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Biology subjects

Tanner, G. I.

Publications and source records attributed to Tanner, G. I..

2 recordsLinked to original sources

YAP regulates periosteal expansion in fracture repair

Bone fracture repair initiates by periosteal expansion. The periosteum is typically quiescent, but upon fracture, periosteal cells proliferate and contribute to bone fracture repair. The expansion of the periosteum is regulated by gene transcription; however, the molecular mechanisms behind periosteal expansion are unclear. Here, we show that Yes-Associated Protein (YAP) and transcriptional co-activator with PDZ-binding motif (TAZ) mediate periosteal expansion and periosteal cell proliferation. Bone fracture increases the number of YAP-expressing periosteal cells, and deletion of YAP and TAZ from Osterix (Osx) expressing cells impairs early periosteal expansion. Mechanistically, YAP regulates both cell-intrinsic and cell-extrinsic factors that allow for periosteal expansion. Specifically, we identified Bone Morphogenetic Protein 4 (BMP4) as a cell extrinsic factor regulated by YAP, that rescues the impairment of periosteal expansion upon YAP/TAZ deletion. Together, these data establish YAP mediated transcriptional mechanisms that induce periosteal expansion in the early stages of fracture repair and provide new putative targets for therapeutic interventions.

cell biology↗

Granular hydrogels improve myogenic invasion and repair after volumetric muscle loss

Skeletal muscle injuries including volumetric muscle loss (VML) are marked by excessive scarring and functional disability that inherent regenerative mechanisms are unable to reverse. Despite high prevalence in civilian and military populations, there is currently no effective treatment for VML but bioengineering interventions such as biomaterials that fill the VML defect to support tissue growth and repair are a promising strategy. However, traditional biomaterials developed for this purpose are rigid, non-porous constructs that hinder cell infiltration. In the present study, we test the effects of granular hydrogels on muscle repair - hypothesizing that their inherent porosity will support the invasion of native myogenic cells and their flowability will permit conformable filling of the defect site, leading to effective muscle repair. We used photocurable hyaluronic acid crosslinked with matched muscle stiffness to prepare small or large particle fragments via extrusion fragmentation and facile size sorting. In assembled granular hydrogels, particle size and degree of packing significantly influenced pore features including porosity, pore size, and pore density, as well as rheological behavior including storage moduli and yield strain. We tested the ability of granular hydrogels to support early-stage (satellite cell invasion) and late-stage (myofiber invasion) muscle repair compared to bulk hydrogels in a VML injury model in the tibialis anterior (TA) muscles of 12-14 week old mice. Histological evaluation revealed granular hydrogels supported these regenerative processes while control bulk hydrogels restricted them to the gel-tissue interface in line with the absence of invading cells. Together, these results highlight the promising potential of injectable and porous granular hydrogels in supporting endogenous repair after severe muscle injury.

bioengineering↗