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Title page for ETD etd-03282008-155041

Type of Document Dissertation
Author Langworthy, Melissa Marie
URN etd-03282008-155041
Title The role of NFATc1 in proximal tubule injury and repair
Degree PhD
Department Cell and Developmental Biology
Advisory Committee
Advisor Name Title
Christopher Wright Committee Chair
Chin Chiang Committee Member
H. Scott Baldwin Committee Member
Mark de Caestecker Committee Member
Raymond Harris Committee Member
  • Kidneys -- Wounds and injuries
  • Kidney tubules
  • progenitor cells
  • kidney
  • acute kidney injury
  • mercury
  • regeneration
  • Transcription factors -- Physiology
  • NFATC Transcription Factors
Date of Defense 2008-02-02
Availability unrestricted
Recovery from acute kidney injury (AKI) requires renal tubule cell regeneration. The population of cells that repair the damaged proximal tubule epithelial cells (PTC) has been proposed to be derived from an external population circulating in the blood stream, an adjacent less-injured renal cell population, or a resident self-renewing PTC population. The identification of renal progenitor cells has been difficult because such a population remains phenotypically indistinguishable from their terminally differentiated counterparts and would require creation and characterization of transgenic reporters.

For my dissertation research, I investigated the role of NFATc1 in PTCs. A single dose of mercuric chloride (HgCl2) was administered to induce AKI. The data presented here show that NFATc1 plays a role in PTC regeneration following AKI and genetic and/or pharmacologic attenuation of NFATc1 results in increased PTC apoptosis, increased serum creatinine, decreased proliferation, and even death.

Using novel NFATc1 transgenic lines that reports activation of an NFATc1 enhancer domain important for autoamplification of NFATc1, we identified a subpopulation of proximal tubule progenitor cells that were resistant to apoptosis following HgCl2 injury. Lineage analysis documented that the NFATc1 labeled PTCs proliferate to repair the damaged proximal tubule segment. The expression profile of this labeled cell population and their labeled progeny was compared to unlabeled PTCs and showed that the labeled population were differentiated proximal tubule cells that had increased transcription of pluripotent stem cell and tubule development markers. To our knowledge, the delayed regeneration after AKI is the first example of a phenotype identified in the Nfatc1+/- mouse and proposes a role for NFATc1 in the regeneration of injured proximal tubule cells by as resident population of progenitor proximal tubules accentuated by NFATc1 expression.

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