Wnts differentially regulate colony growth and differentiation of chondrogenic rat calvaria cells

The wingless- and int-related proteins (Wnts) have an important role during embryonic development and limb patterning. To investigate their function d uring chondrocyte differentiation, we used NIH3T3 cells producing seven mem bers of the Wnt family and secreted frizzled-related protein (sFRP-2) for c o-culture experiments with the rat chondrogenic cell line pColl(II)-EGFP-5. Pilot experiments showed a negative effect of Wnt-7a on the proliferation of three rodent chondrogenic cell lines, RCJ3.1(C5.18), CFK-2, and C1. To e stablish a reporter system for chondrogenic differentiation we then produce d a stably transfected chondrogenic cell line based on RCJ3.1(C5.18) for fu rther experiments, which expresses green fluorescence protein (EGFP) under the collagen type II promoter (pColl(II)-EGFP-5). This cell line permits co nvenient observation of green fluorescence as a marker for differentiation in lift cultures. The colony size of this cell line in agarose suspension c ultures was reduced to 20-40% of control, when exposed to Wnt-1, 3a, 4, 7a, and 7b for 14 days. Similarly, reporter gene expression and the synthesis of cartilage-specific proteoglycans were inhibited by this group of Wnts. I n contrast, pColl(II)-EGFP-5 cells exposed to Wnt-5a and Wnt-11 reached 140 % of control, and reporter gene expression and proteoglycan synthesis were stimulated. The effects of Wnt-7a and Wnt-5a were additive in pColl(II)-EGF P-5 cells and some but not all Wnt effects were antagonized by the inhibiti on of proteoglycan sulfation with chlorate, by sFRP-2. which may modulate W nt receptor binding, or by inhibitors of protein kinase C. These results su ggest two functional Wnt subclasses that differentially regulate proliferat ion and chondrogenic differentiation in vitro which may have implications f or cartilage differentiation in vivo. Since some, but not all Wnt effects w ere sensitive to inhibitors of proteoglycan synthesis or protein kinase C, multiple modes of signal transduction may be involved. (C) 2001 Elsevier Sc ience B.V. All rights reserved.