Interleukin (IL)-13 and IL-4 inhibit proliferation and stimulate IL-6 formation in human osteoblasts:: Evidence for involvement of receptor subunits IL-13R, IL-13Rα, and IL-4Rα

Interleukin-13 (IL-13) inhibits cell proliferation and stimulates interleukin-6 (IL-6) formation in isolated human osteoblasts (hOBs), Because the related cytokine, interleukin-4 (IL-4), is known to exert effects similar to IL-13 in other tissues, and because IL-4 has been implicated as a regulator of hone metabolism, we compared the effects of IL-13 and IL-4 on cell proliferation, IL-6 synthesis, the expression of osteoblastic phenotypic markers in hOB cultures. Also, the receptor proteins mediating these effects in hOBs have been partly characterized. IL-3 and IL-13 dose-dependently inhibited [H-3]-thymidine incorporation into the DNA of human osteoblasts and stimulated secretion of IL-6 into culture supernatants, IL-13 and IL-4 also increased the mRNA levels of IL-6, as measured by RNAse protection assay. Furthermore, IL-13 and IL-4 dose-dependently enhanced alkaline phosphatase (ALP) activity, but did not affect osteocalcin or collagen type I synthesis, IL-4 was tenfold more potent than IL-13 in inducing both ALP activity and IL-6 secretion, whereas the cytokines were equipotent as inhibitors of cell proliferation. The expression of mRNA for receptor subunits previously implicated in IL-4 and IL-13 signaling was investigated by reverse transcriptase-polymerase chain reaction. IL-13R, IL-13R alpha, and IL-4R alpha mRNA were repeatedly detected in hOBs, whereas mRNA for IL-2R gamma (C) was not detected. Receptor-blocking antibodies to IL-4R alpha inhibited the induction of IL-6 Formation by both IL-4 and IL-13, indicating that both cytokines utilize this receptor subunit in signaling. However, the antibodies did not affect the IL-4/-13-induced inhibition of [H-3]-thymidine incorporation or the stimulation of alkaline phosphatase (ALP), suggesting that IL-4R alpha does not mediate these effects of IL-4/-13 in hOBs, We conclude that the cytokines IL-13 and IL-4, through sharing of receptor components, induce similar effects on hOBs, causing inhibition of cell proliferation, stimulation of IL-6, and enhanced ALP activity. (Bone 28:268-274; 2001) (C) 2001 by Elsevier Science Inc. All rights reserved.