Paneth Cell Secretion in vivo Requires Expression of Tmem16a and Tmem16f

Rainer Schreiber; Ines Cabrita; Karl Kunzelmann

doi:10.1016/j.gastha.2022.08.002

Paneth Cell Secretion in vivo Requires Expression of Tmem16a and Tmem16f

Gastro Hep Adv. 2022 Aug 7;1(6):1088-1098. doi: 10.1016/j.gastha.2022.08.002. eCollection 2022.

Authors

Rainer Schreiber¹, Ines Cabrita², Karl Kunzelmann¹

Affiliations

¹ Institut für Physiologie, Universität Regensburg, Regensburg, Bavaria, Germany.
² Nephrologisches Forschungslabor, University of Cologne, Köln, NRW, Germany.

Abstract

Background and aims: Paneth cells play a central role in intestinal innate immune response. These cells are localized at the base of small intestinal crypts of Lieberkuhn. The calcium-activated chloride channel TMEM16A and the phospholipid scramblase TMEM16F control intracellular Ca²⁺ signaling and exocytosis. We analyzed the role of TMEM16A and TMEM16F for Paneth cells secretion.

Methods: Mice with intestinal epithelial knockout of Tmem16a (Tmem16a^-/-) and Tmem16f (Tmem16f^-/-) were generated. Tissue structures and Paneth cells were analyzed, and Paneth cell exocytosis was examined in small intestinal organoids in vitro. Intracellular Ca²⁺ signals were measured and were compared between wild-type and Tmem16 knockout mice. Bacterial colonization and intestinal apoptosis were analyzed.

Results: Paneth cells in the crypts of Lieberkuhn from Tmem16a^-/- and Tmem16f^-/- mice demonstrated accumulation of lysozyme. Tmem16a and Tmem16f were localized in wild-type Paneth cells but were absent in cells from knockout animals. Paneth cell number and size were enhanced in the crypt base and mucus accumulated in intestinal goblet cells of knockout animals. Granule fusion and exocytosis on cholinergic and purinergic stimulation were examined online. Both were strongly compromised in the absence of Tmem16a or Tmem16f and were also blocked by inhibition of Tmem16a/f. Purinergic Ca²⁺ signaling was largely inhibited in Tmem16a knockout mice. Jejunal bacterial content was enhanced in knockout mice, whereas cellular apoptosis was inhibited.

Conclusion: The present data demonstrate the role of Tmem16 for exocytosis in Paneth cells. Inhibition or activation of Tmem16a/f is likely to affect microbial content and immune functions present in the small intestine.

Keywords: ANO1; ANO6; Anoctamin 1; Anoctamin 6; Ca2+-Activated Cl− Channel; Exocytosis; Goblet Cells; Paneth Cells; Phospholipid Scrambling; Secretion; TMEM16A; TMEM16F.