Suppr超能文献

高质量重症联合免疫缺陷(SCID)大鼠生物资源。

A high-quality severe combined immunodeficiency (SCID) rat bioresource.

机构信息

Institute of Experimental Animal Sciences, Graduate School of Medicine, Osaka University, Suita City, Osaka, Japan.

Division of Animal Genetics, Laboratory Animal Research Center, Institute of Medical Science, The University of Tokyo, Minato-ku, Tokyo, Japan.

出版信息

PLoS One. 2022 Aug 12;17(8):e0272950. doi: 10.1371/journal.pone.0272950. eCollection 2022.

Abstract

Immunodeficient animals are valuable models for the engraftment of exogenous tissues; they are widely used in many fields, including the creation of humanized animal models, as well as regenerative medicine and oncology. Compared with mice, laboratory rats have a larger body size and can more easily undergo transplantation of various tissues and organs. Considering the absence of high-quality resources of immunodeficient rats, we used the CRISPR/Cas9 genome editing system to knock out the interleukin-2 receptor gamma chain gene (Il2rg) in F344/Jcl rats-alone or together with recombination activating gene 2 (Rag2)-to create a high-quality bioresource that researchers can freely use: severe combined immunodeficiency (SCID) rats. We selected one founder rat with frame-shift mutations in both Il2rg (5-bp del) and Rag2 ([1-bp del+2-bp ins]/[7-bp del+2-bp ins]), then conducted mating to establish a line of immunodeficient rats. The immunodeficiency phenotype was preliminarily confirmed by the presence of severe thymic hypoplasia in Il2rg-single knockout (sKO) and Il2rg/Rag2-double knockout (dKO) rats. Assessment of blood cell counts in peripheral blood showed that the white blood cell count was significantly decreased in sKO and dKO rats, while the red blood cell count was unaffected. The decrease in white blood cell count was mainly caused by a decrease in lymphocytes. Furthermore, analyses of lymphocyte populations via flow cytometry showed that the numbers of B cells (CD3- CD45+) and natural killer cells (CD3- CD161+) were markedly reduced in both knockout rats. In contrast, T cells were markedly reduced but showed slightly different results between sKO and dKO rats. Notably, our immunodeficient rats do not exhibit growth retardation or gametogenesis defects. This high-quality SCID rat resource is now managed by the National BioResource Project in Japan. Our SCID rat model has been used in various research fields, demonstrating its importance as a bioresource.

摘要

免疫缺陷动物是异种组织移植的有价值模型;它们被广泛应用于许多领域,包括人类化动物模型的创建、再生医学和肿瘤学。与小鼠相比,实验大鼠体型较大,更容易进行各种组织和器官的移植。考虑到缺乏高质量的免疫缺陷大鼠资源,我们使用 CRISPR/Cas9 基因组编辑系统敲除 F344/Jcl 大鼠的白细胞介素 2 受体γ链基因(Il2rg)-单独或与重组激活基因 2(Rag2)一起-创建了一种高质量的生物资源,研究人员可以自由使用:严重联合免疫缺陷(SCID)大鼠。我们选择了一只 Il2rg(5-bp del)和 Rag2([1-bp del+2-bp ins]/[7-bp del+2-bp ins])都有移码突变的创始大鼠,然后进行交配建立免疫缺陷大鼠系。Il2rg 单敲除(sKO)和 Il2rg/Rag2 双敲除(dKO)大鼠严重胸腺发育不全的存在初步证实了免疫缺陷表型。外周血血细胞计数评估显示,sKO 和 dKO 大鼠的白细胞计数显著下降,而红细胞计数不受影响。白细胞计数的下降主要是由于淋巴细胞减少。此外,通过流式细胞术分析淋巴细胞群显示,两种敲除大鼠的 B 细胞(CD3- CD45+)和自然杀伤细胞(CD3- CD161+)数量明显减少。相反,T 细胞明显减少,但 sKO 和 dKO 大鼠之间的结果略有不同。值得注意的是,我们的免疫缺陷大鼠没有表现出生长迟缓或配子发生缺陷。这种高质量的 SCID 大鼠资源现在由日本国家生物资源项目管理。我们的 SCID 大鼠模型已被用于各种研究领域,证明了其作为生物资源的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b50/9374221/133b4099dfd7/pone.0272950.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验