Suppr超能文献

Il2rg、Rag2或Il2rg/Rag2双敲除大鼠的免疫缺陷表型;人白血病异种移植模型的建立。

Immune deficiency phenotypes of Il2rg, Rag2 or Il2rg/Rag2 double knockout rats; establishment of human leukemia xenograft models.

作者信息

Kim Joo-Il, Lim Hyun-Jin, Kwon Euna, Mashimo Tomoji, Kang Byeong-Cheol

机构信息

Department of Experimental Animal Research, Biomedical Research Institute, Seoul National Univ. Hospital, Seoul, Korea.

Graduate School of Translational Medicine, Seoul National University College of Medicine, 101 Daehak-ro, Jongno-gu, Seoul, 03080, Republic of Korea.

出版信息

Lab Anim Res. 2024 Dec 27;40(1):43. doi: 10.1186/s42826-024-00231-5.

Abstract

BACKGROUND

Genetically immunodeficient mice lacking Il2rg and Rag2 genes have been widely utilized in the field of biomedical research. However, immunodeficient rats, which offer the advantage of larger size, have not been as extensively used to date. Recently, Severe Combined Immunodeficiency (SCID) rats were generated using CRISPR/Cas9 system, targeting Il2rg and Rag2 in National BioResource Project in Japan. We imported and investigated more detailed phenotypes of wild-type (WT) Il2rg knockout (KO), Rag2 KO and Il2rg/Rag2 KO rats for 20 weeks.

RESULTS

During experiments, Il2rg KO, Rag2 KO and Il2rg/Rag2 KO rats showed decreased white blood cells and systemic lymphopenia, with reduced CD4+, CD8+ T cells and CD161+ NK cells. Additionally, all KO strains exhibited reduced relative spleen weights, hypoplasia of the germinal center in the white pulp, and atrophy with the disappearance of the boundary between the cortex and medulla in the thymus, compared to WT rats. Furthermore, we established human acute lymphoblastic leukemia xenograft rat model by intravenously injecting 5.0 × 10 cells/kg of NALM6 cells into Il2rg/Rag2 KO rats.

CONCLUSIONS

These findings indicate that Il2rg KO, Rag2 KO, and Il2rg/Rag2 KO rats exhibited SCID phenotypes, suggesting their potential application as immunodeficient animal models for tumor xenograft studies.

摘要

背景

缺乏Il2rg和Rag2基因的基因免疫缺陷小鼠已在生物医学研究领域中广泛应用。然而,具有体型较大优势的免疫缺陷大鼠迄今为止尚未得到如此广泛的应用。最近,日本国家生物资源项目利用CRISPR/Cas9系统,通过靶向Il2rg和Rag2基因培育出了严重联合免疫缺陷(SCID)大鼠。我们引进了野生型(WT)Il2rg基因敲除(KO)、Rag2基因敲除和Il2rg/Rag2基因敲除大鼠,并对其进行了为期20周的更详细表型研究。

结果

在实验过程中,Il2rg基因敲除、Rag2基因敲除和Il2rg/Rag2基因敲除大鼠的白细胞减少,出现全身性淋巴细胞减少,CD4 +、CD8 + T细胞和CD161 + NK细胞数量减少。此外,与野生型大鼠相比,所有基因敲除品系的相对脾脏重量均降低,白髓生发中心发育不全,胸腺皮质与髓质边界消失且出现萎缩。此外,我们通过向Il2rg/Rag2基因敲除大鼠静脉注射5.0×10个细胞/千克的NALM6细胞,建立了人急性淋巴细胞白血病异种移植大鼠模型。

结论

这些发现表明,Il2rg基因敲除、Rag2基因敲除和Il2rg/Rag2基因敲除大鼠表现出SCID表型,表明它们作为肿瘤异种移植研究的免疫缺陷动物模型具有潜在应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd5/11673691/a65b806f8bd1/42826_2024_231_Fig1_HTML.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