Role of mTORC1 in ventilator induced lung injury

mTORC1 在呼吸机所致肺损伤中的作用

• 批准号: 8916788
• 负责人: Joshua A Englert
• 金额: $ 5.2万
• 依托单位: BRIGHAM AND WOMEN'S HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-09-01 至 2015-10-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8916788
• 关键词: Active Sites; Acute Lung Injury; Adult Respiratory Distress Syndrome; Advisory Committees; Affect; Alveolar; Area; Autophagocytosis; Biochemical; Biology; Capillary Permeability; Cells; Complex; Critical Care; Data; Development; Development Plans; Disease; Drug Targeting; Embryo; Environmental air flow; Epithelial Cells; FDA approved; Genetic; Goals; Gray unit of radiation dose; Heterogeneity; Histologic; In Vitro; Inflammation; Inflammation Mediators; Inflammatory; Inflammatory Response; Injury; Kinetics; Lead; Life; Ligation; Lung; Measures; Mechanical ventilation; Mechanics; Medicine; Mentors; Modeling; Molecular; Morbidity - disease rate; Mus; Pathologic; Pathway interactions; Patients; Physicians; Physiology; Play; Principal Investigator; Process; Puncture procedure; Role; Scientist; Sepsis; Signaling Protein; Sirolimus; Stress; Stretching; Syndrome; Testing; Therapeutic; Tidal Volume; Training; Training Programs; Tuberous sclerosis protein complex; Ventilator; Ventilator-induced lung injury; base; career development; cell growth regulation; clinically relevant; human FRAP1 protein; improved; in vivo; inhibition of autophagy; inhibitor/antagonist; lung injury; mTOR inhibition; mortality; new therapeutic target; novel; novel strategies; prevent; protein complex; public health relevance; response; response to injury; septic; skills; targeted treatment

DESCRIPTION (provided by applicant): The acute respiratory distress syndrome (ARDS) affects more than 200,000 patients in the US annually and is associated with significant morbidity and mortality rates approaching 40%. The mainstay of supportive treatment for this condition is mechanical ventilation. While frequently life-saving, mechanical ventilation can also exacerbate pre-existing lung injury and cause de novo injury, known as ventilator induced lung injury (VILI). Limiting lung stretch in patients by using low tidal volume ventilation is one of th few strategies that has been shown to decrease mortality in patients with ARDS. Although ventilator management for patients with ARDS has improved, factors such as the regional heterogeneity of the lung injury can lead to persistent injury even with low tidal volume ventilation. To date, no therapies targeted to the specific pathophysiologic mechanisms of lung injury are available for the treatment of patients with ARDS or VILI. Our preliminary data demonstrate that mTOR complex 1 (mTORC1), a multi-protein complex that plays a key role in the regulation of cell growth and response to stress is activated in epithelial cells in a clinicaly relevant murine model combining sepsis from cecal ligation and puncture and VILI with modest tidal volumes (CLP/VILI). Furthermore, we show that mTORC1 activation in CLP/VILI corresponds with impaired autophagy and that pharmacologic mTORC1 inhibition (which increases autophagy) is protective. We hypothesize that mTORC1 activation in lung epithelial cells plays a key role in the development of lung injury in response to mechanical ventilation. To investigate this hypothesis we have proposed the following specific aims: 1) to determine the effects of genetic mTORC1 activation on the development of lung injury in the CLP/VILI model; 2) to determine the effects of pharmacologic mTORC1 inhibition in the CLP/VILI model; 3) to determine the role of stretch induced mTORC1 activation in modulating autophagy and downstream pro-inflammatory pathways in lung epithelial cells. The principal investigator has developed a five-year training program under the guidance of his mentors Drs. Rebecca Baron and Augustine M.K. Choi to develop the skills necessary to become a successful physician- scientist in the field of pulmonary and critical care medicine. The candidate's training will also e overseen by an advisory committee with expertise related to key areas of this proposal including acute lung injury, mTOR biology, and mechanotransduction. The proposed career development plan will provide the additional training necessary to achieve principal investigator's ultimate goal of becoming an independent physician-scientist studying the biologic basis of ARDS and VILI.

描述（由申请方提供）：急性呼吸窘迫综合征（ARDS）每年影响美国超过20万例患者，并与接近40%的显著发病率和死亡率相关。这种情况的支持性治疗的支柱是机械通气。虽然经常挽救生命，但机械通气也可能加剧先前存在的肺损伤并导致新生损伤，称为呼吸机诱导的肺损伤（VILI）。通过使用低潮气量通气限制患者的肺伸展是已被证明可降低ARDS患者死亡率的少数策略之一。尽管ARDS患者的呼吸机管理已得到改善，但即使采用低潮气量通气，肺损伤的区域异质性等因素仍可能导致持续性损伤。迄今为止，没有针对肺损伤的特定病理生理机制的疗法可用于治疗患有ARDS或VILI的患者。我们的初步数据表明，mTOR复合物1（mTORC 1），一种在调节细胞生长和应激反应中起关键作用的多蛋白复合物，在临床相关的小鼠模型中的上皮细胞中被激活，该模型结合了盲肠结扎和穿刺的脓毒症和具有适度潮气量的VILI（CLP/VILI）。此外，我们发现mTORC 1在CLP/VILI中的激活与受损的自噬相对应，并且药理学mTORC 1抑制（增加自噬）具有保护作用。我们推测肺上皮细胞中mTORC 1的激活在机械通气引起肺损伤的发展中起关键作用。为了研究这一假设，我们提出了以下具体目标：1）确定遗传mTORC 1激活对CLP/VILI模型中肺损伤发展的影响; 2）确定药理学mTORC 1抑制在CLP/VILI模型中的影响; 3）确定牵张诱导的mTORC 1激活在调节肺上皮细胞自噬和下游促炎途径中的作用。首席研究员在他的导师Rebecca Baron博士和Augustine M.K.博士的指导下制定了一个为期五年的培训计划。崔发展必要的技能，成为一个成功的医生，科学家在肺部和重症监护医学领域。候选人的培训也将由一个咨询委员会监督，该委员会具有与该提案的关键领域相关的专业知识，包括急性肺损伤，mTOR生物学和机械转导。拟议的职业发展计划将提供必要的额外培训，以实现主要研究者的最终目标，即成为一名独立的医生-科学家，研究ARDS和VILI的生物学基础。