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Former Names CNCr.129P2-Tnfrsf5tm1Kik/J (Changed: 30-SEP-05 ) Cd40 (Changed: 15-DEC-04 ) Type Congenic; Mutant Strain; Targeted Mutation; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Additional information on Congenic nomenclature. Species laboratory mouse Background Strain BALB/cAnNcr Donor Strain 129P2 via E14-1 ES cell line Generation ?+F1p (03-JUL-05)
Generation DefinitionsDonating Investigator Hitoshi Kikutani, Osaka University Appearance
albino
Related Genotype: Tyrp1b/Tyrp1b Tyrc/TyrcDescription
Mice homozygous for the targeted mutation are viable and fertile. Homozygous mutant mice exhibit impaired immunoglobulin class switching and germinal center formation.
| Control | ||
|---|---|---|
| See control note: | The Jackson Laboratory does not have the BALB/cAnNcr substrain. BALB/cByJ mice(Stock No. 001026) are the most closely related substrain and may be used as a control although we have not tested histocompatibility between the two strains. | |
| 001026 BALB/cByJ | ||
| Considerations for Choosing Controls | ||
Strains carrying Cd40tm1Kik allele
002928 B6.129P2-Cd40tm1Kik/J View Strains carrying Cd40tm1Kik (1 strain)
Strains carrying other alleles of Cd40
002928 B6.129P2-Cd40tm1Kik/J View Strains carrying other alleles of Cd40 (1 strain)
View Mammalian Phenotype Terms
Mammalian Phenotype Terms provided by MGI
assigned by genotype
The following phenotype information may relate to a genetic background differing from this JAX® Mice strain.
Cd40tm1Kik/Cd40tm1Kik
B6.129P2-Cd40tm1Kik/J
- hematopoietic system phenotype
- *normal* hematopoietic system phenotype
- normal thrombogenesis in ferric-chloride-induced injury of mesenteric arterioles (MGI Ref ID J:75152)
- immune system phenotype
- abnormal dendritic cell physiology
- increased susceptibility to bacterial infection
Cd40tm1Kik/Cd40tm1Kik
involves: 129P2/OlaHsd * C57BL/6
- hematopoietic system phenotype
- absent spleen germinal center
- failed to form (MGI Ref ID J:25007)
- decreased neutrophil cell number
- in non-SPF facilities compared to wild-type controls (MGI Ref ID J:25007)
- immune system phenotype
- *normal* immune system phenotype
- normal numbers and ratios of T and B cells (MGI Ref ID J:25007)
- abnormal humoral immune response (MGI Ref ID J:25007)
- decreased immunoglobulin level
- decreased IgA level
- decreased IgE level
- decreased IgG1 level
- decreased IgG2a level
- decreased IgG2b level
- decreased IgG3 level
- absent spleen germinal center
- failed to form (MGI Ref ID J:25007)
- decreased neutrophil cell number
- in non-SPF facilities compared to wild-type controls (MGI Ref ID J:25007)
- decreased susceptibility to type II hypersensitivity reaction
- in model of accelerated anti-glomerular basement membrane antibody-mediated glomerulonephritis (MGI Ref ID J:61673)
- deposition of IgG and complement in glomeruli not observed (MGI Ref ID J:61673)
- glomeruli almost normal (MGI Ref ID J:61673)
- fibrin deposition in glomeruli not observed (MGI Ref ID J:61673)
- failure to induce proteinuria (MGI Ref ID J:61673)
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:
Cd40tm1Kik relatedSensorineural Research
Nociception
Cancer Research
Growth Factors/Receptors/Cytokines
Immunology and Inflammation Research
CD Antigens, Antigen Receptors, and Histocompatibility Markers
Growth Factors/Receptors/Cytokines
| Allele Symbol | Cd40tm1Kik | ||
|---|---|---|---|
| Allele Name | targeted mutation 1, Hitoshi Kikutani | ||
| Allele Type | Targeted (knock-out) | ||
| Common Name(s) | CD40 Ko; CD40-; CD40KO; Tnfrsf5-; Tnfrsf5tm1Kik; | ||
| Mutation Made By | Hitoshi Kikutani, Osaka University | ||
| Strain of Origin | 129P2/OlaHsd | ||
| ES Cell Line Name | E14.1 | ||
| ES Cell Line Strain | 129P2/OlaHsd | ||
| Gene Symbol and Name | Cd40, CD40 antigen | ||
| Chromosome | 2 | ||
| Gene Common Name(s) | AI326936; Bp50; CDW40; TNFRSF5; Tnfrsf5; expressed sequence AI326936; p50; tumor necrosis factor receptor superfamily, member 5; | ||
| Molecular Note | A neomycin cassette was inserted into exon 3. Disruption of the functionality of the protein was confirmed by a surface expression assay in spleen cells in which no binding of Tnfsf5 to ligand was observed. [MGI Ref ID J:25007] | ||
Genotyping Protocols
Cd40tm1Kik, Separated PCR
Helpful Links
Genotyping resources and troubleshooting
Kawabe T; Naka T; Yoshida K; Tanaka T; Fujiwara H; Suematsu S; Yoshida N; Kishimoto T; Kikutani H. 1994. The immune responses in CD40-deficient mice: impaired immunoglobulin class switching and germinal center formation. Immunity 1(3):167-78. [PubMed: 7534202] [MGI Ref ID J:25007]
Montfort MJ; Bouwer HG; Wagner CR; Hinrichs DJ. 2004. The development of functional CD8 T cell memory after Listeria monocytogenes infection is not dependent on CD40. J Immunol 173(6):4084-90. [PubMed: 15356158] [MGI Ref ID J:92749]
Ruedl C; Bachmann MF; Kopf M. 2000. The antigen dose determines T helper subset development by regulation of CD40 ligand. Eur J Immunol 30(7):2056-64. [PubMed: 10940895] [MGI Ref ID J:63646]
Cd40tm1Kik relatedAiba Y; Yamazaki T; Okada T; Gotoh K; Sanjo H; Ogata M; Kurosaki T. 2006. BANK negatively regulates Akt activation and subsequent B cell responses. Immunity 24(3):259-68. [PubMed: 16546095] [MGI Ref ID J:113321]
Akiba H; Takeda K; Kojima Y; Usui Y; Harada N; Yamazaki T; Ma J; Tezuka K; Yagita H; Okumura K. 2005. The role of ICOS in the CXCR5+ follicular B helper T cell maintenance in vivo. J Immunol 175(4):2340-8. [PubMed: 16081804] [MGI Ref ID J:107507]
Akiyama T; Shimo Y; Yanai H; Qin J; Ohshima D; Maruyama Y; Asaumi Y; Kitazawa J; Takayanagi H; Penninger JM; Matsumoto M; Nitta T; Takahama Y; Inoue J. 2008. The tumor necrosis factor family receptors RANK and CD40 cooperatively establish the thymic medullary microenvironment and self-tolerance. Immunity 29(3):423-37. [PubMed: 18799149] [MGI Ref ID J:139649]
Anderson BE; McNiff JM; Jain D; Blazar BR; Shlomchik WD; Shlomchik MJ. 2005. Distinct roles for donor- and host-derived antigen-presenting cells and costimulatory molecules in murine chronic graft-versus-host disease: requirements depend on target organ. Blood 105(5):2227-34. [PubMed: 15522961] [MGI Ref ID J:98140]
Andre P; Prasad KS; Denis CV; He M; Papalia JM; Hynes RO; Phillips DR; Wagner DD. 2002. CD40L stabilizes arterial thrombi by a beta3 integrin--dependent mechanism. Nat Med 8(3):247-52. [PubMed: 11875495] [MGI Ref ID J:75152]
Bachmann MF; Schwarz K; Wolint P; Meijerink E; Martin S; Manolova V; Oxenius A. 2004. Cutting edge: distinct roles for T help and CD40/CD40 ligand in regulating differentiation of proliferation-competent memory CD8+ T cells. J Immunol 173(4):2217-21. [PubMed: 15294930] [MGI Ref ID J:92734]
Bachmann MF; Wong BR; Josien R; Steinman RM; Oxenius A; Choi Y. 1999. TRANCE, a tumor necrosis factor family member critical for CD40 ligand-independent T helper cell activation. J Exp Med 189(7):1025-31. [PubMed: 10190893] [MGI Ref ID J:111460]
Bergthorsdottir S; Gallagher A; Jainandunsing S; Cockayne D; Sutton J; Leanderson T; Gray D. 2001. Signals that initiate somatic hypermutation of B cells in vitro. J Immunol 166(4):2228-34. [PubMed: 11160276] [MGI Ref ID J:127146]
Bessa J; Jegerlehner A; Hinton HJ; Pumpens P; Saudan P; Schneider P; Bachmann MF. 2009. Alveolar macrophages and lung dendritic cells sense RNA and drive mucosal IgA responses. J Immunol 183(6):3788-99. [PubMed: 19710454] [MGI Ref ID J:152307]
Bhadra R; Gigley JP; Khan IA. 2011. Cutting edge: CD40-CD40 ligand pathway plays a critical CD8-intrinsic and -extrinsic role during rescue of exhausted CD8 T cells. J Immunol 187(9):4421-5. [PubMed: 21949017] [MGI Ref ID J:179445]
Binstadt BA; Hebert JL; Ortiz-Lopez A; Bronson R; Benoist C; Mathis D. 2009. The same systemic autoimmune disease provokes arthritis and endocarditis via distinct mechanisms. Proc Natl Acad Sci U S A 106(39):16758-63. [PubMed: 19805369] [MGI Ref ID J:153217]
Bourgeois C; Rocha B; Tanchot C. 2002. A role for CD40 expression on CD8+ T cells in the generation of CD8+ T cell memory. Science 297(5589):2060-3. [PubMed: 12242444] [MGI Ref ID J:127835]
Buhlmann JE; Elkin SK; Sharpe AH. 2003. A Role for the B7-1/B7-2:CD28/CTLA-4 Pathway During Negative Selection. J Immunol 170(11):5421-8. [PubMed: 12759417] [MGI Ref ID J:83454]
Buhtoiarov IN; Lum HD; Berke G; Sondel PM; Rakhmilevich AL. 2006. Synergistic activation of macrophages via CD40 and TLR9 results in T cell independent antitumor effects. J Immunol 176(1):309-18. [PubMed: 16365423] [MGI Ref ID J:126263]
Burocchi A; Pittoni P; Gorzanelli A; Colombo MP; Piconese S. 2011. Intratumor OX40 stimulation inhibits IRF1 expression and IL-10 production by Treg cells while enhancing CD40L expression by effector memory T cells. Eur J Immunol 41(12):3615-26. [PubMed: 22229156] [MGI Ref ID J:179655]
Calzascia T; Pellegrini M; Lin A; Garza KM; Elford AR; Shahinian A; Ohashi PS; Mak TW. 2008. CD4 T cells, lymphopenia, and IL-7 in a multistep pathway to autoimmunity. Proc Natl Acad Sci U S A 105(8):2999-3004. [PubMed: 18287017] [MGI Ref ID J:132821]
Campos-Neto A; Ovendale P; Bement T; Koppi TA; Fanslow WC; Rossi MA; Alderson MR. 1998. CD40 ligand is not essential for the development of cell-mediated immunity and resistance to Mycobacterium tuberculosis. J Immunol 160(5):2037-41. [PubMed: 9498737] [MGI Ref ID J:123032]
Cao L; Palmer CD; Malon JT; De Leo JA. 2009. Critical role of microglial CD40 in the maintenance of mechanical hypersensitivity in a murine model of neuropathic pain. Eur J Immunol 39(12):3562-9. [PubMed: 19750482] [MGI Ref ID J:154932]
Carragher DM; Kaminski DA; Moquin A; Hartson L; Randall TD. 2008. A novel role for non-neutralizing antibodies against nucleoprotein in facilitating resistance to influenza virus. J Immunol 181(6):4168-76. [PubMed: 18768874] [MGI Ref ID J:139087]
Chen GH; Osterholzer JJ; Choe MY; McDonald RA; Olszewski MA; Huffnagle GB; Toews GB. 2010. Dual roles of CD40 on microbial containment and the development of immunopathology in response to persistent fungal infection in the lung. Am J Pathol 177(5):2459-71. [PubMed: 20864680] [MGI Ref ID J:166256]
Chen L; Arora M; Yarlagadda M; Oriss TB; Krishnamoorthy N; Ray A; Ray P. 2006. Distinct responses of lung and spleen dendritic cells to the TLR9 agonist CpG oligodeoxynucleotide. J Immunol 177(4):2373-83. [PubMed: 16887999] [MGI Ref ID J:138357]
Chen L; Cheng W; Shivshankar P; Lei L; Zhang X; Wu Y; Yeh IT; Zhong G. 2009. Distinct roles of CD28- and CD40 ligand-mediated costimulation in the development of protective immunity and pathology during Chlamydia muridarum urogenital infection in mice. Infect Immun 77(7):3080-9. [PubMed: 19398542] [MGI Ref ID J:150306]
Choi YS; Kageyama R; Eto D; Escobar TC; Johnston RJ; Monticelli L; Lao C; Crotty S. 2011. ICOS Receptor Instructs T Follicular Helper Cell versus Effector Cell Differentiation via Induction of the Transcriptional Repressor Bcl6. Immunity 34(6):932-46. [PubMed: 21636296] [MGI Ref ID J:174012]
Collins JT; Shi J; Burrell BE; Bishop DK; Dunnick WA. 2006. Induced expression of murine gamma2a by CD40 ligation independently of IFN-gamma. J Immunol 177(8):5414-9. [PubMed: 17015727] [MGI Ref ID J:139436]
Crawford A; Macleod M; Schumacher T; Corlett L; Gray D. 2006. Primary T cell expansion and differentiation in vivo requires antigen presentation by B cells. J Immunol 176(6):3498-506. [PubMed: 16517718] [MGI Ref ID J:129511]
Dautigny N; Le Campion A; Lucas B. 1999. Timing and casting for actors of thymic negative selection. J Immunol 162(3):1294-302. [PubMed: 9973382] [MGI Ref ID J:124433]
De Santo C; Salio M; Masri SH; Lee LY; Dong T; Speak AO; Porubsky S; Booth S; Veerapen N; Besra GS; Grone HJ; Platt FM; Zambon M; Cerundolo V. 2008. Invariant NKT cells reduce the immunosuppressive activity of influenza A virus-induced myeloid-derived suppressor cells in mice and humans. J Clin Invest 118(12):4036-48. [PubMed: 19033672] [MGI Ref ID J:144728]
Deenick EK; Chan A; Ma CS; Gatto D; Schwartzberg PL; Brink R; Tangye SG. 2010. Follicular helper T cell differentiation requires continuous antigen presentation that is independent of unique B cell signaling. Immunity 33(2):241-53. [PubMed: 20691615] [MGI Ref ID J:163920]
DiPaolo RJ; Unanue ER. 2002. Cutting edge: the relative distribution of T cells responding to chemically dominant or minor epitopes of lysozyme is not affected by CD40-CD40 ligand and B7-CD28-CTLA-4 costimulatory pathways. J Immunol 169(6):2832-6. [PubMed: 12218093] [MGI Ref ID J:120434]
Diaz-de-Durana Y; Mantchev GT; Bram RJ; Franco A. 2006. TACI-BLyS signaling via B-cell-dendritic cell cooperation is required for naive CD8+ T-cell priming in vivo. Blood 107(2):594-601. [PubMed: 16195331] [MGI Ref ID J:126637]
Enzler T; Bonizzi G; Silverman GJ; Otero DC; Widhopf GF; Anzelon-Mills A; Rickert RC; Karin M. 2006. Alternative and classical NF-kappa B signaling retain autoreactive B cells in the splenic marginal zone and result in lupus-like disease. Immunity 25(3):403-15. [PubMed: 16973390] [MGI Ref ID J:113556]
Fang M; Sigal LJ. 2005. Antibodies and CD8+ T cells are complementary and essential for natural resistance to a highly lethal cytopathic virus. J Immunol 175(10):6829-36. [PubMed: 16272340] [MGI Ref ID J:119697]
Fillatreau S; Gray D. 2003. T cell accumulation in B cell follicles is regulated by dendritic cells and is independent of B cell activation. J Exp Med 197(2):195-206. [PubMed: 12538659] [MGI Ref ID J:124822]
Florido M; Goncalves AS; Gomes MS; Appelberg R. 2004. CD40 is required for the optimal induction of protective immunity to Mycobacterium avium. Immunology 111(3):323-7. [PubMed: 15009433] [MGI Ref ID J:88471]
Fuse S; Tsai CY; Molloy MJ; Allie SR; Zhang W; Yagita H; Usherwood EJ. 2009. Recall responses by helpless memory CD8+ T cells are restricted by the up-regulation of PD-1. J Immunol 182(7):4244-54. [PubMed: 19299723] [MGI Ref ID J:147123]
Gaspal FM; McConnell FM; Kim MY; Gray D; Kosco-Vilbois MH; Raykundalia CR; Botto M; Lane PJ. 2006. The generation of thymus-independent germinal centers depends on CD40 but not on CD154, the T cell-derived CD40-ligand. Eur J Immunol 36(7):1665-73. [PubMed: 16783845] [MGI Ref ID J:115798]
Giannoni F; Shea A; Inglis C; Lee LN; Sarawar SR. 2008. CD40 engagement on dendritic cells, but not on B or T cells, is required for long-term control of murine gammaherpesvirus 68. J Virol 82(22):11016-22. [PubMed: 18768977] [MGI Ref ID J:142958]
Glauert HP; Eyigor A; Tharappel JC; Cooper S; Lee EY; Spear BT. 2006. Inhibition of hepatocarcinogenesis by the deletion of the p50 subunit of NF-kappaB in mice administered the peroxisome proliferator Wy-14,643. Toxicol Sci 90(2):331-6. [PubMed: 16434500] [MGI Ref ID J:113288]
Guarda G; Dostert C; Staehli F; Cabalzar K; Castillo R; Tardivel A; Schneider P; Tschopp J. 2009. T cells dampen innate immune responses through inhibition of NLRP1 and NLRP3 inflammasomes. Nature 460(7252):269-73. [PubMed: 19494813] [MGI Ref ID J:150357]
Guiducci C; Valzasina B; Dislich H; Colombo MP. 2005. CD40/CD40L interaction regulates CD4(+)CD25(+) T reg homeostasis through dendritic cell-produced IL-2. Eur J Immunol 35(2):557-67. [PubMed: 15682445] [MGI Ref ID J:95614]
Gupta S; Boppana R; Mishra GC; Saha B; Mitra D. 2008. Interleukin-12 is necessary for the priming of CD4+ T cells required during the elicitation of HIV-1 gp120-specific cytotoxic T-lymphocyte function. Immunology 124(4):553-61. [PubMed: 18298551] [MGI Ref ID J:142777]
Hao S; Yuan J; Xiang J. 2007. Nonspecific CD4+ T cells with uptake of antigen-specific dendritic cell-released exosomes stimulate antigen-specific CD8+ CTL responses and long-term T cell memory. J Leukoc Biol 82(4):829-38. [PubMed: 17626150] [MGI Ref ID J:125204]
Hashimoto N; Kawabe T; Imaizumi K; Hara T; Okamoto M; Kojima K; Shimokata K; Hasegawa Y. 2004. CD40 plays a crucial role in lipopolysaccharide-induced acute lung injury. Am J Respir Cell Mol Biol 30(6):808-15. [PubMed: 14693668] [MGI Ref ID J:99677]
Hayakawa Y; Takeda K; Yagita H; Van Kaer L; Saiki I; Okumura K. 2001. Differential regulation of Th1 and Th2 functions of NKT cells by CD28 and CD40 costimulatory pathways. J Immunol 166(10):6012-8. [PubMed: 11342617] [MGI Ref ID J:110892]
Heer AK; Shamshiev A; Donda A; Uematsu S; Akira S; Kopf M; Marsland BJ. 2007. TLR signaling fine-tunes anti-influenza B cell responses without regulating effector T cell responses. J Immunol 178(4):2182-91. [PubMed: 17277123] [MGI Ref ID J:143991]
Hernandez MG; Shen L; Rock KL. 2008. CD40 on APCs Is Needed for Optimal Programming, Maintenance, and Recall of CD8+ T Cell Memory Even in the Absence of CD4+ T Cell Help. J Immunol 180(7):4382-90. [PubMed: 18354158] [MGI Ref ID J:132973]
Hernandez MG; Shen L; Rock KL. 2007. CD40-CD40 ligand interaction between dendritic cells and CD8+ T cells is needed to stimulate maximal T cell responses in the absence of CD4+ T cell help. J Immunol 178(5):2844-52. [PubMed: 17312128] [MGI Ref ID J:144111]
Higuchi T; Aiba Y; Nomura T; Matsuda J; Mochida K; Suzuki M; Kikutani H; Honjo T; Nishioka K; Tsubata T. 2002. Cutting Edge: Ectopic expression of CD40 ligand on B cells induces lupus-like autoimmune disease. J Immunol 168(1):9-12. [PubMed: 11751940] [MGI Ref ID J:128824]
Hikosaka Y; Nitta T; Ohigashi I; Yano K; Ishimaru N; Hayashi Y; Matsumoto M; Matsuo K; Penninger JM; Takayanagi H; Yokota Y; Yamada H; Yoshikai Y; Inoue J; Akiyama T; Takahama Y. 2008. The cytokine RANKL produced by positively selected thymocytes fosters medullary thymic epithelial cells that express autoimmune regulator. Immunity 29(3):438-50. [PubMed: 18799150] [MGI Ref ID J:139648]
Hochweller K; Anderton SM. 2004. Systemic administration of antigen-loaded CD40-deficient dendritic cells mimics soluble antigen administration. Eur J Immunol 34(4):990-8. [PubMed: 15048709] [MGI Ref ID J:88882]
Hochweller K; Sweenie CH; Anderton SM. 2006. Circumventing tolerance at the T cell or the antigen-presenting cell surface: antibodies that ligate CD40 and OX40 have different effects. Eur J Immunol 36(2):389-96. [PubMed: 16402409] [MGI Ref ID J:113856]
Hou H; Obregon D; Lou D; Ehrhart J; Fernandez F; Silver A; Tan J. 2008. Modulation of neuronal differentiation by CD40 isoforms. Biochem Biophys Res Commun 369(2):641-7. [PubMed: 18312851] [MGI Ref ID J:134173]
Idoyaga J; Lubkin A; Fiorese C; Lahoud MH; Caminschi I; Huang Y; Rodriguez A; Clausen BE; Park CG; Trumpfheller C; Steinman RM. 2011. Comparable T helper 1 (Th1) and CD8 T-cell immunity by targeting HIV gag p24 to CD8 dendritic cells within antibodies to Langerin, DEC205, and Clec9A. Proc Natl Acad Sci U S A 108(6):2384-9. [PubMed: 21262813] [MGI Ref ID J:169105]
Inoue S; Leitner WW; Golding B; Scott D. 2006. Inhibitory effects of B cells on antitumor immunity. Cancer Res 66(15):7741-7. [PubMed: 16885377] [MGI Ref ID J:112103]
Irla M; Hugues S; Gill J; Nitta T; Hikosaka Y; Williams IR; Hubert FX; Scott HS; Takahama Y; Hollander GA; Reith W. 2008. Autoantigen-specific interactions with CD4+ thymocytes control mature medullary thymic epithelial cell cellularity. Immunity 29(3):451-63. [PubMed: 18799151] [MGI Ref ID J:139647]
Ishikawa M; Vowinkel T; Stokes KY; Arumugam TV; Yilmaz G; Nanda A; Granger DN. 2005. CD40/CD40 ligand signaling in mouse cerebral microvasculature after focal ischemia/reperfusion. Circulation 111(13):1690-6. [PubMed: 15795333] [MGI Ref ID J:108988]
Jenkins SJ; Perona-Wright G; MacDonald AS. 2008. Full development of Th2 immunity requires both innate and adaptive sources of CD154. J Immunol 180(12):8083-92. [PubMed: 18523272] [MGI Ref ID J:137237]
Jeurissen A; Billiau AD; Moens L; Shengqiao L; Landuyt W; Wuyts G; Boon L; Waer M; Ceuppens JL; Bossuyt X. 2006. CD4+ T lymphocytes expressing CD40 ligand help the IgM antibody response to soluble pneumococcal polysaccharides via an intermediate cell type. J Immunol 176(1):529-36. [PubMed: 16365447] [MGI Ref ID J:126613]
Kastenmuller W; Gasteiger G; Subramanian N; Sparwasser T; Busch DH; Belkaid Y; Drexler I; Germain RN. 2011. Regulatory T cells selectively control CD8+ T cell effector pool size via IL-2 restriction. J Immunol 187(6):3186-97. [PubMed: 21849683] [MGI Ref ID J:179230]
Kawamura T; Kanai T; Dohi T; Uraushihara K; Totsuka T; Iiyama R; Taneda C; Yamazaki M; Nakamura T; Higuchi T; Aiba Y; Tsubata T; Watanabe M. 2004. Ectopic CD40 ligand expression on B cells triggers intestinal inflammation. J Immunol 172(10):6388-97. [PubMed: 15128830] [MGI Ref ID J:89855]
Khiong K; Murakami M; Kitabayashi C; Ueda N; Sawa S; Sakamoto A; Kotzin BL; Rozzo SJ; Ishihara K; Verella-Garcia M; Kappler J; Marrack P; Hirano T. 2007. Homeostatically proliferating CD4 T cells are involved in the pathogenesis of an Omenn syndrome murine model. J Clin Invest 117(5):1270-81. [PubMed: 17476359] [MGI Ref ID J:122142]
Kishi Y; Aiba Y; Higuchi T; Furukawa K; Tokuhisa T; Takemori T; Tsubata T. 2010. Augmented antibody response with premature germinal center regression in CD40L transgenic mice. J Immunol 185(1):211-9. [PubMed: 20505144] [MGI Ref ID J:161443]
Kobayashi T; Kim TS; Jacob A; Walsh MC; Kadono Y; Fuentes-Panana E; Yoshioka T; Yoshimura A; Yamamoto M; Kaisho T; Akira S; Monroe JG; Choi Y. 2009. TRAF6 is required for generation of the B-1a B cell compartment as well as T cell-dependent and -independent humoral immune responses. PLoS ONE 4(3):e4736. [PubMed: 19270748] [MGI Ref ID J:147371]
Koschella M; Voehringer D; Pircher H. 2004. CD40 ligation in vivo induces bystander proliferation of memory phenotype CD8 T cells. J Immunol 172(8):4804-11. [PubMed: 15067057] [MGI Ref ID J:89113]
Kraus ZJ; Nakano H; Bishop GA. 2009. TRAF5 is a critical mediator of in vitro signals and in vivo functions of LMP1, the viral oncogenic mimic of CD40. Proc Natl Acad Sci U S A 106(40):17140-5. [PubMed: 19805155] [MGI Ref ID J:153675]
Kurche JS; Burchill MA; Sanchez PJ; Haluszczak C; Kedl RM. 2010. Comparison of OX40 Ligand and CD70 in the Promotion of CD4+ T Cell Responses. J Immunol 185(4):2106-15. [PubMed: 20639485] [MGI Ref ID J:162543]
Kuwajima S; Sato T; Ishida K; Tada H; Tezuka H; Ohteki T. 2006. Interleukin 15-dependent crosstalk between conventional and plasmacytoid dendritic cells is essential for CpG-induced immune activation. Nat Immunol 7(7):740-6. [PubMed: 16715101] [MGI Ref ID J:112665]
Laporte V; Ait-Ghezala G; Volmar CH; Ganey C; Ganey N; Wood M; Mullan M. 2008. CD40 ligation mediates plaque-associated tau phosphorylation in beta-amyloid overproducing mice. Brain Res 1231:132-42. [PubMed: 18606155] [MGI Ref ID J:139872]
Lazarevic V; Myers AJ; Scanga CA; Flynn JL. 2003. CD40, but not CD40L, is required for the optimal priming of T cells and control of aerosol M. tuberculosis infection. Immunity 19(6):823-35. [PubMed: 14670300] [MGI Ref ID J:86998]
Lee BO; Rangel-Moreno J; Moyron-Quiroz JE; Hartson L; Makris M; Sprague F; Lund FE; Randall TD. 2005. CD4 T cell-independent antibody response promotes resolution of primary influenza infection and helps to prevent reinfection. J Immunol 175(9):5827-38. [PubMed: 16237075] [MGI Ref ID J:119355]
Li H; Matte-Martone C; Tan HS; Venkatesan S; McNiff J; Demetris AJ; Jain D; Lakkis F; Rothstein D; Shlomchik WD. 2011. Graft-versus-host disease is independent of innate signaling pathways triggered by pathogens in host hematopoietic cells. J Immunol 186(1):230-41. [PubMed: 21098219] [MGI Ref ID J:168013]
Li W; Buzoni-Gatel D; Debbabi H; Hu MS; Mennechet FJ; Durell BG; Noelle RJ; Kasper LH. 2002. CD40/CD154 ligation is required for the development of acute ileitis following oral infection with an intracellular pathogen in mice. Gastroenterology 122(3):762-73. [PubMed: 11875009] [MGI Ref ID J:75019]
Li Y; Toraldo G; Li A; Yang X; Zhang H; Qian WP; Weitzmann MN. 2007. B cells and T cells are critical for the preservation of bone homeostasis and attainment of peak bone mass in vivo. Blood 109(9):3839-48. [PubMed: 17202317] [MGI Ref ID J:145330]
Lievens D; Zernecke A; Seijkens T; Soehnlein O; Beckers L; Munnix IC; Wijnands E; Goossens P; van Kruchten R; Thevissen L; Boon L; Flavell RA; Noelle RJ; Gerdes N; Biessen EA; Daemen MJ; Heemskerk JW; Weber C; Lutgens E. 2010. Platelet CD40L mediates thrombotic and inflammatory processes in atherosclerosis. Blood 116(20):4317-27. [PubMed: 20705757] [MGI Ref ID J:166644]
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Shi S; Blumenthal A; Hickey CM; Gandotra S; Levy D; Ehrt S. 2005. Expression of many immunologically important genes in Mycobacterium tuberculosis-infected macrophages is independent of both TLR2 and TLR4 but dependent on IFN-alphabeta receptor and STAT1. J Immunol 175(5):3318-28. [PubMed: 16116224] [MGI Ref ID J:113220]
Shibasaki M; Hashimoto K; Okamoto M; Hayashi Y; Imaizumi K; Hashimoto N; Ozaki N; Yokoi T; Takagi K; Hasegawa Y; Shimokata K; Kawabe T. 2009. Up-regulation of surfactant protein production in a mouse model of secondary pulmonary alveolar proteinosis. Am J Respir Cell Mol Biol 40(5):536-42. [PubMed: 18931325] [MGI Ref ID J:160868]
Shimizu K; Asakura M; Fujii S. 2011. Prolonged antitumor NK cell reactivity elicited by CXCL10-expressing dendritic cells licensed by CD40L+ CD4+ memory T cells. J Immunol 186(10):5927-37. [PubMed: 21460206] [MGI Ref ID J:173107]
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Srivastava N; Sudan R; Saha B. 2011. CD40-modulated dual-specificity phosphatases MAPK phosphatase (MKP)-1 and MKP-3 reciprocally regulate Leishmania major infection. J Immunol 186(10):5863-72. [PubMed: 21471446] [MGI Ref ID J:173097]
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Animal Health Reports
Production of mice from cryopreserved embryos or sperm occurs in a maximum barrier room, RG10/RG30.Colony Maintenance
Diet Information LabDiet® 5K52/5K67
| Pricing for USA, Canada and Mexico shipping destinations |
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Cryopreserved Mice - Ready for Recovery
Animals Provided
Price (US dollars $) Cryorecovery* $1980.00 At least two mice that carry the mutation (if it is a mutant strain) will be provided. Their genotypes may not reflect those discussed in the strain description. Please inquire for possible genotypes and see additional details below.
Standard Supply
Cryopreserved. Ready for recovery. Please refer to pricing and supply notes for further information.
Supply Notes
- Cryorecovery - Standard.
We will fulfill your order by providing at least two pair of mice, at least one animal of each pair carrying the mutation of interest. The total number of animals provided, their gender and genotype will vary. Please inquire if larger numbers of animals with specific genotype and genders are needed. Animals typically ship between 13 and 16 weeks from the date of your order. If a second cryorecovery is needed in order to provide the minimum number of animals, animals will ship within 25 weeks. IMPORTANT NOTE: The genotypes of animals provided may not reflect the mating scheme utilized by The Jackson Laboratory prior to cryopreservation, or that discussed in the strain description. Please inquire about possible genotypes which will be recovered for this specific strain. The Jackson Laboratory cannot guarantee the reproductive success of mice shipped to your facility. If the mice are lost after the first three days (post-arrival) or do not produce progeny at your facility, a new order and fee will be necessary.Cryorecovery to establish a Dedicated Supply for greater quantities of mice.
Mice recovered can be used to establish a dedicated colony to contractually supply you mice according to your requirements. Price by quotation. For more information on Dedicated Supply, please contact JAX® Services, Tel: 1-800-422-6423 (from U.S.A., Canada or Puerto Rico only) or 1-207-288-5845 (from any location).
| Pricing for International shipping destinations |
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Cryopreserved Mice - Ready for Recovery
Animals Provided
Price (US dollars $) Cryorecovery* $2574.00 At least two mice that carry the mutation (if it is a mutant strain) will be provided. Their genotypes may not reflect those discussed in the strain description. Please inquire for possible genotypes and see additional details below.
Standard Supply
Cryopreserved. Ready for recovery. Please refer to pricing and supply notes for further information.
Supply Notes
- Cryorecovery - Standard.
We will fulfill your order by providing at least two pair of mice, at least one animal of each pair carrying the mutation of interest. The total number of animals provided, their gender and genotype will vary. Please inquire if larger numbers of animals with specific genotype and genders are needed. Animals typically ship between 13 and 16 weeks from the date of your order. If a second cryorecovery is needed in order to provide the minimum number of animals, animals will ship within 25 weeks. IMPORTANT NOTE: The genotypes of animals provided may not reflect the mating scheme utilized by The Jackson Laboratory prior to cryopreservation, or that discussed in the strain description. Please inquire about possible genotypes which will be recovered for this specific strain. The Jackson Laboratory cannot guarantee the reproductive success of mice shipped to your facility. If the mice are lost after the first three days (post-arrival) or do not produce progeny at your facility, a new order and fee will be necessary.Cryorecovery to establish a Dedicated Supply for greater quantities of mice.
Mice recovered can be used to establish a dedicated colony to contractually supply you mice according to your requirements. Price by quotation. For more information on Dedicated Supply, please contact JAX® Services, Tel: 1-800-422-6423 (from U.S.A., Canada or Puerto Rico only) or 1-207-288-5845 (from any location).
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Cryopreserved. Ready for recovery. Please refer to pricing and supply notes for further information.
| Control | ||
|---|---|---|
| See control note: | The Jackson Laboratory does not have the BALB/cAnNcr substrain. BALB/cByJ mice(Stock No. 001026) are the most closely related substrain and may be used as a control although we have not tested histocompatibility between the two strains. | |
| 001026 BALB/cByJ | ||
| Considerations for Choosing Controls | ||
| Control Pricing Information for Genetically Engineered Mutant Strains. | ||
| phone: | 207-288-6470 |
| fax: | 207-288-6655 |
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