| Autor: |
Birks S; Boise State University, Micron School of Materials Science and Engineering., Howard S; Boise State University, Mechanical and Biomedical Engineering., Wright CS; Indiana University, Department of Physical Therapy, School of Health and Human Sciences., O'Rourke C; The College of New Jersey, Biomedical Engineering., Day EA; Indiana University, Department of Physical Therapy, School of Health and Human Sciences., Lamb AJ; Indiana University, Department of Physical Therapy, School of Health and Human Sciences., Walsdorf JR; Indiana University, Department of Physical Therapy, School of Health and Human Sciences., Lau A; The College of New Jersey, Biomedical Engineering., Thompson WR; Indiana University, Department of Physical Therapy, School of Health and Human Sciences., Uzer G; Boise State University, Mechanical and Biomedical Engineering. |
| Abstrakt: |
The Linker of Nucleoskeleton and Cytoskeleton (LINC) complex serves to connect the nuclear envelope and the cytoskeleton, influencing cellular processes such as nuclear arrangement, architecture, and mechanotransduction. The role LINC plays in mechanotransduction pathways in bone progenitor cells has been well studied; however, the mechanisms by which LINC complexes govern in vivo bone formation remain less clear. To bridge this knowledge gap, we established a murine model disrupting LINC using transgenic Prx-Cre mice and floxed Tg(CAG-LacZ/EGFP-KASH2) mice. Prx-Cre mice express the Cre recombinase enzyme controlled by the paired-related homeobox gene-1 promoter ( Prrx1 ), a pivotal regulator of skeletal development. Prx-Cre animals have been widely used in the bone field to target bone progenitor cells. Tg(CAG-LacZ/EGFP-KASH2) mice carry a lox-stop-lox flanked LacZ gene allowing for the overexpression of an EGFP-KASH2 fusion protein via cre recombinase mediated deletion of the LacZ cassette. This disrupts endogenous Nesprin-Sun binding in a dominant negative manner disconnecting nesprin from the nuclear envelope. By combining these lines, we generated a Prrx1(+) cell-specific LINC disruption model to study its impact on the developing skeleton and subsequently exercise-induced bone accrual. The findings presented here indicate Prx-driven LINC disruption (PDLD) cells exhibit no change in osteogenic and adipogenic potential compared to controls in vitro nor are there bone quality changes when compared to in sedentary animals at 8 weeks. While PDLD animals displayed increased voluntary running activity andPrrx1(+) cell-specific LINC disruption abolished the exercise-induced increases in osteoid volume and surface after a 6-week exercise intervention, no other changes in bone microarchitecture or mechanical properties were found. |
