PUBLICATION
An exclusive cellular and molecular network governs intestinal smooth muscle cell differentiation in vertebrates
- Authors
- Gays, D., Hess, C., Camporeale, A., Ala, U., Provero, P., Mosimann, C., Santoro, M.M.
- ID
- ZDB-PUB-170105-5
- Date
- 2017
- Source
- Development (Cambridge, England) 144(3): 464-478 (Journal)
- Registered Authors
- Gays, Dafne, Hess, Christopher, Mosimann, Christian, Santoro, Massimo
- Keywords
- lateral plate mesoderm, organogenesis, smooth muscle cells, zebrafish
- MeSH Terms
-
- Myocytes, Smooth Muscle/cytology*
- Myocytes, Smooth Muscle/metabolism
- Zebrafish Proteins/genetics
- Zebrafish Proteins/metabolism
- Morphogenesis
- PubMed
- 28049660 Full text @ Development
Abstract
Intestinal smooth muscle cells (iSMCs) are a critical component of the adult gastrointestinal (GI) tract and support intestinal differentiation, peristalsis, and epithelial homeostasis during development. Despite these critical roles, the origin of iSMCs and the mechanisms responsible for their differentiation and function remain fairly unknown in vertebrates. Here, using genetic lineage tracing in zebrafish, we demonstrated that iSMCs arise from the lateral plate mesoderm (LPM) in a stepwise process. Early during organogenesis, LPM cells progressively migrate ventral to the endoderm tube wrapping the developing gut. Concomitantly, the LPM differentiates by turning on early SMC markers. Combining pharmacological and genetic approaches, we show that TGF-β/Alk5 signaling drives the LPM ventral migration and commitment to an iSMC fate. The Alk5-dependent induction of zeb1a and foxo1a is required for this morphogenetic process: zeb1a is responsible to drive LPM migration around the gut, while foxo1a regulates LPM predisposition to iSMC differentiation. We further show that the three factors TGF-β, zeb1a, and foxo1a are tightly linked together by miR-145 In iSMC-committed cells, TGF-β induces the expression of miR-145 that in turn is able to downregulate zeb1a and foxo1a The absence of miR-145 results in only a slight reduction of iSMCs, which however still express mesenchymal genes yet fail to contract. Together, our data uncover a cascade of molecular events that govern distinct morphogenetic steps during the emergence and differentiation of vertebrate iSMCs.
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