The C-type lectin family with the signature C-type lectin-like domain promotes antibacterial host defense within the animal kingdom. We examined the role of Chinese mitten crab, (H. Milne-Edwards) (Decapoda: Grapsidae) Ig domain-containing C-type lectin (IgLectin), a novel and poorly understood member of the C-type lectin family. was expressed primarily by both hemocytes ( ) and intestines, with significantly induced mRNA expression on intestinal or hemolymph bacterial infections. As a soluble protein, both its C-type lectin-like domain and the Ig domain were required for bacterial binding, bacterial agglutination, bacterial growth inhibition, and in vivo bacterial clearance. Polymeric IgLectin could be const... More
The C-type lectin family with the signature C-type lectin-like domain promotes antibacterial host defense within the animal kingdom. We examined the role of Chinese mitten crab, (H. Milne-Edwards) (Decapoda: Grapsidae) Ig domain-containing C-type lectin (IgLectin), a novel and poorly understood member of the C-type lectin family. was expressed primarily by both hemocytes ( ) and intestines, with significantly induced mRNA expression on intestinal or hemolymph bacterial infections. As a soluble protein, both its C-type lectin-like domain and the Ig domain were required for bacterial binding, bacterial agglutination, bacterial growth inhibition, and in vivo bacterial clearance. Polymeric IgLectin could be constructed via the disulfide bond in the Ig domain, significantly enhancing IgLectin antibacterial activity. IgLectin promoted bacterial phagocytosis in an Ig domain-dependent manner in hemocytes, while it controlled microbial homeostasis and protected against bacteria-induced inflammation in the intestine. Protein interaction studies revealed that the IgLectin Ig domain bound to the first Ig domain of the polymeric Ig receptor, which was essential for IgLectin-induced bacterial phagocytosis. The temporal sequence of cell interactions during intestinal inflammation is only beginning to be understood. In this article, we show that hemocyte-derived IgLectin entered the intestinal wall at the later phase of intestinal inflammation. Moreover, IgLectin protected the host against intestinal and hemolymph infections in a polymeric Ig receptor-dependent manner. Therefore, the IgLectin promoted bacterial clearance and protected against inflammatory disease through an independent or synergistic effect of hemocytes and intestines in invertebrates.
