The mammalian heart forms early in embryogenesis, and defects in its formation are at the root of congenital heart defects (CHDs), affecting 1-2% of live births. In adults, heart disease is the number one killer in the Western world, resulting in a considerable health burden. Understanding the building blocks of the heart is critical to define the etiology of CHDs and to create novel cell-based regeneration strategies to treat heart disease. Identifying and isolating cardiac precursors from pluripotent cells would allow characterization and expansion of cardiac cells for regenerative strategies. We identified expression of Smarcd3 (also known as Baf60c) as a candidate early marker of a prespecified mesoderm population that gives rise predominantly to cells of the developing heart. Using transgenic reporter assays and inducible Cre-mediated lineage tracing, we showed early expression of Smarcd3 in anterior mesoderm of the mouse is a specific marker of the earliest specified cardiac precursors, preceding expression of any other cardiac precursor marker. We hypothesize that Smarcd3 marks the earliest specific cardiac progenitors in the mouse embryo, and that this specialized mesodermal population has distinct properties that lead to preferential differentiation into cardiomyocytes. We will test this hypothesis in three Specific Aims.
Aim 1 : To define the early cardiac lineage marked by Smarcd3 expression. Using transgenic reporter lines, we will delineate the relationship between the Smarcd3 lineage and previously characterized cardiac lineages. We will use inducible Cre labeling, combined with multicolor "rainbow" reporter mice to define the early Smarcd3 lineage and the clonal relationships between its descendents. Using fluorescent reporter transgenic mouse lines, we will purify Smarcd3-expressing progenitors Aim 2. To determine the transcriptional and signaling pathways that activate early Smarcd3 expression. In this aim, we will define the genetic and signaling inputs that direct Smarcd3 expression in early cardiac progenitors. We will use transient transgenesis in mouse and differentiating ES cells to define the transcriptional inputs that activate Smarcd3 expression. Using transgenic ES cells expressing EGFP under control of the Smarcd3 regulatory region, we will identify the sets of signaling inputs that direct activation of Smarcd3 in this early population of cardiac precursors.
Aim 3 : To define signaling pathways that lead to cardiac differentiation of the early cardiac lineage. We will determine the importance of BMP and Wnt signaling in the differentiation of cardiac tissue from embryonic mesoderm, as well as the temporal requirement for these pathways. The results will be critical to understand the inductive cues required for cardiac differentiation. The knowledge generated from this study will be crucial to our understanding of the earliest fate decisions that lead to the formation of te heart.

Public Health Relevance

Congenital heart defects are among the most common and most devastating birth defects in humans, occurring in about 1% of live births. Despite this, we have little knowledge about where the heart arises in embryonic development. Our proposed studies will lead to discoveries about the fundamental origins of the heart, and how the earliest cardiac progenitors are mobilized to make a heart. Furthermore, our research will allow us to identify and isolate cardiac precursors from stem cells.

Agency
National Institute of Health (NIH)
Type
Research Project (R01)
Project #
5R01HL114948-02
Application #
8692013
Study Section
Cardiovascular Differentiation and Development Study Section (CDD)
Program Officer
Burns, Kristin
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
2014
Total Cost
Indirect Cost
Name
J. David Gladstone Institutes
Department
Type
DUNS #
City
San Francisco
State
CA
Country
United States
Zip Code
94158