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mab21-l3 regulates cell fate specification of multiciliate cells and ionocytes

Authors: 
Takahashi C, Kusakabe M, Suzuki T, Miyatake K, Nishida E
Citation: 
Nat Commun. 2015 Jan 19;6:6017. doi: 10.1038/ncomms7017
Abstract: 
Cell fate specifications of multiciliate cells (MCCs) and ionocytes are commonly suppressed by the Notch pathway in developing epithelia, but are governed by different master regulators, suggesting the existence of a common regulator linking the Notch pathway to both MCC and ionocyte specifications. Here we show that a mab21 family gene, mab21-l3, represents the missing link. In Xenopus embryonic epidermis, mab21-l3 expression is specifically found in MCCs and ionocytes and is downregulated by the Notch pathway. Knockdown of mab21-l3 in Xenopus downregulates both MCC-specific and ionocyte-specific master genes, resulting in drastic loss of MCCs and ionocytes. In mouse tracheal epithelial cells, mab21-l3 expression is also downregulated by the Notch pathway and is required for MCC differentiation. Moreover, conditional gain of function of mab21-l3 rescues Notch-induced loss of MCCs and ionocytes in Xenopus. These results indicate that mab21-l3 acts downstream of the Notch pathway in cell fate specifications of MCCs and ionocytes.
Epub: 
Not Epub
Organism or Cell Type: 
Xenopus
Delivery Method: 
microinjection