Pompe disease (PD), is a rare autosomal recessive disorder caused by a deficiency of acid alpha-glucosidase (GAA) – a lysosomal enzyme that hydrolyzes glycogen. Recent findings from our laboratory identified the impact of GAA deficiency and glycogen accumulation in alveolar type 1 and type 2 (AT1 and AT2) cells. Specifically, we found that GAA deficiency in PD resulted in engorged lysosomes which significantly disrupted AT1 and AT2 cellular architecture. Lysosomes are an essential component of autophagy which is important for maintaining cellular homeostasis. Building on these novel findings, we are seeking a post-doctoral fellow who will work on a project that assesses the mechanisms by which a lack of GAA results in disrupted alveolar remodeling and repair after lung injury. Specifically, we are looking for a post-doctoral fellow who has expertise in lung inflation and harvesting, lung histology and sectioning, and immunohistochemistry. Some expertise in single-cell RNA sequencing is also preferable.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Job Type
Full-time
Education Level
Ph.D. or professional degree
Number of Employees
5,001-10,000 employees