CD9-positive cells in the intermediate lobe migrate into the anterior lobe to supply endocrine cells

• Published in: Histochemistry and cell biology 2021-10, Vol.156 (4), p.301-313
• Main Authors: Horiguchi, K., Fujiwara, K., Tsukada, T., Nakakura, T., Yoshida, S., Hasegawa, R., Takigami, S., Ohsako, S.
• Format: Article
• Language: English
• Subjects: Animals; Biochemistry; Biomedical and Life Sciences; Biomedicine; CD81 antigen; CD9 antigen; Cell adhesion & migration; Cell Biology; Cell culture; Cell migration; Cell Movement; Developmental Biology; DNA microarrays; Endocrine Cells - metabolism; Male; Mesenchyme; Original Paper; Pituitary; Pituitary (anterior); Pituitary Gland, Anterior - metabolism; Progenitor cells; Rats; Rats, Wistar; Scanning electron microscopy; siRNA; Snail protein; Stem cells; Tetraspanin 29 - metabolism; Tissue culture; Transcription
• ISSN: 0948-6143; 1432-119X
• DOI: 10.1007/s00418-021-02009-5

The adenohypophysis is composed of the anterior and intermediate lobes (AL and IL), and secretes important hormones for growth, sexual development, metabolism, and reproduction. In the marginal cell layer (MCL) facing Rathke’s cleft between the IL and AL, cluster of differentiation (CD) 9-, CD81-, S100β-, and SOX2-quadruple positive (CD9/CD81/S100β/SOX2-positive) cells in the adult IL are settled as tissue-resident stem/progenitor cells supplying hormone-producing cells to the AL. However, it is unclear how CD9/CD81/S100β/SOX2-positive cells in the IL-side MCL migrate into the AL across Rathke’s cleft. In the present study, we performed chimeric pituitary tissue culture using S100β/GFP-transgenic rats and Wistar rats, and traced the footprint of S100β/GFP-expressing cells. We detected IL-side S100β/GFP-expressing cells in the AL tissue, demonstrating that these cells migrate from the IL to the AL. However, the cells failed to migrate in the opposite direction. Consistently, scanning electron microscopic analysis revealed well-developed cytoplasmic protrusions in the IL-side MCL, but not in the AL-side MCL, suggesting that IL-side CD9/CD81/S100β/SOX2-positive cells had higher migratory activity. We also searched for a specific marker for IL-side CD9/CD81/S100β/SOX2-positive cells and identified tetraspanin 1 (TSPAN1) from microarray analysis. Downregulation of Tspan1 by specific siRNA impaired cell migration and significantly reduced expression of snail family transcriptional repressor 2 ( Slug ), a marker of epithelial-mesenchymal transition (EMT). Therefore, CD9/CD81/S100β/SOX2-positive cells in the IL-side MCL can be stem/progenitor cells that provide stem/progenitor cells to the AL-side MCL via SLUG-mediated EMT and cell migration.