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Article Abstract

Serine proteases are widely distributed in both invertebrates and vertebrates, playing critical roles in the regulation of innate immunity. In the insect innate immune system, two pivotal pathways-the prophenoloxidase (PPO) activation cascade and Toll pathway-mediated antimicrobial peptide (AMP) synthesis-are both tightly regulated by serine protease cascades. This study focuses on serine protease-hemolymph protease 6 of (-HP6). Following immune stimulation, the expression of -proHP6 was significantly induced, primarily observed in hemocytes and the fat body. After suppressing -proHP6 expression via RNA interference (RNAi) and infecting larvae with different microbes, the expression levels of AMPs showed a downward trend. When endogenous -proHP6 content in hemolymph was reduced using RNAi technology or anti-r-proHP6-His polyclonal antibodies, PAMPs/microbe-mediated phenoloxidase (PO) activity significantly decreased. These results suggest that -HP6 has a positive regulatory effect on PPO activation and AMP synthesis. Additionally, the in vitro hydrolysis of r-proHP6-Tb-His yielded r-HP6 with serine protease activity, which exhibited optimal reaction conditions for S-2288 at pH 8.0, 50 °C, and 15 min.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12111086PMC
http://dx.doi.org/10.3390/ijms26104514DOI Listing

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