ヒト サイハツ シンケイ コウシュ デノ ダイ10 センショクタイ ケッシツ ノ チクセキ ト ソノ イギ

K, Tokiyoshi; T, Yoshiminc; M, Maruno; AKMG, Muhammad; T, Hayakawa. Accumulation of allelic losses on chromosome 10 in human gliomas at recurrence. Journal of clinical pathology. 1996. 49(4), M218-M222

Bactericidal Activity of Mouse α-Defensin, Cryptdin-4 Predominantly Affects Noncommensal Bacteria

Mouse Paneth cell α-defensins, termed cryptdins, are secreted into the intestinal lumen, exert microbicidal activity and contribute to intestinal innate immunity. Among them, cryptdin-4 (Crp4) has the most potent microbicidal activity. In the intestinal lumen, commensal bacteria colonize and elicit beneficial effects to the host. However, the effects of Crp4 against commensal bacteria are poorly understood. Thus, we investigated the bactericidal activities of Crp4 against commensal bacteria compared to non-commensal bacteria. Oxidized Crp4 showed only minimal or no bactericidal activity against 8 out of 12 commensal bacterial species, including Bifidobacterium bifidum and Lactobacillus Casei. We further addressed a role of the conserved disulfide bonds of Crp4 by analyzing reduced Crp4 (r-Crp4). r-Crp4 demonstrated significantly greater bactericidal activities against 7 of 12 commensal bacteria than did oxidized Crp4. Oxidized Crp4 and r-Crp4 elicited equivalently potent bactericidal activities against 11 of 11 non-commensal bacteria tested such as Salmonella enterica serovar Typhimurium, and 5 of 12 commensal bacteria. Furthermore, when r-Crp4 was exposed to a processing enzyme of cryptdins, MMP-7, r-Crp4 was degraded and bactericidal activities disappeared. These findings suggest that Crp4 has selective bactericidal activities against intestinal microbiota and that the activities are dependent on the disulfide bonds