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Sublingual immune cell clusters and dendritic cell distribution in the oral cavity
Yutaka Kusumoto, Mizuki Ueda, Mayuko Hashimoto, Haruka Takeuchi, Naoko Okada, Junya Yamamoto, Akiko Nishii, Atsuki Fujino, Akiho Kurahashi, Momoka Satoh, Yuki Iwasa, Koki Okamura, Karin Obazaki, Ryoto Kumagai, Naruya Sakamoto, Yuto Tanaka, Yukika Kamiya, Tetsushi Hoshida, Tsuneyasu Kaisho, Hiroaki Hemmi, Tomoya Katakai, Tetsuya Honda, Junichi Kikuta, Kosuke Kataoka, Ryoyo Ikebuchi, Taiki Moriya, Takahiro Adachi, Takeshi Watanabe, Masaru Ishii, Atsushi Miyawaki, Kenji Kabashima, Tatyana Chtanova, Michio Tomura
Yutaka Kusumoto, Mizuki Ueda, Mayuko Hashimoto, Haruka Takeuchi, Naoko Okada, Junya Yamamoto, Akiko Nishii, Atsuki Fujino, Akiho Kurahashi, Momoka Satoh, Yuki Iwasa, Koki Okamura, Karin Obazaki, Ryoto Kumagai, Naruya Sakamoto, Yuto Tanaka, Yukika Kamiya, Tetsushi Hoshida, Tsuneyasu Kaisho, Hiroaki Hemmi, Tomoya Katakai, Tetsuya Honda, Junichi Kikuta, Kosuke Kataoka, Ryoyo Ikebuchi, Taiki Moriya, Takahiro Adachi, Takeshi Watanabe, Masaru Ishii, Atsushi Miyawaki, Kenji Kabashima, Tatyana Chtanova, Michio Tomura
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Research Article Immunology

Sublingual immune cell clusters and dendritic cell distribution in the oral cavity

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Abstract

The oral mucosa is the first line of defense against pathogenic bacteria and plays a vital role in maintaining tolerance to food antigens and commensal bacteria. We used CD11c reporter mice to visualize dendritic cells (DCs), a key immune cell population, in the oral cavity. We identified differences in DC density in each oral tissue region. Sublingual immune cell clusters (SLICs) extended from the lamina propria to the epithelium, where DCs and T cells resided in close contact with each other and innate lymphoid cells. Targeted in situ photolabeling revealed that the SLICs comprised mostly CD11c+CD11b+ DCs and were enriched for cDC1s and Langerhans cells. Although the frequency of T cell subsets was similar within and outside the SLICs, tissue-resident memory T cells were significantly enriched within the clusters and cluster size increased in response to inflammation. Collectively, we found that SLICs form a unique microenvironment that facilitates T cell–DC interactions in the steady state and during inflammation. Since the oral mucosa is an important target for needle-free vaccination and sublingual immunotherapy to induce tolerogenic responses, the insight into the localized immunoregulation provided in this study may accelerate the development of these approaches.

Authors

Yutaka Kusumoto, Mizuki Ueda, Mayuko Hashimoto, Haruka Takeuchi, Naoko Okada, Junya Yamamoto, Akiko Nishii, Atsuki Fujino, Akiho Kurahashi, Momoka Satoh, Yuki Iwasa, Koki Okamura, Karin Obazaki, Ryoto Kumagai, Naruya Sakamoto, Yuto Tanaka, Yukika Kamiya, Tetsushi Hoshida, Tsuneyasu Kaisho, Hiroaki Hemmi, Tomoya Katakai, Tetsuya Honda, Junichi Kikuta, Kosuke Kataoka, Ryoyo Ikebuchi, Taiki Moriya, Takahiro Adachi, Takeshi Watanabe, Masaru Ishii, Atsushi Miyawaki, Kenji Kabashima, Tatyana Chtanova, Michio Tomura

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Figure 4

Single DCs and DC clusters in the posterior region of the sublingual mucosa.

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Single DCs and DC clusters in the posterior region of the sublingual muc...
(A) Image of the entire tissue-cleared tongue of CD11c-YFP mouse acquired using a light-sheet microscope (orange signal is autofluorescence of surface of tongue). (B) Bright-field (left panel) and fluorescence (right panel) images of the sublingual mucosa of CD11c-YFP mouse. Fluorescence images of the anterior (red square), middle (light-blue square), and posterior (blue square) regions of the sublingual surface. (C and D) Numbers of single DCs and DC clusters in the 3 subdivided regions in B. Data represent mean ± SD, single DCs (n = 18), DC clusters (n = 8). Statistical comparisons were performed using 1-way ANOVA with Tukey’s multiple-comparison test. **P < 0.01; ***P < 0.001; ****P < 0.0001. (E–I) Images of tissue-cleared sublingual mucosa of CD11c-YFP mice were acquired using confocal microscopy. Sublingual mucosa (E and F), DCs in the epithelium (G) (Supplemental Video 2), single DCs (H), and a DC cluster (I) (Supplemental Video 3) in the LP. (J and K) Fluorescence images of DCs in the sublingual posterior region in Langerin-Cre/KikGR mice. The white square in J was further magnified and shown in K. (L) Fluorescence image of the coronally cut surface of the sublingual tongue. Green, CD11c-YFP. Red, autofluorescence. Blue, DAPI. The data are representative of at least 3 independent experiments. Scale bars: 50 μm (B and E–K) and 25 μm (L). Mus, muscle layer; LP, lamina propria; Ep, epithelium.

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