Literature DB >> 28122194

Histochemical Examination on Periodontal Tissues of Klotho-Deficient Mice Fed With Phosphate-Insufficient Diet.

Kumiko Hikone1,2, Tomoka Hasegawa1, Erika Tsuchiya1, Hiromi Hongo1, Muneteru Sasaki3, Tomomaya Yamamoto1, Ai Kudo1, Kimimitsu Oda4, Mai Haraguchi1, Paulo Henrique Luiz de Freitas5, Minqi Li6, Junichiro Iida2, Norio Amizuka1.   

Abstract

To elucidate which of elevated serum concentration of inorganic phosphate (Pi) or disrupted signaling linked to αklotho/fibroblast growth factor 23 (FGF23) is a predominant regulator for senescence-related degeneration seen in αKlotho-deficient mice, we have examined histological alteration of the periodontal tissues in the mandibular interalveolar septum of αKlotho-deficient mice fed with Pi-insufficient diet. We prepared six groups of mice: wild-type, kl/kl, and αKlotho-/- mice with normal diet or low-Pi diet. As a consequence, kl/klnorPi and αKlotho-/-norPi mice showed the same abnormalities in periodontal tissues: intensely stained areas with hematoxylin in the interalveolar septum, dispersed localization of alkaline phosphatase-positive osteoblasts and tartrate-resistant acid phosphatase-reactive osteoclasts, and accumulation of dentin matrix protein 1 in the osteocytic lacunae. Although kl/kllowPi mice improved these histological abnormalities, αKlotho-/- lowPi mice failed to normalize those. Gene expression of αKlotho was shown to be increased in kl/kl lowPi specimens. It seems likely that histological abnormalities of kl/kl mice have been improved by the rescued expression of αKlotho, rather than low concentration of serum Pi. Thus, the histological malformation in periodontal tissues in αKlotho-deficient mice appears to be due to not only increased concentration of Pi but also disrupted αklotho/FGF23 signaling.

Entities:  

Keywords:  DMP-1; osteopontin; periodontal tissue; phosphate; αKlotho-deficient mice

Mesh:

Substances:

Year:  2017        PMID: 28122194      PMCID: PMC5407563          DOI: 10.1369/0022155416689670

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


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2.  Molecular cloning and expression analyses of mouse betaklotho, which encodes a novel Klotho family protein.

Authors:  S Ito; S Kinoshita; N Shiraishi; S Nakagawa; S Sekine; T Fujimori; Y I Nabeshima
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Review 3.  Disease model: human aging.

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Journal:  Mol Cell Endocrinol       Date:  2008-09-06       Impact factor: 4.102

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6.  Histomorphometric study of alveolar bone turnover in orthodontic tooth movement.

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9.  Parathyroid hormone receptor signaling in osteocytes increases the expression of fibroblast growth factor-23 in vitro and in vivo.

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Review 10.  Discovery of alpha-Klotho unveiled new insights into calcium and phosphate homeostasis.

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Journal:  Proc Jpn Acad Ser B Phys Biol Sci       Date:  2009       Impact factor: 3.493

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