Studies of Direct Pluripotent Stem Cell Programming. It is widely known that the induction of cell fates during embryogenesis is orchestrated through the action of developmental signals, such as growth factors (1). Proper exposure to these signals leads to the normal patterning and growth of the embryo. We recently proposed that one outcome of this signaling, cell type differentiation, involves among other factors alignment of the transcriptional or epigenetic state, which determines the cell type to be specified, and 2. It's appropriate cell cycle state, which affects the rate of differentiation (2). Within some limits, t may be possible to perturb the normal process of differentiation and achieve differentiated states more rapidly and through pathways that do not occur naturally. This study of the alteration of the normal differentiation process helps us understand the elements required for cell fate and cannot be understood by studying only normal embryonic differentiation. Furthermore, these altered pathways of differentiation could lead to useful approaches for regenerative medicine.
The aim of this proposal is to develop and to better understand the pathway independence of differentiation and the special role of transcriptional regulators and cell cycle regulation. We will address three important issues: 1. What are the underlying molecular changes that underlie altered pathways of differentiation, 2. In terms of different cell types, how widely applicable are the methods we developed, and 3. Can these discoveries in mouse ES cells be demonstrated in human.

Public Health Relevance

Stem cell therapy holds the promise for treating a large number of human diseases. In order to achieve this promise, gaining a better understanding of stem cell differentiation and translating this knowledge into beneficial technologies is essential. In this proposal, we aim to develop and understand a new approach to pluripotent stem cell differentiation called direct programming, and expand its use from mouse to human.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21HD087723-01
Application #
9091998
Study Section
Development - 2 Study Section (DEV2)
Program Officer
Mukhopadhyay, Mahua
Project Start
2016-03-04
Project End
2018-02-28
Budget Start
2016-03-04
Budget End
2017-02-28
Support Year
1
Fiscal Year
2016
Total Cost
$211,875
Indirect Cost
$86,875
Name
Harvard Medical School
Department
Biology
Type
Schools of Medicine
DUNS #
047006379
City
Boston
State
MA
Country
United States
Zip Code
02115
Briggs, James A; Weinreb, Caleb; Wagner, Daniel E et al. (2018) The dynamics of gene expression in vertebrate embryogenesis at single-cell resolution. Science 360:
Briggs, James Alexander; Li, Victor C; Lee, Seungkyu et al. (2017) Mouse embryonic stem cells can differentiate via multiple paths to the same state. Elife 6: