Identification of TEKTIN1‐expressing multiciliated cells during spontaneous differentiation of non‐human primate embryonic stem cells

Author:

Nishie Tomomi1,Ohta Yoshio1,Shirai Emi1,Higaki Shogo1,Shimozawa Nobuhiro2,Narita Keishi3,Kawaguchi Kotoku4,Tanaka Hideyuki5,Mori Chika1,Tanaka Taiga1,Hirabayashi Masumi6,Suemori Hirofumi7,Kurisaki Akira8,Tooyama Ikuo9,Asano Shinji4,Takeda Sén35,Takada Tatsuyuki1ORCID

Affiliation:

1. Laboratory of Cell Engineering, Department of Pharmaceutical Sciences Ritsumeikan University Kusatsu Shiga Japan

2. Tsukuba Primate Research Center, National Institutes of Biomedical Innovation Health and Nutrition Tsukuba‐shi Ibaraki Japan

3. Department of Anatomy and Cell Biology, Interdisciplinary Graduate School University of Yamanashi Chuo Yamanashi Japan

4. Department of Molecular Physiology, College of Pharmaceutical Sciences Ritsumeikan University Kusatsu Shiga Japan

5. Department of Anatomy Teikyo University School of Medicine Itabashi Tokyo Japan

6. Center for Genetic Analysis of Behavior National Institute for Physiological Sciences Okazaki Aichi Japan

7. Center for Human ES Cell Research, Institute for Frontier Life and Medical Sciences Kyoto University Kyoto Japan

8. Graduate School of Biological Sciences Nara Institute of Science and Technology Nara Japan

9. Molecular Neuroscience Research Center and Medical Innovation Research Center Shiga University of Medical Science Shiga Japan

Abstract

AbstractTektins are a group of microtubule‐stabilizing proteins necessary for cilia and flagella assembly. TEKTIN1 (TEKT1) is used as a sperm marker for monitoring germ cell differentiation in embryonic stem (ES) and induced pluripotent stem (iPS) cells. Although upregulation of TEKT1 has been reported during spontaneous differentiation of ES and iPS cells, it is unclear which cells express TEKT1. To identify TEKT1‐expressing cells, we established an ES cell line derived from cynomolgus monkeys (Macaca fascicularis), which expresses Venus controlled by the TEKT1 promoter. Venus expression was detected at 5 weeks of differentiation on the surface of the embryoid body (EB), and it gradually increased with the concomitant formation of a leash‐like structure at the EB periphery. Motile cilia were observed on the surface of the Venus‐positive leash‐like structure after 8 weeks of differentiation. The expression of cilia markers as well as TEKT1–5 and 9 + 2 microtubule structures, which are characteristic of motile cilia, were detected in Venus‐positive cells. These results demonstrated that TEKT1‐expressing cells are multiciliated epithelial‐like cells that form a leash‐like structure during the spontaneous differentiation of ES and iPS cells. These findings will provide a new research strategy for studying cilia biology, including ciliogenesis and ciliopathies.

Funder

Japan Science and Technology Agency

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Wiley

Subject

Cell Biology,Genetics

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