Transcription factor FoxO1 regulates myoepithelial cell diversity and growth

• Published in: Scientific reports Vol. 14; no. 1; p. 1069
• Main Authors: Tokumasu, Rino, Yasuhara, Rika, Kang, Seya, Funatsu, Takahiro, Mishima, Kenji
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 11.01.2024; Nature Publishing Group; Nature Portfolio
• Subjects: 631/136/142; 631/136/2086/1986; Animals; Cell adhesion molecules; Cell cycle; Cell growth; Cell proliferation; Chromatin; Ectodysplasin; Ectodysplasins - genetics; Epithelial Cells - metabolism; Exocrine glands; FOXO1 protein; Humanities and Social Sciences; Immunoprecipitation; Mesenchyme; Mice; multidisciplinary; Nucleotide sequence; Receptors, Tumor Necrosis Factor - metabolism; Saliva; Salivary gland; Salivary Gland Neoplasms - metabolism; Science; Science (multidisciplinary); Sequence analysis; Submandibular Gland - metabolism; Transcription factors; Transcription Factors - metabolism; Xedar Receptor - metabolism
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-51619-1

Salivary gland myoepithelial cells regulate saliva secretion and have been implicated in the histological diversity of salivary gland tumors. However, detailed functional analysis of myoepithelial cells has not been determined owing to the few of the specific marker to isolate them. We isolated myoepithelial cells from the submandibular glands of adult mice using the epithelial marker EpCAM and the cell adhesion molecule CD49f as indicators and found predominant expression of the transcription factor FoxO1 in these cells. RNA-sequence analysis revealed that the expression of cell cycle regulators was negatively regulated in FoxO1-overexpressing cells. Chromatin immunoprecipitation analysis showed that FoxO1 bound to the p21/p27 promoter DNA, indicating that FoxO1 suppresses cell proliferation through these factors. In addition, FoxO1 induced the expression of ectodysplasin A (Eda) and its receptor Eda2r, which are known to be associated with X-linked hypohidrotic ectodermal dysplasia and are involved in salivary gland development in myoepithelial cells. FoxO1 inhibitors suppressed Eda/Eda2r expression and salivary gland development in primordial organ cultures after mesenchymal removal. Although mesenchymal cells are considered a source of Eda, myoepithelial cells might be one of the resources of Eda. These results suggest that FoxO1 regulates myoepithelial cell proliferation and Eda secretion during salivary gland development in myoepithelial cells.