Each year, 9.6% of infants, 13 million worldwide, are born with low birth weight with a mortality rate 20 times higher than in normal babies. Most of these preterm infants as well as some term babies have abnormal or no pulmonary surfactant, a lipid-protein mixture secreted by alveolar type II epithelial (AEII) cells. When surfactant functio is abnormal, the lung partially collapses hindering gas exchange, a severe condition that can lead to death. Patients suffering from surfactant deficiency invariably require mechanical ventilation. During the last decade, variable ventilation (VV) emerged and proved to be superior to conventional ventilation (CV). In VV, tidal volumes (VT) are varied on a breath-by-breath basis such that VT is drawn from a distribution optimized to achieve best alveolar recruitment. Previously, we found that in normal guinea pigs, VV increased surfactant concentration at the air-liquid interface due to increased surfactant release that we directly proved by stretching primary AEII cells in culture using a variable stretch pattern. Since mechanical stretch is perhaps the most potent stimulant for surfactant release by AEII cells, the stretch pattern applied to AEII cells in vivo might have a crucial importance in the outcome of ventilation of infants. Hence, we hypothesize that during conditions of surfactant deficiency, the application of VV will lead to enhanced surfactant production and secretion with improved lung function and gas exchange compared to CV. To test this hypothesis, we set up 3 aims: 1) To study the signaling pathways of variable stretch-induced surfactant metabolism including gene regulation and release by AEII cells in culture isolated from healthy baby rabbits and surfactant deficient preterm rabbits. 2) To determine the optimal conditions under which VV enhances surfactant gene upregulation and release by AEII cells in healthy baby rabbits and surfactant deficient preterm rabbits and lambs. 3) To test in baby rabbits and lambs the effectiveness of a novel mechanical assay which non-invasively monitors the organ level functionality of the surfactant system. Studies will be carried out at the cell, tissue and organ level to reveal how VV enhances surfactant secretion through regulating specific fusion pore proteins. If the results confirm our hypothesis, the implications are truly important with significant impact on neonatal care. For example, we will uncover the cellular mechanism of variable stretch-induced surfactant production and release. The treatment will not require exogenous surfactant therapy. Rather, using a simple mechanical perturbation (tuned variability in VT), we will stimulate AEII cells in vivo to generate more surfactant, a procedure we call endogenous surfactant therapy. The method is inherently safe as there is no radiation, chemical treatment or any other harm associated with moderately varying VT. Thus, we expect to start translating the technology to clinical practice toward the end of the award period. In conclusion, this simple mechanical intervention may reduce the morbidity and mortality associated with surfactant deficiency in infants and children by appropriately steering the body's endogenous response.
Each year, millions of infants worldwide are born with low birth weight that results in abnormal lung function and high mortality rate. Using a simple mechanical perturbation during mechanical ventilation that is inherently safe, we aim to test a novel method that has the potential to reduce the morbidity and mortality of these infants by appropriately steering the body's own biological response.
| Hamlington, Katharine L; Bates, Jason H T; Roy, Gregory S et al. (2018) Alveolar leak develops by a rich-get-richer process in ventilator-induced lung injury. PLoS One 13:e0193934 |
| Smith, Bradford J; Bartolak-Suki, Elizabeth; Suki, Bela et al. (2017) Linking Ventilator Injury-Induced Leak across the Blood-Gas Barrier to Derangements in Murine Lung Function. Front Physiol 8:466 |
| Alves, Calebe; Araújo, Ascanio D; Oliveira, Cláudio L N et al. (2016) Homeostatic maintenance via degradation and repair of elastic fibers under tension. Sci Rep 6:27474 |
| Yi, Eunice; Sato, Susumu; Takahashi, Ayuko et al. (2016) Mechanical Forces Accelerate Collagen Digestion by Bacterial Collagenase in Lung Tissue Strips. Front Physiol 7:287 |
| Suki, Béla; Parameswaran, Harikrishnan; Imsirovic, Jasmin et al. (2016) Regulatory Roles of Fluctuation-Driven Mechanotransduction in Cell Function. Physiology (Bethesda) 31:346-58 |
| Sanders, Kenton M; Kito, Yoshihiko; Hwang, Sung Jin et al. (2016) Regulation of Gastrointestinal Smooth Muscle Function by Interstitial Cells. Physiology (Bethesda) 31:316-26 |
| Imsirovic, Jasmin; Wellman, Tyler J; Mondoñedo, Jarred R et al. (2015) Design of a Novel Equi-Biaxial Stretcher for Live Cellular and Subcellular Imaging. PLoS One 10:e0140283 |
| Takahashi, Ayuko; Bartolák-Suki, Erzsébet; Majumdar, Arnab et al. (2015) Changes in respiratory elastance after deep inspirations reflect surface film functionality in mice with acute lung injury. J Appl Physiol (1985) 119:258-65 |
| Suki, Béla; Hubmayr, Rolf (2014) Epithelial and endothelial damage induced by mechanical ventilation modes. Curr Opin Crit Care 20:17-24 |
