z-logo
Premium
Lymphocyte enhancer‐binding factor 1 (Lef1) inhibits terminal differentiation of osteoblasts
Author(s) -
Kahler Rachel A.,
Galindo Mario,
Lian Jane,
Stein Gary S.,
van Wijnen Andre J.,
Westendorf Jennifer J.
Publication year - 2005
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.20702
Subject(s) - osteoblast , runx2 , osteocalcin , wnt signaling pathway , microbiology and biotechnology , chemistry , downregulation and upregulation , mesenchymal stem cell , cellular differentiation , alkaline phosphatase , biology , signal transduction , gene , biochemistry , in vitro , enzyme
Lef1 is a transcriptional regulator of the Wnt/β‐catenin signaling cascade. Wnts directly augment bone formation and osteoblast differentiation from mesenchymal stem cells by receptor‐mediated pathways involving Lrp5 and Frizzled. We previously reported that Lef1 represses Runx2‐dependent activation of the late osteoblast differentiation gene, osteocalcin. Lef1 is expressed in preosteoblasts but is undetectable in fully differentiated osteoblasts. To determine if downregulation of Lef1 is necessary for osteoblast maturation, we constitutively overexpressed Lef1 in MC3T3‐E1 preosteoblasts. Lef1‐overexpressing cells produced alkaline phosphatase (ALP) and osteocalcin later, and at lower levels than control cells. Moreover, the extracellular matrices of Lef1‐overexpressing cell cultures never mineralized. To further examine the role of Lef1 in osteoblasts, we suppressed Lef1 expression in MC3T3‐E1 cells by RNA interference. Transient expression of a Lef1 shRNA efficiently reduced murine Lef1 levels and transcriptional activity. Stable suppression of Lef1 in MC3T3 preosteoblasts did not affect proliferation or Runx2 levels; however, ALP production and matrix mineralization were accelerated by 3–4 days. Gene chip analyses identified 14 genes that are differentially regulated in Lef1‐suppressed cells. These data outline a role for Lef1 in delaying osteoblast maturation and suggest that Lef1 controls the expression of multiple genes in osteoblasts. J. Cell. Biochem. 97: 969–983, 2006. © 2005 Wiley‐Liss, Inc.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here