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隐性错义 LAMP3 变异与犬层状小体生物发生缺陷和致命性新生儿间质性肺病有关。

Recessive missense LAMP3 variant associated with defect in lamellar body biogenesis and fatal neonatal interstitial lung disease in dogs.

机构信息

Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland.

Department of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland.

出版信息

PLoS Genet. 2020 Mar 9;16(3):e1008651. doi: 10.1371/journal.pgen.1008651. eCollection 2020 Mar.

DOI:10.1371/journal.pgen.1008651
PMID:32150563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7082050/
Abstract

Neonatal interstitial lung diseases due to abnormal surfactant biogenesis are rare in humans and have never been reported as a spontaneous disorder in animals. We describe here a novel lung disorder in Airedale Terrier (AT) dogs with clinical symptoms and pathology similar to the most severe neonatal forms of human surfactant deficiency. Lethal hypoxic respiratory distress and failure occurred within the first days or weeks of life in the affected puppies. Transmission electron microscopy of the affected lungs revealed maturation arrest in the formation of lamellar bodies (LBs) in the alveolar epithelial type II (AECII) cells. The secretory organelles were small and contained fewer lamellae, often in combination with small vesicles surrounded by an occasionally disrupted common limiting membrane. A combined approach of genome-wide association study and whole exome sequencing identified a recessive variant, c.1159G>A, p.(E387K), in LAMP3, a limiting membrane protein of the cytoplasmic surfactant organelles in AECII cells. The substitution resides in the LAMP domain adjacent to a conserved disulfide bond. In summary, this study describes a novel interstitial lung disease in dogs, identifies a new candidate gene for human surfactant dysfunction and brings important insights into the essential role of LAMP3 in the process of the LB formation.

摘要

由于表面活性物质生物发生异常导致的新生儿间质性肺疾病在人类中很少见,在动物中也从未报道过自发性疾病。我们在这里描述了一种新型的艾尔谷梗犬(Airedale Terrier,AT)肺部疾病,其临床症状和病理学与人类最严重的新生儿型表面活性物质缺乏症相似。受影响的幼犬在生命的最初几天或几周内出现致命性低氧性呼吸窘迫和衰竭。受影响肺部的透射电子显微镜显示,肺泡上皮细胞 II 型(alveolar epithelial type II,AECII)中板层小体(lamellar body,LB)的形成出现成熟停滞。分泌细胞器较小,所含板层较少,通常与小泡结合,小泡周围偶尔有不连续的常见限膜。全基因组关联研究和全外显子组测序的综合方法确定了 LAMP3 中的一个隐性变异 c.1159G>A,p.(E387K),这是 AECII 细胞中细胞质表面活性物质细胞器的限膜蛋白。该取代位于与保守二硫键相邻的 LAMP 结构域内。总之,本研究描述了一种新型的犬间质性肺病,确定了人类表面活性物质功能障碍的一个新候选基因,并为 LAMP3 在 LB 形成过程中的重要作用提供了重要见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8da/7082050/6485d80204de/pgen.1008651.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8da/7082050/1f0f14665c19/pgen.1008651.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8da/7082050/f081479f860e/pgen.1008651.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8da/7082050/3ccf264c8029/pgen.1008651.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8da/7082050/6485d80204de/pgen.1008651.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8da/7082050/1f0f14665c19/pgen.1008651.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8da/7082050/f081479f860e/pgen.1008651.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8da/7082050/3ccf264c8029/pgen.1008651.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8da/7082050/6485d80204de/pgen.1008651.g006.jpg

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Hum Genet. 2019 Dec;138(11-12):1301-1311. doi: 10.1007/s00439-019-02073-x. Epub 2019 Nov 4.
3
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