Intestinal disorders such as inflammatory bowel disease (IBD) and cancer frequently reflect dysregulated activity of crypt stem and progenitor cells. Relationships among these cells are presently coming into focus but it remains unclear how the key cell populations regulate lineage-specific genes to choose among alternative enterocyte and secretory cell fates. Intestinal crypt homeostasis most notably requires Notch and Wnt signaling, among other pathways. The two canonical signals cooperate to promote cell replication, but whereas Wnt signaling promotes intestinal secretory cell differentiation, Notch signaling favors enterocyte differentiation at the expense of secretory cells;the basis for these differences is unknown. Notch inhibits expression of transcription factor Atoh1 (Math1), whose activity or absence seems sufficient to allocate cell lineages by the evolutionarily conserved process of lateral inhibition. Manipulation of GI signaling pathways for clinical application will require a deeper appreciation of underlying principles and mechanisms to identify therapeutic targets that will least disrupt normal digestive physiology. This proposal applies innovative methods to isolate mouse intestinal crypt progenitors and to study in fresh detail the epigenetic and transcriptional basis of cell fate decisions.
In Specific Aim 1 we will identify lineage- restricted enhancer elements and genome-wide binding sites for Atoh1 in purified secretory progenitors, with the view to determine mechanisms for its potent ability to specify the full secretory lineage. We will analyze Atoh1 occupancy at cis-elements with respect to nucleosome-histone dynamics in the transition from stem cells to committed progenitors. We will define Atoh1 target genes and investigate the roles of such genes in human pathology specimens showing aberrant secretory differentiation, including IBD samples and mucinous/signet-ring colorectal cancer. To explain the multi-faceted relationship of Wnt and Notch signaling in gut epithelial progenitors, we will test the hypothesis that Atoh1 steers the Wnt-effector transcription factor Tcf4 away from cis-elements of proliferative genes and toward those of a Wnt- dependent secretory cell program.
In Specific Aim 2 we propose to isolate the earliest stem-cell progeny, bipotential progenitors able to differentiate into secretory cells or enterocytes. We will study the epigenetic basis and Atoh1 dependencies for their subsequent commitment to a single fate. We will test the hypothesis that Atoh1 controls histone marks and nucleosome dynamics not only to activate secretory cis- elements but also to repress enterocyte genes. Using genetic mouse models and up-to-date approaches in epigenomic and transcription factor analysis, we propose experiments that will give clear answers and test specific predictions and hypotheses. These studies collectively address fundamental questions, explore developmental signaling and regulatory mechanisms in molecular detail in vivo, test specific and cogent hypotheses, and will contribute toward improved understanding and treatment of common GI disorders.
The intestinal lining is refreshed daily, requiring continual generation of new cells;this process is defective in diseases such as inflammatory bowel disease (IBD) and cancer. Two signaling pathways, Wnt and Notch, implement key decisions about the choice of which type of new cells to produce. Understanding how these crucial pathways act to determine cell fate and behaviors has important implications not only for forward-looking treatments for IBD and cancer, but also more generally for stem cell biology and the burgeoning field of regenerative medicine. New tissues can only be engineered in the laboratory for therapeutic replacement after we understand how cells make fundamental decisions about their identities. We propose molecular and genetic studies to investigate the precise mechanisms by which signaling pathways affect DNA to influence the variety of intestinal cells that secretes mucus or hormones. These studies will help lay a foundation for new approaches toward treatment of common and disabling digestive tract disorders.
|Kim, Tae-Hee; Li, Fugen; Ferreiro-Neira, Isabel et al. (2014) Broadly permissive intestinal chromatin underlies lateral inhibition and cell plasticity. Nature 506:511-5|
|San Roman, Adrianna K; Jayewickreme, Chenura D; Murtaugh, L Charles et al. (2014) Wnt secretion from epithelial cells and subepithelial myofibroblasts is not required in the mouse intestinal stem cell niche in vivo. Stem Cell Reports 2:127-34|
|Shivdasani, Ramesh A (2014) Radiation redux: reserve intestinal stem cells miss the call to duty. Cell Stem Cell 14:135-6|
|Kim, Tae-Hee; Escudero, Silvia; Shivdasani, Ramesh A (2012) Intact function of Lgr5 receptor-expressing intestinal stem cells in the absence of Paneth cells. Proc Natl Acad Sci U S A 109:3932-7|
|Woo, Janghee; Miletich, Isabelle; Kim, Byeong-Moo et al. (2011) Barx1-mediated inhibition of Wnt signaling in the mouse thoracic foregut controls tracheo-esophageal septation and epithelial differentiation. PLoS One 6:e22493|
|Kim, Byeong-Moo; Woo, Janghee; Kanellopoulou, Chryssa et al. (2011) Regulation of mouse stomach development and Barx1 expression by specific microRNAs. Development 138:1081-6|
|Kim, Tae-Hee; Shivdasani, Ramesh A (2011) Notch signaling in stomach epithelial stem cell homeostasis. J Exp Med 208:677-88|
|Kim, Tae-Hee; Kim, Byeong-Moo; Mao, Junhao et al. (2011) Endodermal Hedgehog signals modulate Notch pathway activity in the developing digestive tract mesenchyme. Development 138:3225-33|
|San Roman, Adrianna K; Shivdasani, Ramesh A (2011) Boundaries, junctions and transitions in the gastrointestinal tract. Exp Cell Res 317:2711-8|
|Kim, Tae-Hee; Shivdasani, Ramesh A (2011) Genetic evidence that intestinal Notch functions vary regionally and operate through a common mechanism of Math1 repression. J Biol Chem 286:11427-33|
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