C57BL/6NCya-Lgmnem1/Cya
Common Name:
Lgmn-KO
Product ID:
S-KO-03803
Background:
C57BL/6NCya
Product Type
Age
Genotype
Sex
Quantity
Price:
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Basic Information
Strain Name
Lgmn-KO
Strain ID
KOCMP-19141-Lgmn-B6N-VA
Gene Name
Product ID
S-KO-03803
Gene Alias
AEP; Prsc1
Background
C57BL/6NCya
NCBI ID
Modification
Conventional knockout
Chromosome
12
Phenotype
Document
Application
--
Note: When using this mouse strain in a publication, please cite “C57BL/6NCya-Lgmnem1/Cya mice (Catalog S-KO-03803) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000021607
NCBI RefSeq
NM_011175
Target Region
Exon 4~11
Size of Effective Region
~7.7 kb
Detailed Document
Overview of Gene Research
Lgmn, also known as legumain, is an in vivo-active cysteine protease. It catalyzes the degradation of numerous proteins and is involved in multiple biological processes. Its functions include influencing the tumor microenvironment, cardiac repair, and extracellular matrix degradation, and it is associated with pathways such as those related to hypoxia-inducible factor 1-alpha (HIF1α) signaling, GSK-3β-STAT3 signaling, and chaperone-mediated autophagy. Genetic models, like knockout mice, have been crucial in studying its functions [1,2,3].
In multiple knockout and conditional knockout mouse models, Lgmn deficiency has shown various impacts. In myocardial infarction, Lgmn-deficient mice had exacerbated cardiac function, apoptotic cardiomyocyte accumulation, and reduced in vivo efferocytosis, highlighting its role in cardiac repair [2]. In thoracic aortic dissection (TAD), Lgmn-deficient or inhibited mice had ameliorated BAPN-induced TAD progression, indicating its role in VSMC phenotype transformation and TAD development [3]. In acute kidney injury (AKI), Lgmn-deficient mice had attenuated acute tubular injury, inflammation, and ferroptosis, suggesting its role in promoting tubular ferroptosis [4].
In conclusion, Lgmn is essential in processes such as cardiac repair, TAD development, and AKI-related tubular ferroptosis. Gene knockout and conditional knockout mouse models have significantly contributed to understanding Lgmn's role in these disease areas, providing potential therapeutic targets for myocardial infarction, TAD, and AKI [2,3,4].
References:
1. Khan, Safir Ullah, Khan, Ibrar Muhammad, Khan, Munir Ullah, Khan, Nazir Muhammad, Liu, Yong. 2023. Role of LGMN in tumor development and its progression and connection with the tumor microenvironment. In Frontiers in molecular biosciences, 10, 1121964. doi:10.3389/fmolb.2023.1121964. https://pubmed.ncbi.nlm.nih.gov/36825203/
2. Jia, Daile, Chen, Siqin, Bai, Peiyuan, Sun, Aijun, Ge, Junbo. 2022. Cardiac Resident Macrophage-Derived Legumain Improves Cardiac Repair by Promoting Clearance and Degradation of Apoptotic Cardiomyocytes After Myocardial Infarction. In Circulation, 145, 1542-1556. doi:10.1161/CIRCULATIONAHA.121.057549. https://pubmed.ncbi.nlm.nih.gov/35430895/
3. Pan, Lihong, Bai, Peiyuan, Weng, Xinyu, Sun, Aijun, Ge, Junbo. 2022. Legumain Is an Endogenous Modulator of Integrin αvβ3 Triggering Vascular Degeneration, Dissection, and Rupture. In Circulation, 145, 659-674. doi:10.1161/CIRCULATIONAHA.121.056640. https://pubmed.ncbi.nlm.nih.gov/35100526/
4. Chen, Chuan'ai, Wang, Dekun, Yu, Yangyang, Yue, Shijing, Tan, Xiaoyue. 2021. Legumain promotes tubular ferroptosis by facilitating chaperone-mediated autophagy of GPX4 in AKI. In Cell death & disease, 12, 65. doi:10.1038/s41419-020-03362-4. https://pubmed.ncbi.nlm.nih.gov/33431801/
Quality Control Standard
Sperm Test
Pre-cryopreservation: Measurement of sperm concentration, determination of sperm viability.
Post-cryopreservation: A vial of cryopreserved sperms is selected for in-vitro fertilization from each batch.
Environmental Standards:SPF
Available Region:Global
Source:Cyagen