| First Author | van den Berg M | Year | 2022 |
| Journal | Int J Mol Sci | Volume | 23 |
| Issue | 24 | PubMed ID | 36555335 |
| Mgi Jnum | J:335092 | Mgi Id | MGI:7412178 |
| Doi | 10.3390/ijms232415689 | Citation | van den Berg M, et al. (2022) Rbm20(DeltaRRM) Mice, Expressing a Titin Isoform with Lower Stiffness, Are Protected from Mechanical Ventilation-Induced Diaphragm Weakness. Int J Mol Sci 23(24) |
| abstractText | Diaphragm weakness frequently develops in mechanically ventilated critically ill patients and is associated with increased morbidity, including ventilator weaning failure, mortality, and health care costs. The mechanisms underlying diaphragm weakness are incompletely understood but may include the elastic properties of titin, a giant protein whose layout in the muscle's sarcomeres makes it an ideal candidate to sense ventilation-induced diaphragm unloading, resulting in downstream signaling through titin-binding proteins. In the current study, we investigated whether modulating titin stiffness affects the development of diaphragm weakness during mechanical ventilation. To this end, we ventilated genetically engineered mice with reduced titin stiffness (Rbm20(DeltaRRM)), and robust (Ttn(DeltaIAjxn)) or severely (Ttn(Delta112-158)) increased titin stiffness for 8 h, and assessed diaphragm contractility and protein expression of titin-binding proteins. Mechanical ventilation reduced the maximum active tension of the diaphragm in WT, Ttn(DeltaIAjxn) and Ttn(Delta112-158) mice. However, in Rbm20(DeltaRRM) mice maximum active tension was preserved after ventilation. Analyses of titin binding proteins suggest that muscle ankyrin repeat proteins (MARPs) 1 and 2 may play a role in the adaptation of the diaphragm to mechanical ventilation, and the preservation of diaphragm contractility in Rbm20(DeltaRRM) mice. Thus, Rbm20(DeltaRRM) mice, expressing titin isoforms with lower stiffness, are protected from mechanical ventilation-induced diaphragm weakness, suggesting that titin elasticity may modulate the diaphragm's response to unloading during mechanical ventilation. |
