OBJECTIVE: Physical cues play a crucial role in skeletogenesis and osteochondral regeneration. Although human mesenchymal stem cells (hMSCs) offer considerable therapeutic potential, little is known about the molecular mechanisms that control their differentiation. We hypothesized that mechanical strain might be an inherent stimulus for chondrogenic and/or osteogenic differentiation in undifferentiated hMSCs, where c-Fos (FOS) might play a major role in mechanotransduction. METHOD: hMSCs from 10 donors were intermittently stimulated by cyclic tensile strain (CTS) at 3000 mustrain for a period of 3 days. Differential gene expression of strained and unstrained hMSCs was analysed by real-time RT-PCR for several marker genes, including the transcription factors FOS, RUNX2, SOX9, and others. Additionally, alkaline phosphatase activity (ALP) was determined kinetically. RESULTS: The application of CTS significantly stimulated the expression levels of the early chondrogenic and osteogenic marker genes (SOX9, LUM, DCN; RUNX2, SPARC, SPP1, ALPL); this was accompanied by stimulation of ALP activity (+38%+/-12 standard error of mean, P<0.05). Matrix analysis revealed that the osteo-chondrogenic response followed a coordinated expression pattern, in which FOS was attributed to early osteogenic but not chondrogenic differentiation. CONCLUSION: Undifferentiated hMSCs are highly sensitive to mechanical strain with a transcriptionally controlled osteo-chondrogenic differentiation response in vitro.
OBJECTIVE: Physical cues play a crucial role in skeletogenesis and osteochondral regeneration. Although human mesenchymal stem cells (hMSCs) offer considerable therapeutic potential, little is known about the molecular mechanisms that control their differentiation. We hypothesized that mechanical strain might be an inherent stimulus for chondrogenic and/or osteogenic differentiation in undifferentiated hMSCs, where c-Fos (FOS) might play a major role in mechanotransduction. METHOD: hMSCs from 10 donors were intermittently stimulated by cyclic tensile strain (CTS) at 3000 mustrain for a period of 3 days. Differential gene expression of strained and unstrained hMSCs was analysed by real-time RT-PCR for several marker genes, including the transcription factors FOS, RUNX2, SOX9, and others. Additionally, alkaline phosphatase activity (ALP) was determined kinetically. RESULTS: The application of CTS significantly stimulated the expression levels of the early chondrogenic and osteogenic marker genes (SOX9, LUM, DCN; RUNX2, SPARC, SPP1, ALPL); this was accompanied by stimulation of ALP activity (+38%+/-12 standard error of mean, P<0.05). Matrix analysis revealed that the osteo-chondrogenic response followed a coordinated expression pattern, in which FOS was attributed to early osteogenic but not chondrogenic differentiation. CONCLUSION: Undifferentiated hMSCs are highly sensitive to mechanical strain with a transcriptionally controlled osteo-chondrogenic differentiation response in vitro.
Authors: Siddarth D Subramony; Booth R Dargis; Mario Castillo; Evren U Azeloglu; Michael S Tracey; Amanda Su; Helen H Lu Journal: Biomaterials Date: 2012-12-13 Impact factor: 12.479
Authors: Adisri Charoenpanich; Michelle E Wall; Charles J Tucker; Danica M K Andrews; David S Lalush; Douglas R Dirschl; Elizabeth G Loboa Journal: Tissue Eng Part A Date: 2013-09-19 Impact factor: 3.845
Authors: Chad M Teven; Xing Liu; Ning Hu; Ni Tang; Stephanie H Kim; Enyi Huang; Ke Yang; Mi Li; Jian-Li Gao; Hong Liu; Ryan B Natale; Gaurav Luther; Qing Luo; Linyuan Wang; Richard Rames; Yang Bi; Jinyong Luo; Hue H Luu; Rex C Haydon; Russell R Reid; Tong-Chuan He Journal: Stem Cells Int Date: 2011-07-11 Impact factor: 5.443