The bioelectrics of axis determination during zebrafish embryonic development

Information

  • Research Project
  • 9787806
  • ApplicationId
    9787806
  • Core Project Number
    R15HD099028
  • Full Project Number
    1R15HD099028-01
  • Serial Number
    099028
  • FOA Number
    PAR-18-834
  • Sub Project Id
  • Project Start Date
    8/1/2019 - 5 years ago
  • Project End Date
    7/31/2022 - 2 years ago
  • Program Officer Name
    MUKHOPADHYAY, MAHUA
  • Budget Start Date
    8/1/2019 - 5 years ago
  • Budget End Date
    7/31/2022 - 2 years ago
  • Fiscal Year
    2019
  • Support Year
    01
  • Suffix
  • Award Notice Date
    7/30/2019 - 5 years ago
Organizations

The bioelectrics of axis determination during zebrafish embryonic development

PROJECT SUMMARY Bioelectric mechanisms are emerging to be novel regulators of organ specification, growth and patterning during normal as well as regenerative development of organisms. Bioelectric properties of cells are determined by membrane localized channels that regulate entry of charged ions. Our interest in this topic stems from original findings that indicate membrane potentials of cells in gastrula stage zebrafish embryos appear to be in different states over distinct regions of the embryo. We are interested in understanding how these distinct bioelectric states may be generated and what is their significance. Gastrulation is a complex developmental stage when the dorsal-ventral and animal-vegetal axes are specified and cells begin to acquire specific fates. During this stage diverse morphogens and their effectors interact with each other to restrict their zones of influence and induce cell differentiation. We have determined that phenotypes induced by chemical inhibition of FGF by SU 5402 could be rescued by global increase in membrane depolarization across the embryo. We hypothesize that modulation of membrane potential could be altering the threshold for the specific inhibited FGF effector. To dissect this our project aims to define whether there is any specific membrane channel that is regulating a FGF effector or conversely and whether there is a membrane channel being regulated by FGF. To achieve our desired aims in a systematic manner, we first propose to characterize the pattern of voltage membrane potentials across the zebrafish gastrula over time with voltage sensitive dyes and the use of genetically encoded voltage indicators. We then plan to define the specific ion transporters mediating these bioelectric patterns as well as determine if they can influence the expression of core morphogenetic pathways during axis determination. Lastly, we will interrogate the interactions that bioelectric signaling has with Fgf signaling during axis determination and elongation. Most importantly, this study will be primarily accomplished with the support of undergraduate researchers who are all women and 50% of who first generation or researchers of color.

IC Name
EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT
  • Activity
    R15
  • Administering IC
    HD
  • Application Type
    1
  • Direct Cost Amount
    300000
  • Indirect Cost Amount
    156600
  • Total Cost
    456600
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    865
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NICHD:456600\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    SMITH COLLEGE
  • Organization Department
    BIOLOGY
  • Organization DUNS
    066989427
  • Organization City
    NORTHAMPTON
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    010636304
  • Organization District
    UNITED STATES