Toward Xeno-free Stem Cell Culture: Nanofiber-directed Differentiation of mESC to Neurons

Information

  • Research Project
  • 8812048
  • ApplicationId
    8812048
  • Core Project Number
    R15GM113155
  • Full Project Number
    1R15GM113155-01
  • Serial Number
    113155
  • FOA Number
    PA-13-313
  • Sub Project Id
  • Project Start Date
    1/1/2015 - 9 years ago
  • Project End Date
    12/31/2017 - 6 years ago
  • Program Officer Name
    HAYNES, SUSAN R.
  • Budget Start Date
    1/1/2015 - 9 years ago
  • Budget End Date
    12/31/2017 - 6 years ago
  • Fiscal Year
    2015
  • Support Year
    01
  • Suffix
  • Award Notice Date
    12/29/2014 - 9 years ago
Organizations

Toward Xeno-free Stem Cell Culture: Nanofiber-directed Differentiation of mESC to Neurons

? DESCRIPTION: The use of xenogenic, costly, and complicated culture media and substrates during stem cell expansion and differentiation procedures has greatly limited their widespread use and translational relevance. To address these barriers, we have developed a synthetic nanofiber substrate that induces differentiation of mouse embryonic stem cells to neural progenitors within 1 day. Our proposed nanofibers use combinations of topography, alignment, and the tethering of up to three individually bioactive peptides where the presentation and concentration can be controlled precisely to influence cell membrane signaling interactions. Therefore, this proposal seeks to develop this multi-peptide tethered culture substrate for the directed differentiation and maturation of neurons and glia. We are uniquely positioned to develop a synthetic culture substrate capable of providing multiple functionalization sites for directed mouse embryonic stem cell differentiation; no other group to date offers more than 1 tethered peptide functionalization site. In this R15 proposal, we will direct stem cell differentiation by (i) characterizing the impact of surface-tethered bioactive molecules on neural lineage commitment (glial or neuronal) differentiation and maturity, and (ii) directing differentiation of mESCs into neural lineages via controlled surface interaction rather than soluble factors. The outcomes of these two aims will provide a novel, synthetic culture substrate for differentiation and long-term culture of mature neural cells. These outcomes have broad implications, as these culture substrates could be further modified to control the differentiation and maturity of other lineages. The PIs have excellent track records with research training, with the majority of the undergraduate students trained in their laboratories advancing into research-based, health-related graduate programs. If funded, the proposed project would significantly enhance the research environment in two colleges at The University of Akron. Both PIs have actively integrated undergraduates into their research laboratories, resulting in 18 co-authored papers (including 5 first-authored papers) over the past 5 years.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R15
  • Administering IC
    GM
  • Application Type
    1
  • Direct Cost Amount
    248915
  • Indirect Cost Amount
    124458
  • Total Cost
    373373
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    999
  • Ed Inst. Type
    BIOMED ENGR/COL ENGR/ENGR STA
  • Funding ICs
    NIGMS:373373\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    UNIVERSITY OF AKRON
  • Organization Department
    BIOMEDICAL ENGINEERING
  • Organization DUNS
    045207552
  • Organization City
    AKRON
  • Organization State
    OH
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    443250001
  • Organization District
    UNITED STATES