Deletion of Orai1 leads to bone loss aggravated with aging and impairs function of osteoblast lineage cells

Hyewon Choi, Sonal Srikanth, Elisa Atti, Flavia Q. Pirih, Jeanne Nervina, Yousang Gwack, Sotirios Tetradis

Research output: Contribution to journalArticle

Abstract

Osteoblast lineage cells, a group of cells including mesenchymal progenitors, osteoblasts, and osteocytes, are tightly controlled for differentiation, proliferation and stage-specific functions in processes of skeletal development, growth and maintenance. Recently, the plasma membrane calcium channel Orai1 was highlighted for its role in skeletal development and osteoblast differentiation. Yet the roles of Orai1 in osteoblast lineage cells at various stages of maturation have not been investigated. Herein we report the severe bone loss that occurred in Orai1−/− mice, aggravated by aging, as shown by the microcomputed tomography (mCT) and bone histomorphometry analysis of 8-week and 12-week old Orai1−/− mice and sex-matched WT littermates. We also report that Orai1 deficiency affected the differentiation, proliferation, and type I collagen secretion of primary calvarial osteoblasts, mesenchymal progenitors, and osteocytes in Orai1−/− mice; specifically, our study revealed a significant decrease in the expression of osteocytic genes Fgf23, DMP1 and Phex in the cortical long bone of Orai1−/− mice; a defective cellular and nuclear morphology of Orai1−/− osteocytes; and defective osteogenic differentiation of Orai1−/− primary calvarial osteoblasts (pOBs), including a decrease in extracellular-secretion of type I collagen. An increase in the mesenchymal progenitor population of Orai1−/− bone marrow cells was indicated by a colony forming unit-fibroblasts (CFU-F) assay, and the increased proliferation of Orai1−/− pOBs was indicated by an MTT assay. Notably, Orai1 deficiency reduced the nuclear localization and transcription activity of the Nuclear Factor of Activated T-cell c1 (NFATc1), a calcium-regulated transcription factor, in pOBs. Altogether, our study demonstrated the crucial role of Orai1 in bone development and maintenance, via its diverse effects on osteoblast lineage cells from mesenchymal progenitors to osteocytes.

Original languageEnglish (US)
Pages (from-to)147-155
Number of pages9
JournalBone Reports
Volume8
DOIs
StatePublished - Jun 1 2018

Fingerprint

Osteoblasts
Bone and Bones
Osteocytes
Collagen Type I
Mesenchymal Stromal Cells
Maintenance
Colony-Forming Units Assay
NFATC Transcription Factors
X-Ray Microtomography
Bone Development
Calcium Channels
Ion Channels
Growth and Development
Bone Marrow Cells
Transcription Factors
Fibroblasts
Cell Membrane
Calcium
Gene Expression
Population

Keywords

  • Bone
  • Knockout mice
  • Orai1
  • Osteoblast lineage cells

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Orthopedics and Sports Medicine

Cite this

Choi, H., Srikanth, S., Atti, E., Pirih, F. Q., Nervina, J., Gwack, Y., & Tetradis, S. (2018). Deletion of Orai1 leads to bone loss aggravated with aging and impairs function of osteoblast lineage cells. Bone Reports, 8, 147-155. https://doi.org/10.1016/j.bonr.2018.03.007

Deletion of Orai1 leads to bone loss aggravated with aging and impairs function of osteoblast lineage cells. / Choi, Hyewon; Srikanth, Sonal; Atti, Elisa; Pirih, Flavia Q.; Nervina, Jeanne; Gwack, Yousang; Tetradis, Sotirios.

In: Bone Reports, Vol. 8, 01.06.2018, p. 147-155.

Research output: Contribution to journalArticle

Choi, H, Srikanth, S, Atti, E, Pirih, FQ, Nervina, J, Gwack, Y & Tetradis, S 2018, 'Deletion of Orai1 leads to bone loss aggravated with aging and impairs function of osteoblast lineage cells', Bone Reports, vol. 8, pp. 147-155. https://doi.org/10.1016/j.bonr.2018.03.007
Choi, Hyewon ; Srikanth, Sonal ; Atti, Elisa ; Pirih, Flavia Q. ; Nervina, Jeanne ; Gwack, Yousang ; Tetradis, Sotirios. / Deletion of Orai1 leads to bone loss aggravated with aging and impairs function of osteoblast lineage cells. In: Bone Reports. 2018 ; Vol. 8. pp. 147-155.
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