Effect of high phosphate diet on the formation of dentin in Fam20c‐deficient mice

FAM20C (family with sequence similarity 20‐member C), a kinase that phosphorylates secretory proteins, plays essential roles in various biological processes. In humans, mutations in FAM20C gene cause Raine syndrome, an autosomal recessive hereditary disease manifesting a broad spectrum of developmen...

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Published inEuropean journal of oral sciences Vol. 129; no. 3; pp. e12795 - n/a
Main Authors Zhang, Hua, Xu, Qian, Lu, Yongbo, Qin, Chunlin
Format Journal Article
LanguageEnglish
Published England Wiley Subscription Services, Inc 01.06.2021
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ISSN0909-8836
1600-0722
1600-0722
DOI10.1111/eos.12795

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Abstract FAM20C (family with sequence similarity 20‐member C), a kinase that phosphorylates secretory proteins, plays essential roles in various biological processes. In humans, mutations in FAM20C gene cause Raine syndrome, an autosomal recessive hereditary disease manifesting a broad spectrum of developmental defects including skeletal and craniofacial deformities. Our previous studies revealed that inactivation of Fam20c in mice led to hypophosphatemic rickets and that high phosphate (hPi) diet significantly improved the development of the skeleton in Fam20c‐deficient mice. In this study, we evaluated the effects of hPi diet on the formation of dentin in Fam20c‐deficient mice, using plain x‐ray radiography, micro–computed tomography (µCT), histology, and immunohistochemistry. Plain x‐ray radiography and µCT analyses showed that the hPi diet improved the dentin volume fraction and dentin mineral density of the Fam20c‐deficient mice. Histology analyses further demonstrated that the hPi diet dramatically improved the integrity of the mandibular first molars and prevented pulp infection and dental abscesses in Fam20c‐deficient mice. Our results support that the hPi diet significantly increased the formation and mineralization of dentin in Fam20c‐deficient mice, implying that hypophosphatemia is a significant contributor to the dentin defects in Fam20c‐deficient subjects.
AbstractList FAM20C (family with sequence similarity 20‐member C), a kinase that phosphorylates secretory proteins, plays essential roles in various biological processes. In humans, mutations in FAM20C gene cause Raine syndrome, an autosomal recessive hereditary disease manifesting a broad spectrum of developmental defects including skeletal and craniofacial deformities. Our previous studies revealed that inactivation of Fam20c in mice led to hypophosphatemic rickets and that high phosphate (hPi) diet significantly improved the development of the skeleton in Fam20c‐deficient mice. In this study, we evaluated the effects of hPi diet on the formation of dentin in Fam20c‐deficient mice, using plain x‐ray radiography, micro–computed tomography (µCT), histology, and immunohistochemistry. Plain x‐ray radiography and µCT analyses showed that the hPi diet improved the dentin volume fraction and dentin mineral density of the Fam20c‐deficient mice. Histology analyses further demonstrated that the hPi diet dramatically improved the integrity of the mandibular first molars and prevented pulp infection and dental abscesses in Fam20c‐deficient mice. Our results support that the hPi diet significantly increased the formation and mineralization of dentin in Fam20c‐deficient mice, implying that hypophosphatemia is a significant contributor to the dentin defects in Fam20c‐deficient subjects.
FAM20C (family with sequence similarity 20-member C), a kinase that phosphorylates secretory proteins, plays essential roles in various biological processes. In humans, mutations in FAM20C gene cause Raine syndrome, an autosomal recessive hereditary disease manifesting a broad spectrum of developmental defects including skeletal and craniofacial deformities. Our previous studies revealed that inactivation of Fam20c in mice led to hypophosphatemic rickets and that high phosphate (hPi) diet significantly improved the development of the skeleton in Fam20c-deficient mice. In this study, we evaluated the effects of hPi diet on the formation of dentin in Fam20c-deficient mice, using plain x-ray radiography, micro-computed tomography (µCT), histology, and immunohistochemistry. Plain x-ray radiography and µCT analyses showed that the hPi diet improved the dentin volume fraction and dentin mineral density of the Fam20c-deficient mice. Histology analyses further demonstrated that the hPi diet dramatically improved the integrity of the mandibular first molars and prevented pulp infection and dental abscesses in Fam20c-deficient mice. Our results support that the hPi diet significantly increased the formation and mineralization of dentin in Fam20c-deficient mice, implying that hypophosphatemia is a significant contributor to the dentin defects in Fam20c-deficient subjects.FAM20C (family with sequence similarity 20-member C), a kinase that phosphorylates secretory proteins, plays essential roles in various biological processes. In humans, mutations in FAM20C gene cause Raine syndrome, an autosomal recessive hereditary disease manifesting a broad spectrum of developmental defects including skeletal and craniofacial deformities. Our previous studies revealed that inactivation of Fam20c in mice led to hypophosphatemic rickets and that high phosphate (hPi) diet significantly improved the development of the skeleton in Fam20c-deficient mice. In this study, we evaluated the effects of hPi diet on the formation of dentin in Fam20c-deficient mice, using plain x-ray radiography, micro-computed tomography (µCT), histology, and immunohistochemistry. Plain x-ray radiography and µCT analyses showed that the hPi diet improved the dentin volume fraction and dentin mineral density of the Fam20c-deficient mice. Histology analyses further demonstrated that the hPi diet dramatically improved the integrity of the mandibular first molars and prevented pulp infection and dental abscesses in Fam20c-deficient mice. Our results support that the hPi diet significantly increased the formation and mineralization of dentin in Fam20c-deficient mice, implying that hypophosphatemia is a significant contributor to the dentin defects in Fam20c-deficient subjects.
FAM20C (family with sequence similarity 20-member C), a kinase that phosphorylates secretory proteins, plays essential roles in various biological processes. In humans, mutations in FAM20C gene cause Raine syndrome, an autosomal recessive hereditary disease manifesting a broad spectrum of developmental defects including skeletal and craniofacial deformities. Our previous studies revealed that inactivation of Fam20c in mice led to hypophosphatemic rickets and that high phosphate (hPi) diet significantly improved the development of the skeleton in Fam20c- deficient mice. In this study, we evaluated the effects of hPi diet on the formation of dentin in Fam20c -deficient mice, using plain x-ray radiography, micro–computed tomography (μCT), histology, and immunohistochemistry. Plain x-ray radiography and μCT analyses showed that the hPi diet improved the dentin volume fraction and dentin mineral density of the Fam20c -deficient mice. Histology analyses further demonstrated that the hPi diet dramatically improved the integrity of the mandibular first molars and prevented pulp infection and dental abscesses in Fam20c -deficient mice. Our results support that the hPi diet significantly increased the formation and mineralization of dentin in Fam20c -deficient mice, implying that hypophosphatemia is a significant contributor to the dentin defects in Fam20c -deficient subjects.
Author Zhang, Hua
Xu, Qian
Qin, Chunlin
Lu, Yongbo
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Keywords mouse
FAM20C
dentin
high phosphate diet
hypophosphatemia
Language English
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Notes Funding information
This work was supported by USA National Institute of Health Grant DE022549 (to CQ) and, Texas A&M University College of Dentistry Department of Biomedical Sciences Seed Grant TAMCOD‐BMS‐2019‐004 (to HZ).
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Conceptualization: Hua Zhang, Yongbo Lu, Chunlin Qin; Formal analysis: Hua Zhang, Yongbo Lu; Chunlin Qin; Investigation: Hua Zhang, Qian Xu, Yongbo Lu, Chunlin Qin. Writing- original draft preparation and Writing-review and editing: Hua Zhang, Qian Xu, Yongbo Lu, Chunlin Qin; Supervision and Project administration: Hua Zhang, Chunlin Qin.
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Snippet FAM20C (family with sequence similarity 20‐member C), a kinase that phosphorylates secretory proteins, plays essential roles in various biological processes....
FAM20C (family with sequence similarity 20-member C), a kinase that phosphorylates secretory proteins, plays essential roles in various biological processes....
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SubjectTerms Abscesses
Animals
Biological activity
Calcium-Binding Proteins - genetics
Computed tomography
Defects
Dental pulp
Dentin
Dentin - metabolism
Diet
Extracellular Matrix Proteins - genetics
Extracellular Matrix Proteins - metabolism
FAM20C
Hereditary diseases
high phosphate diet
Histology
Hypophosphatemia
Immunohistochemistry
Inactivation
Kinases
Mice
Mice, Knockout
Mineralization
Molars
mouse
Mutation
Phosphates
Radiography
Rickets
Rodents
Skeleton
X-Ray Microtomography
Title Effect of high phosphate diet on the formation of dentin in Fam20c‐deficient mice
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Feos.12795
https://www.ncbi.nlm.nih.gov/pubmed/33905141
https://www.proquest.com/docview/2531480619
https://www.proquest.com/docview/2518970912
https://pubmed.ncbi.nlm.nih.gov/PMC8183185
Volume 129
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