Inflammatory cytokines regulate proliferation of cultured human osteoblasts

• Published in: Acta orthopaedica Vol. 68; no. 2; pp. 91 - 96
• Main Authors: Frost, Anders, Jonsson, Kenneth B, Nilsson, Olle, Ljunggren, Östen
• Format: Journal Article
• Language: English
• Published: England Informa UK Ltd 1997
• Subjects: Cell Division; Cells, Cultured; Dinoprostone - biosynthesis; Dose-Response Relationship, Drug; Fluorometry; Fracture Healing; Humans; Interleukin-1 - physiology; Interleukin-6 - physiology; Lymphotoxin-alpha - physiology; Osteoblasts - drug effects; Osteoblasts - physiology; Time Factors; Tumor Necrosis Factor-alpha - physiology
• ISSN: 1745-3674; 0001-6470; 1745-3682
• DOI: 10.3109/17453679709003987

We investigated the effects of various pro-inflammatory cytokines on the proliferation rate of isolated human osteoblastic cells in primary cultures. lnterleukin-1ß (IL-1ß) and tumor necrosis factor-ß (TNF-ß) time- and dose-dependently enhanced the proliferation of human osteoblasts. Both of these cytokines also enhanced endogenous prostaglandin E2 (PGE2) formation. Exogenous PGE2 dose- and time-dependently - stimulated cell proliferation. However, the stimulatory effects of IL-1ß and TNF-ß on osteoblast proliferation were not abolished by indomethacin, indicating a direct effect by these cytokines on the rate of proliferation. TNF-α stimulated proliferation at low doses, while it significantly inhibited proliferation at higher concentrations (at and above 100 pM) and with prolonged incubation times. This biphasic effect was unaffected by indomethacin. lnterleukin-6, finally, did not affect the rate of proliferation. Our findings show that inflammatory cytokines may stimulate or inhibit the proliferation of isolated human osteoblasts, depending on concentration and time.