TNFα promotes osteogenic differentiation of human mesenchymal stem cells by triggering the NF-κB signaling pathway

• Published in: Bone (New York, N.Y.) Vol. 45; no. 2; pp. 367 - 376
• Main Authors: Hess, Katrin, Ushmorov, Alexey, Fiedler, Jörg, Brenner, Rolf E., Wirth, Thomas
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier Inc 01.08.2009; Elsevier
• Subjects: Biological and medical sciences; Bone morphogenic protein 2 (BMP-2); Cell physiology; Fundamental and applied biological sciences. Psychology; Matrix mineralization; Mesenchymal stem cells; Mineralization, calcification; Molecular and cellular biology; Nuclear factor kappaB (NF-κB); Orthopedics; Osteogenic differentiation; Vertebrates: anatomy and physiology, studies on body, several organs or systems; Matrix mineralization; Osteogenic differentiation; Nuclear factor kappaB (NF-κB); Bone morphogenic protein 2 (BMP-2); Mesenchymal stem cells; Human; Stem cell; Mesenchymal cell; Bone morphogenetic protein-2; Mineralization; Morphology; Transcription factor NFκB; Bone; Tumor necrosis factor α
• DOI: 10.1016/j.bone.2009.04.252
• ISSN: 8756-3282

Mesenchymal stem cells are multipotent cells able to differentiate into different mesenchymal lineages. Studies in the past had suggested that two of these mesenchymal differentiation directions, the chondrogenic and the myogenic differentiation, are negatively regulated by the transcription factor NF-κB. Although osteogenic differentiation has been extensively studied, the influence of NF-κB on this differentiation lineage was not subject of detailed analyses in the past. We have analyzed the consequences of TNF-α treatment and genetic manipulation of the NF-κB pathway for osteogenic differentiation of hMSCs. Treatment of hMSCs during differentiation with TNF-α activates NF-κB and this results in enhanced expression of osteogenetic proteins like bone morphogenetic protein2 (BMP-2) and alkaline phosphatase (ALP). In addition, enhanced matrix mineralization was observed. The direct contribution of the NF-κB pathway was confirmed in cells that express a constitutively active version of the NF-κB-inducing kinase IKK2 (CA-IKK2). The IKK2/NF-κB-induced BMP-2 up-regulation results in the enhancement of RUNX2 and Osterix expression, two critical regulators of the osteogenic differentiation program. Interestingly, a genetic block of the NF-κB pathway did not interfere with osteogenic differentiation. We conclude that TNFα mediated NF-κB activation, although not absolutely required for BMP-2 expression and matrix mineralization nevertheless supports osteogenic differentiation and matrix mineralization by increasing BMP-2 expression. Our results therefore suggest that NF-κB activation may function in lineage selection during differentiation of hMSCs by fostering osteogenic differentiation at the expense of other differentiation lineages.