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Reduced bone mineral density in SOCS-2-deficient mice.

Lorentzon, Mattias, 1970 (author)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin,Institute of Internal Medicine
Greenhalgh, Chris J (author)
Mohan, Subburaman (author)
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Alexander, Warren S (author)
Ohlsson, Claes, 1965 (author)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för internmedicin,Institute of Internal Medicine, Dept of Medicine
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 (creator_code:org_t)
2005
2005
English.
In: Pediatric research. - 0031-3998. ; 57:2, s. 223-6
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Suppressor of cytokine signaling-2 (SOCS-2) is a member of the suppressor of cytokine signaling family, implicated in the negative regulation of cytokine action through inhibition of the Janus kinase (JAK) signal transducers and activators of transcription (STAT) signal transduction pathway. We have previously reported that SOCS-2-/- mice display an increased longitudinal skeletal growth associated with a deregulated GH/IGF-I signaling. The aim of the present study was to determine the role of SOCS-2 in the regulation of bone mineral density (BMD). Dual x-ray absorptiometry (DXA) analyses demonstrated that the areal BMD of the tibia was reduced in both 4-wk-old (-8.6%) and 15-wk-old (-6.0%) SOCS 2-/- mice compared with wild-type (WT) mice. The trabecular volumetric BMD, as measured by peripheral quantitative computerized tomography (pQCT) in the metaphyseal region of the distal femur, was reduced in both 4-wk-old (-10%) and 15-wk-old (-32%) SOCS 2-/- mice compared with WT mice. pQCT analyses in the diaphyseal region of tibia also revealed that the cortical volumetric BMD was reduced in both 4-wk-old (-7%) and 15-wk-old (-3%) SOCS 2-/- mice. The cortical cross-sectional area was reduced in 4-wk-old but not in 15-wk-old SOCS 2-/- mice. In conclusion, SOCS-2 inactivation results in reduced trabecular and cortical volumetric BMD. These effects are not consistent with an augmented GH/IGF-I signaling and, therefore, the mechanism behind the reduced BMD remains to be elucidated.

Keyword

Animals
Bone Density
Bone and Bones
metabolism
DNA-Binding Proteins
genetics
physiology
Femur
metabolism
Insulin-Like Growth Factor I
metabolism
Janus Kinase 1
Male
Mice
Mice
Inbred C57BL
Mice
Transgenic
Osteocalcin
metabolism
Protein-Tyrosine Kinases
metabolism
Repressor Proteins
genetics
physiology
Signal Transduction
Suppressor of Cytokine Signaling Proteins
Time Factors
Tomography
X-Ray Computed
Trans-Activators
genetics
physiology

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