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IFT140<sup>+</sup>/K14<sup>+</sup> cells function as stem/progenitor cells in salivary glands.

Xue-Ming ZhangJi ZhouXinyu WangJiangyu GengYubei ChenYao Sun
Published in: International journal of oral science (2022)
Stem/progenitor cells are important for salivary gland development, homeostasis maintenance, and regeneration following injury. Keratin-14<sup>+</sup> (K14<sup>+</sup>) cells have been recognized as bona fide salivary gland stem/progenitor cells. However, K14 is also expressed in terminally differentiated myoepithelial cells; therefore, more accurate molecular markers for identifying salivary stem/progenitor cells are required. The intraflagellar transport (IFT) protein IFT140 is a core component of the IFT system that functions in signaling transduction through the primary cilia. It is reportedly expressed in mesenchymal stem cells and plays a role in bone formation. In this study, we demonstrated that IFT140 was intensively expressed in K14<sup>+</sup> stem/progenitor cells during the developmental period and early regeneration stage following ligation-induced injuries in murine submandibular glands. In addition, we demonstrated that IFT140<sup>+</sup>/ K14<sup>+</sup> could self-renew and differentiate into granular duct cells at the developmental stage in vivo. The conditional deletion of Ift140 from K14<sup>+</sup> cells caused abnormal epithelial structure and function during salivary gland development and inhibited regeneration. IFT140 partly coordinated the function of K14<sup>+</sup> stem/progenitor cells by modulating ciliary membrane trafficking. Our investigation identified a combined marker, IFT140<sup>+</sup>/K14<sup>+</sup>, for salivary gland stem/progenitor cells and elucidated the essential role of IFT140 and cilia in regulating salivary stem/progenitor cell differentiation and gland regeneration.
Keyphrases
  • induced apoptosis
  • cell cycle arrest
  • mesenchymal stem cells
  • endoplasmic reticulum stress
  • cell death
  • bone marrow
  • cell proliferation
  • endothelial cells
  • single molecule
  • cell therapy
  • diabetic rats