Pathological features of mitochondrial respiratory chain dysfunction

Thesis: Ph. D., Massachusetts Institute of Technology, Department of Biology, 2016.

Bibliographic Details
Main Author: Chen, Walter W
Other Authors: David M. Sabatini.
Format: Thesis
Language:eng
Published: Massachusetts Institute of Technology 2016
Subjects:
Online Access:http://hdl.handle.net/1721.1/104099
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author Chen, Walter W
author2 David M. Sabatini.
author_facet David M. Sabatini.
Chen, Walter W
author_sort Chen, Walter W
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description Thesis: Ph. D., Massachusetts Institute of Technology, Department of Biology, 2016.
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spelling mit-1721.1/1040992019-04-12T14:00:36Z Pathological features of mitochondrial respiratory chain dysfunction Chen, Walter W David M. Sabatini. Massachusetts Institute of Technology. Department of Biology. Massachusetts Institute of Technology. Department of Biology. Biology. Thesis: Ph. D., Massachusetts Institute of Technology, Department of Biology, 2016. This electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections. Cataloged from student-submitted PDF version of thesis. "June 2016." Includes bibliographical references. Mitochondria are essential organelles that carry out a multitude of important metabolic processes in mammalian organisms. These processes include ATP generation by the respiratory chain, aspartate synthesis by matrix aminotransferases, and long-chain fatty acid catabolism by the beta oxidation pathway. Given the role of mitochondria in maintaining cellular physiology, mitochondrial dysfunction often leads to disease. One major class of mitochondrial pathologies is caused by defects in the mitochondrial respiratory chain (RC). Yet while the genetic etiologies of these RC disorders are well-studied, the molecular defects that actually link RC dysfunction with impaired cellular viability are still unclear. In the work described here, we demonstrate that loss of mitochondrial membrane potential and aspartate contributes significantly to cellular pathology during RC dysfunction. In addition, we develop a novel method for rapidly isolating mitochondria and profiling their metabolite contents to study the changes in mitochondrial metabolism across various states of RC function. From this work, we find numerous alterations in matrix metabolites that had been previously unappreciated using traditional profiling of whole-cells and identify new metabolic abnormalities downstream of RC dysfunction. Collectively, this work uncovers distinct molecular events connecting RC pathology with impaired cellular viability and expands our understanding of the metabolic processes affected by RC dysfunction, thus opening up new areas for exploration. by Walter W. Chen. Ph. D. 2016-09-13T18:04:49Z 2016-09-13T18:04:49Z 2016 Thesis http://hdl.handle.net/1721.1/104099 958133195 eng M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. http://dspace.mit.edu/handle/1721.1/7582 171 pages application/pdf Massachusetts Institute of Technology
spellingShingle Biology.
Chen, Walter W
Pathological features of mitochondrial respiratory chain dysfunction
title Pathological features of mitochondrial respiratory chain dysfunction
title_full Pathological features of mitochondrial respiratory chain dysfunction
title_fullStr Pathological features of mitochondrial respiratory chain dysfunction
title_full_unstemmed Pathological features of mitochondrial respiratory chain dysfunction
title_short Pathological features of mitochondrial respiratory chain dysfunction
title_sort pathological features of mitochondrial respiratory chain dysfunction
topic Biology.
url http://hdl.handle.net/1721.1/104099
work_keys_str_mv AT chenwalterw pathologicalfeaturesofmitochondrialrespiratorychaindysfunction