Title of article
LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye Development
Author/Authors
Yaoqin Gong، نويسنده , , Roger B. Slee، نويسنده , , Naomi Fukai، نويسنده , , Georges Rawadi، نويسنده , , Sergio Roman-Roman، نويسنده , , Anthony M. Reginato، نويسنده , , Hongwei Wang، نويسنده , , Tim Cundy، نويسنده , , Francis H. Glorieux، نويسنده , , Dorit Lev، نويسنده , , Margaret Zacharin، نويسنده , , Konrad Oexle، نويسنده , , Jose Marcelino Oliveira Cavalheiro، نويسنده , , Wafaa Suwairi، نويسنده , , Shauna Heeger، نويسنده , , George Sabatakos، نويسنده , , Suneel Apte، نويسنده , , William N. Adkins، نويسنده , , Jeremy Allgrove، نويسنده , , Mine Arslan-Kirchner، نويسنده , , et al.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2001
Pages
11
From page
513
To page
523
Abstract
In humans, low peak bone mass is a significant risk factor for osteoporosis. We report that LRP5, encoding the low-density lipoprotein receptor-related protein 5, affects bone mass accrual during growth. Mutations in LRP5 cause the autosomal recessive disorder osteoporosis-pseudoglioma syndrome (OPPG). We find that OPPG carriers have reduced bone mass when compared to age- and gender-matched controls. We demonstrate LRP5 expression by osteoblasts in situ and show that LRP5 can transduce Wnt signaling in vitro via the canonical pathway. We further show that a mutant-secreted form of LRP5 can reduce bone thickness in mouse calvarial explant cultures. These data indicate that Wnt-mediated signaling via LRP5 affects bone accrual during growth and is important for the establishment of peak bone mass.
Journal title
CELL
Serial Year
2001
Journal title
CELL
Record number
1017588
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