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B6-hCD40LG Mouse
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B6-hCD40LG Mouse
제품명
B6-hCD40LG Mouse
제품 ID
C001720
품종 계통
C57BL/6NCya-Cd40lgtm1(hCD40LG)/Cya
Backgroud
C57BL/6NCya
상태
이 마우스 계통을 논문에서 사용할 경우, “B6-hCD40LG Mouse (카탈로그 번호 C001720)은 Cyagen에서 구입하였습니다.”라고 명시해 주시기 바랍니다.
HUGO-GT Humanized Models
Immune Target Humanized Mouse Models
Systemic Lupus Erythematosus
구매 가능한 제품 종류
연령
Genotype
성별
수량
표준 제공 조건은 최소 3마리의 이형접합(heterozygous) 보균자를 보장합니다. 동형접합(homozygous) 보균자 및/또는 특정 성별에 대한 브리딩 서비스도 제공됩니다.
가격 문의
HUGO-GT Humanized Models
Immune Target Humanized Mouse Models
Systemic Lupus Erythematosus
기본 정보
관련 자료
기본 정보
유전자명
유전자 별칭
IGM, IMD3, TRAP, gp39, CD154, CD40L, HIGM1, T-BAM, TNFSF5, hCD40L
NCBI ID
염색체
Chr X
MGI ID
Datasheet
품종 계통 설명
The CD40LG gene is located on the X chromosome (Xq26.3) and encodes CD40 ligand (CD40L, also known as CD154), a type II transmembrane protein mainly expressed on activated T cells, platelets, and some B cells. Under inflammatory conditions, monocytes, natural killer cells, mast cells, and basophils can also be induced to express CD40L [1-3]. This protein binds to CD40 on the surface of antigen-presenting cells (such as B cells and dendritic cells), mediating key immune functions including T cell-dependent B cell activation, immunoglobulin class switching, and germinal center formation [3]. The CD40/CD40L interaction also regulates thrombosis, inflammatory responses, hematopoiesis, and the tumor immune microenvironment. Abnormal regulation of CD40LG is associated with X-linked hyper-IgM syndrome (XHIGM), a primary immunodeficiency disease characterized by recurrent infections due to defective antibody production [4]. In addition, abnormal expression of CD40L is involved in diseases such as systemic lupus erythematosus and atherosclerosis through its pro-inflammatory effects [5-6]. Due to the important role of the CD40/CD40L interaction in immune activation, CD40/CD40L has been an important target for immunotherapy. In recent years, significant progress has been made in CD40/CD40L-targeted therapy. Various drugs have been developed, including agonistic/antagonistic monoclonal antibodies, cellular vaccines, adenoviral vectors, and protein antagonists, and have shown therapeutic potential in malignant tumors, autoimmune diseases, and allograft rejection [7].
The B6-hCD40LG mice are a humanized model constructed by using gene editing technology to replace the endogenous extracellular domain of the mouse Cd40lg gene with the extracellular domain of the human CD40LG gene. This model can be used for research on the disease mechanisms and treatment methods of autoimmune diseases, cardiovascular diseases, cancers, etc., as well as for CD40LG-targeted drug development.
Reference
Grewal IS, Flavell RA. CD40 and CD154 in cell-mediated immunity. Annu Rev Immunol. 1998;16:111-35.
Henn V, Slupsky JR, Gräfe M, Anagnostopoulos I, Förster R, Müller-Berghaus G, Kroczek RA. CD40 ligand on activated platelets triggers an inflammatory reaction of endothelial cells. Nature. 1998 Feb 5;391(6667):591-4.
Elgueta R, Benson MJ, de Vries VC, Wasiuk A, Guo Y, Noelle RJ. Molecular mechanism and function of CD40/CD40L engagement in the immune system. Immunol Rev. 2009 May;229(1):152-72.
Meng X, Yang B, Suen WC. Prospects for modulating the CD40/CD40L pathway in the therapy of the hyper-IgM syndrome. Innate Immun. 2018 Jan;24(1):4-10.
Ramanujam M, Steffgen J, Visvanathan S, Mohan C, Fine JS, Putterman C. Phoenix from the flames: Rediscovering the role of the CD40-CD40L pathway in systemic lupus erythematosus and lupus nephritis. Autoimmun Rev. 2020 Nov;19(11):102668.
Lutgens E, Daemen MJ. CD40-CD40L interactions in atherosclerosis. Trends Cardiovasc Med. 2002 Jan;12(1):27-32.
Tang T, Cheng X, Truong B, Sun L, Yang X, Wang H. Molecular basis and therapeutic implications of CD40/CD40L immune checkpoint. Pharmacol Ther. 2021 Mar;219:107709.
변형 전략

Figure 1. Gene editing strategy of B6-hCD40LG mice. The mouse Cd40lg endogenous extracellular domain was replaced with the human CD40LG extracellular domain. The murine transmembrane-cytoplasmic region was be preserved.
응용 분야
Screening, development, and preclinical efficacy evaluation of CD40LG-targeted drugs;
Research on the pathological mechanisms and treatment methods of autoimmune diseases such as systemic lupus erythematosus (SLE) and lupus nephritis (LN);
Research on cardiovascular diseases, cancers, etc.
관련 자료
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