Functional Analysis of PTH1R Variants Found in Primary Failure of Eruption

First Published January 27, 2020 Research Article Find in PubMed

Authors

12
 
Department of Biochemistry, School of Dentistry, Showa University, Tokyo, Japan
 
Department of Orthodontics, School of Dentistry, Showa University, Tokyo, Japan
by this author
, 1
 
Department of Biochemistry, School of Dentistry, Showa University, Tokyo, Japan
by this author
, 1
 
Department of Biochemistry, School of Dentistry, Showa University, Tokyo, Japan
by this author
,
1
 
Department of Biochemistry, School of Dentistry, Showa University, Tokyo, Japan
by this author
, 34
 
Stem Cell Bank & Division of Stem Cell Processing, Center for Stem Cell Biology and Regenerative Medicine, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan
 
Present address: Department of Transfusion and Cell Transplantation, School of Medicine, Kitasato University, Sagamihara, Japan
by this author
, 5
 
Division of Tissue Engineering, Department of Bone and Cartilage Regenerative Medicine, University of Tokyo Hospital, The University of Tokyo, Tokyo, Japan
by this author
, 2
 
Department of Orthodontics, School of Dentistry, Showa University, Tokyo, Japan
by this author
, 6
 
Laboratory for Gene Regulation, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan
by this author
, 7
 
TOKIWA-Bio, Inc., Tsukuba, Japan
by this author
, 8
 
Biotechnology Research Institute for Drug Discovery, National Institute of Advanced Industrial Science and Technology, Tsukuba, Japan
by this author
, 1
 
Department of Biochemistry, School of Dentistry, Showa University, Tokyo, Japan
by this author
, 1
 
Department of Biochemistry, School of Dentistry, Showa University, Tokyo, Japan
by this author
, 19
 
Department of Biochemistry, School of Dentistry, Showa University, Tokyo, Japan
 
Department of Oral and Maxillofacial Surgery, School of Dentistry, Showa University, Tokyo, Japan
by this author
, 1
 
Department of Biochemistry, School of Dentistry, Showa University, Tokyo, Japan
by this author
, 9
 
Department of Oral and Maxillofacial Surgery, School of Dentistry, Showa University, Tokyo, Japan
by this author
, 2
 
Department of Orthodontics, School of Dentistry, Showa University, Tokyo, Japan
by this author
, 1
 
Department of Biochemistry, School of Dentistry, Showa University, Tokyo, Japan
by this author
...
First Published Online: January 27, 2020

Although many variants of the parathyroid hormone 1 receptor (PTH1R) gene are known to be associated with primary failure of eruption (PFE), the mechanisms underlying the link remains poorly understood. We here performed functional analyses of PTH1R variants reported in PFE patients—namely, 356C>T (P119L), 395C>T (P132L), 439C>T (R147C), and 1148G>A (R383Q)—using HeLa cells with a lentiviral vector-mediated genetic modification. Two particular variants, P119L and P132L, had severe reduction in a level of N-linked glycosylation when compared with wild-type PTH1R, whereas the other 2 showed modest alteration. PTH1R having P119L or P132L showed marked decrease in the affinity to PTH1-34, which likely led to severely impaired cAMP accumulation upon stimulation in cells expressing these mutants, highlighting the importance of these 2 amino acid residues for ligand-mediated proper functioning of PTH1R. To further gain insights into PTH1R functions, we established the induced pluripotent stem cell (iPSC) lines from a patient with PFE and the heterozygous P132L mutation. When differentiated into osteoblastic-lineage cells, PFE-iPSCs showed no abnormality in mineralization. The mRNA expression of RUNX2, SP7, and BGLAP, the osteoblastic differentiation-related genes, and that of PTH1R were augmented in both PFE-iPSC-derived cells and control iPSC-derived cells in the presence of bone morphogenetic protein 2. Also, active vitamin D3 induced the expression of RANKL, a major key factor for osteoclastogenesis, equally in osteoblastic cells derived from control and PFE-iPSCs. In sharp contrast, exposure to PTH1-34 resulted in no induction of RANKL mRNA expression in the cells expressing P132L variant PTH1R, consistent with the idea that a type of heterozygous PTH1R gene mutation would spoil PTH-dependent response in osteoblasts. Collectively, this study demonstrates a link between PFE-associated genetic alteration and causative functional impairment of PTH1R, as well as a utility of iPSC-based disease modeling for future elucidation of pathogenesis in genetic disorders, including PFE.

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