The cardiogenic fate is established as a bilateral heart field (HF) within the anterior mesoderm through an inductive inter-germ layer signaling interaction. Many genetic pathways responsible for fate specification and differentiation of the HF have been extensively studied. However, where cells of the HF originate, how they precisely arrive at bilateral HF, or how they receive fate specification cues, remains obscured. Using live imaging of both wild type and somatic trans-genetic embryos with molecular sensors, this proposal will identify a coupling of: axis inducing signals with HF precursor positioning in the PS (Aim 1), the earlier onset of bilateral patterning (Aim 2); and a direct cell-cell contact with HF fate specification signaling transfer (Aim 3). Taken together, the proposed study will establish a novel view for the importance of coordinated positioning and interactions in the PS and at the HF forming site to define ultimate cardiogenic fate.

Public Health Relevance

The heart is the first organ system to form and begin function during embryogenesis. This proposal will explore where heart precursor cells originate and how they are induced to form the heart at the correct embryonic position. Outcomes will establish a novel view how the embryo specifies the ultimate cardiogenic cell population.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
1R01HL153736-01
Application #
10033231
Study Section
Cardiovascular Differentiation and Development Study Section (CDD)
Program Officer
Schramm, Charlene A
Project Start
2020-08-28
Project End
2024-05-31
Budget Start
2020-08-28
Budget End
2021-05-31
Support Year
1
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94118