Controlling osteogenic stem cell differentiation via soft bioinspired hydrogels

• Published in: PloS one 2014-06, Vol.9 (6), p.e98640-e98640
• Main Authors: Jha, Amit K, Jackson, Wesley M, Healy, Kevin E
• Format: Article
• Language: English
• Subjects: Acrylamides - chemistry; Adhesion tests; Alkaline phosphatase; Alkaline Phosphatase - metabolism; Antigens; Arthritis; Biocompatibility; Biocompatible Materials; Bioengineering; Biology and Life Sciences; Bone growth; Bone marrow; Bone sialoprotein; Cbfa-1 protein; Cell Adhesion; Cell Differentiation; Cell Proliferation; Cells, Cultured; Collagen Type I - metabolism; Core Binding Factor Alpha 1 Subunit - metabolism; Culture Media; Differentiation (biology); Endochondral bone; Extracellular matrix; Gene expression; Humans; Hydrogels; Hydrogels - chemistry; Integrin-Binding Sialoprotein - metabolism; Interpenetrating networks; Intramembraneous bone; Isopropylacrylamide; Laboratories; Ligands; Mesenchymal Stem Cells - physiology; Mesenchyme; Microscopy; Oligopeptides - chemistry; Ossification; Osteoblasts - physiology; Osteocalcin - metabolism; Osteogenesis; Peptides; Physical Sciences; Poly(N-isopropylacrylamide); Skin & tissue grafts; Sodium; Stem cells; Stiffness; Studies; Substrates
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0098640

Osteogenic differentiation of human mesenchymal stem cells (hMSCs) is guided by various physical and biochemical factors. Among these factors, modulus (i.e., rigidiy) of the ECM has gained significant attention as a physical osteoinductive signal that can contribute to endochondral ossification of a cartilaginous skeletal template. However, MSCs also participate in intramembranous bone formation, which occurs de novo from within or on a more compliant tissue environment. To further understand the role of the matrix interactions in this process, we evaluated osteogenic differentiation of hMSCs cultured on low moduli (102, 390 or 970 Pa) poly(N-isopropylacrylamide) (p(NIPAAm)) based semi-interpenetrating networks (sIPN) modified with the integrin engaging peptide bsp-RGD(15) (0, 105 or 210 µM). Cell adhesion, proliferation, and osteogenic differentiation of hMSCs, as measured by alkaline phosphatase (ALP), runt-related transcription factor 2 (RUNX2), bone sialoprotein-2 (iBSP), and osteocalcien (OCN) protein expression, was highest on substrates with the highest modulus and peptide concentrations. However, within this range of substrate stiffness, many osteogenic cellular functions were enhanced by increasing either the modulus or the peptide density. These findings suggest that within a compliant and low modulus substrate, a high affinity adhesive ligand serves as a substitute for a rigid matrix to foster osteogenic differentiation.