Evidence map›Paper›PMID 16762607›Full record

ArticleBone2006

Correction of the mineralization defect in hyp mice treated with protease inhibitors CA074 and pepstatin.

Peter S N Rowe, Naoko Matsumoto, Oak D Jo, Remi N J Shih, Jeannine Oconnor, Martine P Roudier, Steve Bain, Shiguang Liu, Jody Harrison, Norimoto Yanagawa

Abstract read
In one paragraph

Article in Bone, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. PHEXGenes · 2022
    Article
  3. Kidney stone formation in a novel murine model of polycystic kidney disease.American journal of physiology. Renal physiology · 2022
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Glucocorticoid dose determines osteocyte cell fate.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2011
    Article
  19. Phosphatonins: new hormones involved in numerous inherited bone disorders.Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases · 2011
    Article
  20. Bone proteins PHEX and DMP1 regulate fibroblastic growth factor Fgf23 expression in osteocytes through a common pathway involving FGF receptor (FGFR) signaling.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2011
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Peter S N RoweDepartment of Internal Medicine, The Kidney Institute and Division of Nephrology, MS 3018, University of Kansas Medical Center, 3901 Rainbow Boulevard, 6020B Wahl Hall East, Kansas City, KS 66160, USA. prowe@kumc.edu <prowe@kumc.edu>
Naoko Matsumoto
Oak D Jo
Remi N J Shih
Jeannine Oconnor
Martine P Roudier
Steve Bain
Shiguang Liu
Jody Harrison
Norimoto Yanagawa
University of California, Los Angeles · USUniversity of Kansas Medical Center · USVA Greater Los Angeles Healthcare System · USThe University of Texas Health Science Center at San Antonio · US

Funding

ZDV &3TC NEVIRAPINE COMBINATION THERAPY IN HIV 1 INFECTED INFANTS &M01RR000865 · NCRR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WASHINGTON, ARNOLD E. · 1985 to 2011
$43.4M
TRAFFICKING OF THE PLASMA MEMBRANE CA2+-ATPASE TO RAFTSP20RR017708 · NCRR · UNIVERSITY OF KANSAS LAWRENCE · PI FISCHER, CHRISTOPHER JAMES · 2002 to 2011
$20.1M
Regulation and Function of FGF23R01AR045955 · NIAMS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI QUARLES, L DARRYL · 1999 to 2016
$4.8M
Mineralization of the matrix in disease and healthR01AR051598 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI ROWE, PETER S · 2004 to 2013
$2.8M
Biomedical Research Core Center on Skin Stem CellsP30AR058886 · NIAMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI BICKERS, DAVID RINSEY · 2009 to 2010
$1.5M
Mineralization and the Role of MatrixphosphoglycoproteinR03DE015900 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI ROWE, PETER S · 2004 to 2005
$146k
NCRR NIH HHS 5P20RR017708-03NCRR NIH HHS M01 RR000865NCRR NIH HHS MO1-RR00865NCRR NIH HHS P20 RR017708NIAMS NIH HHS 2 RO1-AR045955-07NIAMS NIH HHS P30 AR058886NIAMS NIH HHS R01 AR045955NIAMS NIH HHS R01 AR051598NIAMS NIH HHS R0-1 AR51598-01NIAMS NIH HHS R0-1 DK-AR58886NIDCR NIH HHS 1R03DE015900-01NIDCR NIH HHS R03 DE015900
6 · The paper itself

Abstract

Increased expression of several osteoblastic proteases and MEPE (a bone matrix protein) occurs in X-linked hypophosphatemic rickets (hyp). This is associated with an increased release of a protease-resistant MEPE peptide (ASARM peptide), a potent inhibitor of mineralization. Cathepsin B cleaves MEPE releasing ASARM peptide and hyp osteoblast/osteocyte cells hypersecrete cathepsin D, an activator of cathepsin B. Our aims were to determine whether cathepsin inhibitors correct the mineralization defect in vivo and whether hyp-bone ASARM peptide levels are reduced after protease treatment. Normal littermates and hyp mice (n = 6) were injected intraperitoneally once a day for 4 weeks with pepstatin, CAO74 or vehicle. Animals were then sacrificed and bones plus serum removed for comprehensive analysis. All hyp mice groups (treated and untreated) remained hypophosphatemic with serum 1,25 vitamin D3 inappropriately normal. Serum PTH was significantly elevated in all hyp mice groups relative to normal mice (P = 0.0017). Untreated hyp mice had six-fold elevated levels of serum alkaline-phosphatase and two-fold elevated levels of ASARM peptides relative to normal mice (P < 0.001). In contrast, serum alkaline phosphatase and serum ASARM peptides were significantly reduced (normalized) in hyp mice treated with CA074 or pepstatin. Serum FGF23 levels remained high in all hyp animal groups (P < 0.0001). Hyp mice treated with protease inhibitors showed dramatic reductions in unmineralized osteoid (femurs) compared to control hyp mice (Goldner staining). Also, hyp animals treated with protease inhibitors showed marked and significant improvements in growth plate width (42%), osteoid thickness (40%) and cortical area (40%) (P < 0.002). The mineralization apposition rate, bone formation rate and mineralization surface were normalized by protease-treatment. High-resolution pQCT mineral histomorphometry measurements and uCT also confirmed a marked mineralization improvement. Finally, the growth plate and cortical bone of hyp femurs contained a massive accumulation of osteoblast-derived ASARM peptide(s) that was reduced in hyp animals treated with CA074 or pepstatin. This study confirms in vivo administration of cathepsin inhibitors improves bone mineralization in hyp mice. This may be due to a protease inhibitor mediated decrease in proteolytic degradation of the extracellular matrix and a reduced release of ASARM peptides (potent mineralization inhibitors).

Indexed as

AnimalsCalcification, PhysiologicCathepsin BCathepsin DExtracellular Matrix ProteinsFemurFibroblast Growth Factor-23ImmunohistochemistryMaleMiceMice, Inbred C57BLMice, Mutant StrainsModels, BiologicalOsteoblastsPepstatinsProtease InhibitorsCathepsin BCathepsin DExtracellular Matrix ProteinsFgf23 protein, mouseFibroblast Growth Factor-23pepstatinPepstatinsProtease Inhibitors

Identifiers

PMID16762607
PMCPMC3358922
OpenAlexW2051375477

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.