By contrast, the R206H ACVR1 mutant only slightly enhances the expression of initial and early chondrogenesis markers (collagen type II and aggrecan), consistent with a milder stimulatory effect of the FOP ACVR1 mutation
on chondrocyte differentiation.
Additional tests in tissue samples from osteoarthritic patients who had joint replacements at NYU Langone found similarly increased levels of adenosine A2A receptors
on chondrocytes.
Not exact matches
For instance, to make a rod with collagen fibers aligned along its length (like a tendon) they cultured
chondrocyte cells in a dog bone - shaped mold with loops
on either end.
The findings suggest that reductions in the number of cartilage - producing cells, and greater risk for osteoarthritis, may be driven not just by lower adenosine levels but also by lower levels of the protein
on the surface of
chondrocytes designed to receive and pass
on adenosine's signal.
The study is the first, say its authors, to provide evidence that adenosine, a biochemical at the heart of human cellular function, plays another crucial role — keeping
on hand a steady number of healthy
chondrocytes, the cells that make and sustain cartilage.
This could let synthetic biologists generate tissues
on demand, such as insulin - producing β cells, or cartilage - producing
chondrocytes.
Cronstein and his team also found that levels of adenosine A2A receptors went up
on rat
chondrocytes when osteoarthritis was present, in what the researchers say was a «failed attempt» to compensate for the loss of adenosine from the energy - processing (metabolic) changes underlying the inflammation.
Special focus is placed
on Rho - kinase inhibition, relating to its potential to promote and support extracellular matrix production in cultured
chondrocytes and its role in fibroblast cells as a part of direct chemical cellular differentiation.
Effects of microRNA - 146a
on the proliferation and apoptosis of human osteoarthritis
chondrocytes by targeting TRAF6 through the NF -?
Long - term effects of hydrogel properties
on human
chondrocyte behavior.
Effect of preculture and loading
on expression of matrix molecules, matrix metalloproteinases, and cytokines by expanded osteoarthritic
chondrocytes.
Effects of oxygen
on human
chondrocyte zonal phenotype.
In the meantime, Baojin Yao, postdoctoral fellow, focused
on identifying mechanisms controlling the expression of the SOX9 gene in
chondrocytes (Yao et al., Nucleic Acids Res., 2015).
Based
on previous protocols [5, 6] they have now created a 3D protocol for chondrogenic lineage differentiation via the generation of a putative chondrogenic progenitor cell population, and have found that using this protocol C - iPSCs can be readily differentiated into cartilage in a manner comparable to that of mature
chondrocytes [7].