Characterization of cultivated murine lacrimal gland epithelial cells

Shinya Kobayashi, Tetsuya Kawakita, Motoko Kawashima, Naoko Okada, Kenji Mishima, Ichiro Saito, Masataka Ito, Shigeto Shimmura, Kazuo Tsubota

研究成果: Article査読

16 被引用数 (Scopus)

抄録

Purpose: To date, mouse lacrimal gland epithelial cells have been cultured successfully but only in cases involving newborn mouse lacrimal glands. In this work, we attempted to cultivate and characterize adult mouse lacrimal gland epithelial cells. Methods: Lacrimal glands were removed from newborn mice (C57B/6) and isolated lacrimal gland epithelial cells were seeded onto tissue culture treated or low adherent culture dishes in Cnt-07 culture medium with or without cholera toxin. Cultivated cells were characterized by immunostaining with pan-cytokeratin, α-smooth muscle actin, and lactoferrin antibodies. Lacrimal gland cells from 7-week-old green fluorescent protein (GFP) and non-GFP (C57B/6) mice were mixed and seeded onto uncoated dishes to assess sphere-forming efficiency. Cells were also seeded onto 3T3 cell feeder layers to assess colony forming efficiency. Results: Lacrimal gland epithelial cells were selectively cultured with cholera toxin, and cell type was verified by pancytokeratin and α-smooth muscle actin immunostaining. Sphere formation from single cells of adult mice was observed using specific medium and low adherent culture dishes. These cells could also undergo colony formation on 3T3 feeder cells. Conclusions: Adult mouse lacrimal gland epithelial cells were successfully cultivated in cholera toxin-containing medium, and were observed to form spheres from single cells.

本文言語English
ページ(範囲)1271-1277
ページ数7
ジャーナルMolecular vision
18
出版ステータスPublished - 2012 5月 12

ASJC Scopus subject areas

  • 眼科学

フィンガープリント

「Characterization of cultivated murine lacrimal gland epithelial cells」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル