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Papers In Press, published online ahead of print February 25, 2003
J. Biol. Chem, 10.1074/jbc.M207631200
Submitted on July 29, 2002
Revised on January 28, 2003
Accepted on February 25, 2003

Expression of galectin-3 in skeletal tissues is controlled by Runx2

Michael Stock, Henning Schäfer, Sigmar Stricker, Gerhard Gross, Stefan Mundlos, and Florian Otto

Hematology/Oncology, University of Freiburg Medical Center, Freiburg 79106

Corresponding Author: otto{at}mm11.ukl.uni-freiburg.de

The ß-galatoside specific lectin galectin-3 is expressed in vivo in osteoblasts as well as in epiphyseal cartilage. Here we show that in vitro, galectin-3 expression is upregulated in the preosteoblastic cell line MC3T3-E1 during the matrix maturation stage of the osteoblast developmental sequence. Expression persists into late differentiation stages when the mature osteoblastic phenotype is established. The skeletal expression pattern of galectin-3 overlaps at many sites with that of the transcription factor Runx2. Runx2 is a key regulator of osteoblast development and necessary for chondrocyte differentiation in the growth plate. Both human and mouse galectin-3 promoters contain putative Runx binding sites. The constitutive or inducible forced expression of Runx2 is sufficient for the onset of galectin-3 transcription in the mesenchymal precursor cell line C3H10T1/2. Moreover, Runx2 is able to bind to at least two sites in the galectin-3 promoter region. The crucial role of Runx2 was confirmed in Runx2-deficient mice which are devoid of galectin-3 expression in skeletal cells. The overlapping expression pattern of galectin-3 with the other two members of the Runt family of transcription factors (Runx1 and Runx3) points to a potential regulation of the galectin-3 gene (LGALS3) by these factors in hematopoietic, skin and dorsal root ganglial cells.


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