Correlation Engine 2.0
Clear Search sequence regions


  • antigens (2)
  • blood (1)
  • blood cell (2)
  • bone (9)
  • bone marrow (6)
  • bone marrow cells (1)
  • CD105 (1)
  • CD146 (1)
  • CD4 (1)
  • cellular (1)
  • cfu gm (1)
  • CIZ (3)
  • factor (3)
  • female (1)
  • femur (1)
  • genotypes (1)
  • human (2)
  • KO (4)
  • mice (8)
  • mice knockout (1)
  • nestin (1)
  • Nmp4 (5)
  • nuclear matrix (2)
  • organ size (1)
  • osteoblasts (1)
  • osteocalcin (3)
  • osteoclast (1)
  • osteoporosis (1)
  • profiles (2)
  • serum (1)
  • spleen (1)
  • stem cell (5)
  • t lymphocytes (3)
  • Zfp384 protein (1)
  • Sizes of these terms reflect their relevance to your search.

    Parathyroid hormone (PTH) anabolic osteoporosis therapy is intrinsically limited by unknown mechanisms. We previously showed that disabling the transcription factor Nmp4/CIZ in mice expanded this anabolic window while modestly elevating bone resorption. This enhanced bone formation requires a lag period to materialize. Wild-type (WT) and Nmp4-knockout (KO) mice exhibited equivalent PTH-induced increases in bone at 2 weeks of treatment, but by 7 weeks, the null mice showed more new bone. At 3-week treatment, serum osteocalcin, a bone formation marker, peaked in WT mice, but continued to increase in null mice. To determine if 3 weeks is the time when the addition of new bone diverges and to investigate its cellular basis, we treated 10-week-old null and WT animals with human PTH (1-34) (30 μg/kg/day) or vehicle before analyzing femoral trabecular architecture and bone marrow (BM) and peripheral blood phenotypic cell profiles. PTH-treated Nmp4-KO mice gained over 2-fold more femoral trabecular bone than WT by 3 weeks. There was no difference between genotypes in BM cellularity or profiles of several blood elements. However, the KO mice exhibited a significant elevation in CFU-F cells, CFU-F(Alk)(Phos+) cells (osteoprogenitors), and a higher percentage of CFU-F(Alk)(Phos+) cells/CFU-F cells consistent with an increase in CD45-/CD146+/CD105+/nestin+ mesenchymal stem cell frequency. Null BM exhibited a 2-fold enhancement in CD8+ T cells known to support osteoprogenitor differentiation and a 1.6-fold increase in CFU-GM colonies (osteoclast progenitors). We propose that Nmp4/CIZ limits the PTH anabolic window by restricting the number of BM stem, progenitor, and blood cells that support anabolic bone remodeling.

    Citation

    Yongzheng He, Paul Childress, Mark Hood, Marta Alvarez, Melissa A Kacena, Michael Hanlon, Bryce McKee, Joseph P Bidwell, Feng-Chun Yang. Nmp4/CIZ suppresses the parathyroid hormone anabolic window by restricting mesenchymal stem cell and osteoprogenitor frequency. Stem cells and development. 2013 Feb 01;22(3):492-500

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 22873745

    View Full Text