PhD Proposal by Andre Norfleet

Event Details
  • Date/Time:
    • Friday June 12, 2020
      1:00 pm - 3:00 pm
  • Location: REMOTE: BLUE JEANS
  • Phone:
  • URL: BlueJeans
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  • Fee(s):
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Summaries

Summary Sentence: Metabolic and Bioelectric Crosstalk in Directed Differentiation and Spatial Patterning of iPSC-derived Cardiomyocytes

Full Summary: No summary paragraph submitted.

Andre Norfleet

BioE PhD Proposal Presentation

 

Date: June 12th, 2020

Time: 1:00 PM

Location: https://bluejeans.com/291598154

 

Committee Members:

- Dr. Melissa Kemp (Advisor, BME, Georgia Tech)

- Dr. Manu Platt  (BME, Georgia Tech)

- Dr. Eberhard Voit (BME, Georgia Tech)

- Dr. Ravi Kane (ChBE, Georgia Tech)

- Dr. Craig Forest (ME, Georgia Tech)

- Dr. Sung-Jin Park (BME, Georgia Tech)

 

Metabolic and Bioelectric Crosstalk in Directed Differentiation and Spatial Patterning of iPSC-derived Cardiomyocytes

 

Bioelectric cell physiology and signaling have recently received much attention for their exerted control over multicellular regenerative and developmental patterning outcomes. More specifically, resting membrane potentials, ionic currents, and long-range electric fields define bioelectric signals that dictate non-excitable cell developmental patterning. Understanding bioelectric system dynamics and their relation to downstream developmental pattern trajectories would provide engineers the ability to design and manipulate multicellular systems to specified phenotypes. Efforts to understand these mechanisms are complicated because the Vmem-determining ion channels and gap junctions are also modulated by Vmem, resulting in complex system feedback. Development of a bioelectric computational simulation platform enables a realistic bottom-up bioelectric modeling approach in which the coordinated dynamics of passive and active ion fluxes dictate spatiotemporal bioelectric patterning dynamics. The overall objective of this project is to determine the role of ionic fluxes in the creation and maintenance spatiotemporal bioelectric patterns present in iPSC multicellular clusters. The central hypothesis is that metabolism influences bioelectrical patterning through pH, ATP, and cell cycle effects that direct subsequent multicellular properties during iPSC-cardiomyocyte differentiation. Ultimately, the objective of this project as executed in three aims will relate bioelectric signaling cues, cell metabolism, and intercellular communication to downstream spatiotemporal phenotypic trajectories and will further provide a foundational basis for assisted control interventions of spatiotemporal bioelectric dynamic outcomes and downstream phenotypic trajectories.

 

Additional Information

In Campus Calendar
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Graduate Studies

Invited Audience
Faculty/Staff, Public, Graduate students, Undergraduate students
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Other/Miscellaneous
Keywords
Phd proposal
Status
  • Created By: Tatianna Richardson
  • Workflow Status: Published
  • Created On: Jun 2, 2020 - 4:59pm
  • Last Updated: Jun 2, 2020 - 4:59pm