Journal Article

Generation of heterozygous PKD1 mutant pigs exhibiting early-onset renal cyst formation

Nagaya, Masaki, Nakauchi, Hiromitsu, Okamoto, Kazutoshi, Umeyama, Kazuhiro, Uchikura, Ayuko, Nagashima, Hiroshi, Hasegawa, Koki, Fukuda, Toru, Yamanaka, Shuichiro, Yokoo, Takashi, Tajiri, Susumu, Nakano, Kazuaki, Matsumoto, Kei, Watanabe, Masahito, Takayanagi, Shuko, Matsunari, Hitomi

2022

Overview

Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited kidney disease, manifesting as the progressive development of fluid-filled renal cysts. In approximately half of all patients with ADPKD, end-stage renal disease results in decreased renal function. In this study, we used CRISPR-Cas9 and somatic cell cloning to produce pigs with the unique mutation c.152_153insG (PKD1insG/+). Pathological analysis of founder cloned animals and progeny revealed that PKD1insG/+ pigs developed many pathological conditions similar to those of patients with heterozygous mutations in PKD1. Pathological similarities included the formation of macroscopic renal cysts at the neonatal stage, number and cystogenic dynamics of the renal cysts formed, interstitial fibrosis of the renal tissue, and presence of a premature asymptomatic stage. Our findings demonstrate that PKD1insG/+ pigs recapitulate the characteristic symptoms of ADPKD. Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disorder characterized by the formation of cysts within the kidneys. The authors generated PKD1 heterozygous knockout (PKD1insG/+) pigs by CRISPR-Cas9 and somatic cell cloning techniques. The founder cloned animals and progeny showed the renal cyst formation from the neonatal stage, interstitial fibrosis of the renal tissue, and the presence of a premature asymptomatic stage. Their findings demonstrate that PKD1insG/+ pigs recapitulate the characteristic symptoms of ADPKD.

• Publisher: Elsevier Inc,Nature Publishing Group US,Nature Publishing Group
• Subject: 13/109 / 45/23 / 45/41 / 45/90 / 64 / 692/308/1426 / 692/699/1585/104/1586 / 82/51 / Age / Animals / Asymptomatic / Cloning / CRISPR / Cysts / End-stage renal disease / Female / Fibrosis / Genetic disorders / Heterozygote / Humans / Kidney - pathology / Kidney diseases / Kidneys / Laboratory Medicine / Male / Medicine / Medicine & Public Health / Mutation / Neonates / Offspring / Pathology / Polycystic kidney / Polycystic Kidney, Autosomal Dominant - genetics / Polycystic Kidney, Autosomal Dominant - pathology / Progeny / Renal function / Signs and symptoms / Swine / technical-report / TRPP Cation Channels - genetics