Iwama Hideaki, Mehanna Sally, Imasaka Mai, Hashidume Shinsuke, Nishiura Hiroshi, Yamamura Ken-Ichi, Suzuki Chigure, Uchiyama Yasuo, Hatano Etsuro, Ohmuraya Masaki
Department of Genetics, Hyogo College of Medicine, 1-1, Mukogawa-cho, Nishinomiya, Hyogo, 663-8501, Japan.
Department of Gastroenterological Surgery, Hyogo College of Medicine, Nishinomiya, Hyogo, 663-8501, Japan.
Sci Rep. 2021 Mar 23;11(1):6596. doi: 10.1038/s41598-021-85898-9.
The major lysosomal proteases, Cathepsin B (CTSB), Cathepsin D (CTSD) and Cathepsin L (CTSL), are implicated in autophagic activity. To investigate the role of each cathepsin in the exocrine pancreas, we generated mice in which the pancreas was specifically deficient in Ctsb, Ctsd and Ctsl. Each of these gene knockout (KO) and Ctsb;Ctsl and Ctsd;Ctsl double-knockout (DKO) mice were almost normal. However, we found cytoplasmic degeneration in the pancreatic acinar cells of Ctsb;Ctsd DKO mice, similar to autophagy related 5 (Atg5) KO mice. LC3 and p62 (autophagy markers) showed remarkable accumulation and the numbers of autophagosomes and autolysosomes were increased in the pancreatic acinar cells of Ctsb;Ctsd DKO mice. Moreover, these Ctsb;Ctsd DKO mice also developed chronic pancreatitis (CP). Thus, we conclude that both Ctsb and Ctsd deficiency caused impaired autophagy in the pancreatic acinar cells, and induced CP in mice.
主要的溶酶体蛋白酶,组织蛋白酶B(CTSB)、组织蛋白酶D(CTSD)和组织蛋白酶L(CTSL),与自噬活性有关。为了研究每种组织蛋白酶在外分泌胰腺中的作用,我们构建了胰腺特异性缺乏Ctsb、Ctsd和Ctsl的小鼠。这些基因敲除(KO)小鼠以及Ctsb;Ctsl和Ctsd;Ctsl双敲除(DKO)小鼠几乎都是正常的。然而,我们在Ctsb;Ctsd DKO小鼠的胰腺腺泡细胞中发现了细胞质变性,这与自噬相关5(Atg5)KO小鼠相似。LC3和p62(自噬标志物)在Ctsb;Ctsd DKO小鼠的胰腺腺泡细胞中显示出显著积累,并且自噬体和自溶酶体的数量增加。此外,这些Ctsb;Ctsd DKO小鼠还发生了慢性胰腺炎(CP)。因此,我们得出结论,Ctsb和Ctsd的缺乏均导致胰腺腺泡细胞自噬受损,并在小鼠中诱发了CP。