the mutation, c.1261G > T, p.E421*, in FAM...

Full description

Bibliographic Details
Main Authors: Nunthawan Nowwarote, Thanaphum Osathanon, Kiattipan Kanjana, Thanakorn Theerapanon, Thantrira Porntaveetus, Vorasuk Shotelersuk
Format: Article
Language:English
Published: Elsevier 2019-12-01
Series:Genes and Diseases
Online Access:http://www.sciencedirect.com/science/article/pii/S2352304219300492
id doaj-310402614e674e30a3d905abe936d870
record_format Article
spelling doaj-310402614e674e30a3d905abe936d8702020-11-25T01:24:53ZengElsevierGenes and Diseases2352-30422019-12-0164391397Decreased osteogenic activity and mineralization of alveolar bone cells from a patient with amelogenesis imperfecta and FAM83H 1261G>T mutationNunthawan Nowwarote0Thanaphum Osathanon1Kiattipan Kanjana2Thanakorn Theerapanon3Thantrira Porntaveetus4Vorasuk Shotelersuk5Genomics and Precision Dentistry Research Unit, Department of Physiology, Faculty of Dentistry, Chulalongkorn University, Bangkok, 10330, ThailandCenter of Excellence for Regenerative Dentistry, Department of Anatomy, Faculty of Dentistry, Chulalongkorn University, Bangkok, 10330, ThailandCenter of Excellence for Regenerative Dentistry, Department of Anatomy, Faculty of Dentistry, Chulalongkorn University, Bangkok, 10330, ThailandGenomics and Precision Dentistry Research Unit, Department of Physiology, Faculty of Dentistry, Chulalongkorn University, Bangkok, 10330, ThailandGenomics and Precision Dentistry Research Unit, Department of Physiology, Faculty of Dentistry, Chulalongkorn University, Bangkok, 10330, Thailand; Corresponding author. Genomics and Precision Dentistry Research Unit, Faculty of Dentistry, Department of Physiology, Faculty of Dentistry, Chulalongkorn University, Bangkok 10330, Thailand. Fax: +662 218 8691.Center of Excellence for Medical Genomics, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, 10330, Thailand; Excellence Center for Medical Genetics, King Chulalongkorn Memorial Hospital, The Thai Red Cross Society, Bangkok, 10330, ThailandFAM83H mutations lead to autosomal dominant hypocalcified amelogenesis imperfecta (ADHCAI). However, the biological role of FAM83H remains unclear. The present study aimed to characterize the alveolar bone cells isolated from a patient with ADHCAI having the mutation, c.1261G > T, p.E421*, in FAM83H. We showed that FAM83H mutant cells had proliferation ability and morphology similar to the controls. The F-actin staining revealed that FAM83H mutant cells were remained in the earlier stages of cell spreading compared to the controls at 30 min, but their spreading was advanced comparable to the controls at later stages. After osteogenic induction, a significant decrease in mRNA levels of RUNX2 and ALP was observed in FAM83H mutant cells at day 7 compared with day 3 while their expressions were increased in the controls. The OPN levels in FAM83H mutant cells were not significantly changed at day 7 compared to day 3 while the controls showed a significant increase. After 14 days, the mineral deposition of FAM83H mutant cells was slightly lower than that of the controls. In conclusion, we identify that FAM83H bone cells have lower expression of osteogenic marker genes and mineralization while they maintain their morphology, proliferation, and spreading. Consistent with previous studies in the ameloblasts and periodontal ligamental cells, these evidences propose that FAM83H influences osteogenic differentiation across different cell types in oral cavity. Keywords: Autosomal dominant inheritance, Enamel hypoplasia, Hypocalcified enamel, Mineralization, Osteogenic differentiation, Periodontiumhttp://www.sciencedirect.com/science/article/pii/S2352304219300492
collection DOAJ
language English
format Article
sources DOAJ
author Nunthawan Nowwarote
Thanaphum Osathanon
Kiattipan Kanjana
Thanakorn Theerapanon
Thantrira Porntaveetus
Vorasuk Shotelersuk
spellingShingle Nunthawan Nowwarote
Thanaphum Osathanon
Kiattipan Kanjana
Thanakorn Theerapanon
Thantrira Porntaveetus
Vorasuk Shotelersuk
Decreased osteogenic activity and mineralization of alveolar bone cells from a patient with amelogenesis imperfecta and FAM83H 1261G>T mutation
Genes and Diseases
author_facet Nunthawan Nowwarote
Thanaphum Osathanon
Kiattipan Kanjana
Thanakorn Theerapanon
Thantrira Porntaveetus
Vorasuk Shotelersuk
author_sort Nunthawan Nowwarote
title Decreased osteogenic activity and mineralization of alveolar bone cells from a patient with amelogenesis imperfecta and FAM83H 1261G>T mutation
title_short Decreased osteogenic activity and mineralization of alveolar bone cells from a patient with amelogenesis imperfecta and FAM83H 1261G>T mutation
title_full Decreased osteogenic activity and mineralization of alveolar bone cells from a patient with amelogenesis imperfecta and FAM83H 1261G>T mutation
title_fullStr Decreased osteogenic activity and mineralization of alveolar bone cells from a patient with amelogenesis imperfecta and FAM83H 1261G>T mutation
title_full_unstemmed Decreased osteogenic activity and mineralization of alveolar bone cells from a patient with amelogenesis imperfecta and FAM83H 1261G>T mutation
title_sort decreased osteogenic activity and mineralization of alveolar bone cells from a patient with amelogenesis imperfecta and fam83h 1261g>t mutation
publisher Elsevier
series Genes and Diseases
issn 2352-3042
publishDate 2019-12-01
description FAM83H mutations lead to autosomal dominant hypocalcified amelogenesis imperfecta (ADHCAI). However, the biological role of FAM83H remains unclear. The present study aimed to characterize the alveolar bone cells isolated from a patient with ADHCAI having the mutation, c.1261G > T, p.E421*, in FAM83H. We showed that FAM83H mutant cells had proliferation ability and morphology similar to the controls. The F-actin staining revealed that FAM83H mutant cells were remained in the earlier stages of cell spreading compared to the controls at 30 min, but their spreading was advanced comparable to the controls at later stages. After osteogenic induction, a significant decrease in mRNA levels of RUNX2 and ALP was observed in FAM83H mutant cells at day 7 compared with day 3 while their expressions were increased in the controls. The OPN levels in FAM83H mutant cells were not significantly changed at day 7 compared to day 3 while the controls showed a significant increase. After 14 days, the mineral deposition of FAM83H mutant cells was slightly lower than that of the controls. In conclusion, we identify that FAM83H bone cells have lower expression of osteogenic marker genes and mineralization while they maintain their morphology, proliferation, and spreading. Consistent with previous studies in the ameloblasts and periodontal ligamental cells, these evidences propose that FAM83H influences osteogenic differentiation across different cell types in oral cavity. Keywords: Autosomal dominant inheritance, Enamel hypoplasia, Hypocalcified enamel, Mineralization, Osteogenic differentiation, Periodontium
url http://www.sciencedirect.com/science/article/pii/S2352304219300492
work_keys_str_mv AT nunthawannowwarote decreasedosteogenicactivityandmineralizationofalveolarbonecellsfromapatientwithamelogenesisimperfectaandfam83h1261gtmutation
AT thanaphumosathanon decreasedosteogenicactivityandmineralizationofalveolarbonecellsfromapatientwithamelogenesisimperfectaandfam83h1261gtmutation
AT kiattipankanjana decreasedosteogenicactivityandmineralizationofalveolarbonecellsfromapatientwithamelogenesisimperfectaandfam83h1261gtmutation
AT thanakorntheerapanon decreasedosteogenicactivityandmineralizationofalveolarbonecellsfromapatientwithamelogenesisimperfectaandfam83h1261gtmutation
AT thantriraporntaveetus decreasedosteogenicactivityandmineralizationofalveolarbonecellsfromapatientwithamelogenesisimperfectaandfam83h1261gtmutation
AT vorasukshotelersuk decreasedosteogenicactivityandmineralizationofalveolarbonecellsfromapatientwithamelogenesisimperfectaandfam83h1261gtmutation
_version_ 1725116518974357504