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Type Mutant Stock; Targeted Mutation; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Species laboratory mouse Donating Investigator Tak Mak, University Health Network/Un of Toronto Appearance
black
Related Genotype: a/aDescription
Mice homozygous for both the Cd4tm1Mak and Cd8atm1Mak targeted mutations have a significant block in both CD4+ and CD8+ T-cell development. Homozygous mutant mice also show a Class II restricted deficit in helper T-cell activity and other T-cell responses.
| Control | ||
|---|---|---|
| 101045 B6129SF2/J | (approximate) | |
| Considerations for Choosing Controls | ||
Strains carrying Cd4tm1Mak allele
002663 B6.129S2-Cd4tm1Mak/J 006483 CBy.129S2(B6)-Cd4tm1Mak/J View Strains carrying Cd4tm1Mak (2 strains)
Strains carrying Cd8atm1Mak allele
002665 B6.129S2-Cd8atm1Mak/J 007071 CByJ.129S2(B6)-Cd8atm1Mak/J 005513 NOD.129S2(B6)-Cd8atm1Mak/DvsJ View Strains carrying Cd8atm1Mak (3 strains)
Strains carrying other alleles of Cd4
002447 B10.129S2(B6)-Cd4tm1Litt/J 010514 B10.Cg-H2g Tg(Cd4-Klra1)6295Dl/J 002663 B6.129S2-Cd4tm1Mak/J 002269 B6.129S6-Cd4tm1Knw/J 002268 B6;129S6-Cd4tm1Knw/J 012895 C57BL/6-Tg(Cd4-Il17rb)5Cdon/J 014639 C57BL/6-Tg(Cd4-TcraDN32D3)1Aben/J 014644 C57BL/6-Tg(Cd4-Zbtb16)1797Aben/J 006483 CBy.129S2(B6)-Cd4tm1Mak/J 003090 NOD.129S6(B6)-Cd4tm1Knw/DvsJ 005328 NOD/ShiLt-Tg(Cd4-DsRed)4Lt/J View Strains carrying other alleles of Cd4 (11 strains)
Strains carrying other alleles of Cd8a
017562 B6(Cg)-Cd8atm1.1(cre)Koni/J 002665 B6.129S2-Cd8atm1Mak/J 000407 B6.PL-Cd8aa Cd8b1a/(75NS)CyJ 001065 B6.PL-Cd8aa Cd8b1a/(85NS)CyJ 008766 C57BL/6-Tg(Cd8a-cre)1Itan/J 007071 CByJ.129S2(B6)-Cd8atm1Mak/J 005513 NOD.129S2(B6)-Cd8atm1Mak/DvsJ View Strains carrying other alleles of Cd8a (7 strains)
View Mammalian Phenotype Terms
Mammalian Phenotype Terms provided by MGI
assigned by genotype
Cd4tm1Mak/Cd4tm1Mak Cd8atm1Mak/Cd8atm1Mak
involves: 129S2/SvPas * C57BL/6 * DBA/2
- immune system phenotype
- abnormal T cell differentiation
- there is a 5-fold drop in the number of mature alphabeta TCR+ HAS- T cells in the thymus (MGI Ref ID J:12572)
- alphabeta TCR expression on these mature double negative cells is lower than in mature T cells of wild-type mice (MGI Ref ID J:12572)
- despite lack of CD4 and CD8 expression, alphabeta T cells are still present in the periphery (MGI Ref ID J:12572)
- abnormal T cell number
- the alphabeta T cell number in lymph nodes varies from 5% to 50% of normal (MGI Ref ID J:12572)
- abnormal thymus medulla morphology
- the medulla is reduced in size (MGI Ref ID J:12572)
- defective cytotoxic T cell cytolysis
- LCMV-specific class I MHC-restricted cytotoxic T cell responses are not activated in these mice (MGI Ref ID J:12572)
- alloantigen specific lysis of target cells by T cells in mixed lymphocyte culture is reduced (MGI Ref ID J:12572)
- the lysis of cells is specific for class I MHC antigens (MGI Ref ID J:12572)
- increased length of allograft survival
- tail skin graphs from donor mice of the same MHC haplotypes are not rejected within a three month period compared to controls that have no graph survival after 18 days (MGI Ref ID J:12572)
- when donor mice have a different MHC haplotype, skin graft rejection is similar to controls (MGI Ref ID J:12572)
- hematopoietic system phenotype
- abnormal T cell differentiation
- there is a 5-fold drop in the number of mature alphabeta TCR+ HAS- T cells in the thymus (MGI Ref ID J:12572)
- alphabeta TCR expression on these mature double negative cells is lower than in mature T cells of wild-type mice (MGI Ref ID J:12572)
- despite lack of CD4 and CD8 expression, alphabeta T cells are still present in the periphery (MGI Ref ID J:12572)
- abnormal T cell number
- the alphabeta T cell number in lymph nodes varies from 5% to 50% of normal (MGI Ref ID J:12572)
- abnormal thymus medulla morphology
- the medulla is reduced in size (MGI Ref ID J:12572)
- cellular phenotype
- abnormal T cell differentiation
- there is a 5-fold drop in the number of mature alphabeta TCR+ HAS- T cells in the thymus (MGI Ref ID J:12572)
- alphabeta TCR expression on these mature double negative cells is lower than in mature T cells of wild-type mice (MGI Ref ID J:12572)
- despite lack of CD4 and CD8 expression, alphabeta T cells are still present in the periphery (MGI Ref ID J:12572)
The following phenotype information may relate to a genetic background differing from this JAX® Mice strain.
Cd4tm1Mak/Cd4tm1Mak Cd8atm1Mak/Cd8atm1Mak
involves: 129S2/SvPas
- immune system phenotype
- increased susceptibility to viral infection
- virus is still detectable in bone marrow, heart, and other organs 1 month after polyomavirus infection compared to controls that clear the infection by one month (MGI Ref ID J:110749)
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:Cd4tm1Mak related
Cd8atm1Mak relatedImmunology and Inflammation Research
CD Antigens, Antigen Receptors, and Histocompatibility Markers
| Allele Symbol | Cd4tm1Mak | ||
|---|---|---|---|
| Allele Name | targeted mutation 1, Tak Mak | ||
| Allele Type | Targeted (knock-out) | ||
| Common Name(s) | CD4 KO; CD4-; CD40; | ||
| Mutation Made By | Tak Mak, University Health Network/Un of Toronto | ||
| Strain of Origin | 129S2/SvPas | ||
| ES Cell Line Name | D3 | ||
| ES Cell Line Strain | 129S2/SvPas | ||
| Gene Symbol and Name | Cd4, CD4 antigen | ||
| Chromosome | 6 | ||
| Gene Common Name(s) | CD4mut; L3T4; Ly-4; W3/25; lymphocyte antigen 4; p55; | ||
| Molecular Note | A neomycin resistance cassette was inserted into exon 5. Flow cytometry analysis demonstrated that the protein was absent from the cell surface of thymocytes and lymph node cells in homozygous mice. [MGI Ref ID J:68957] | ||
| Allele Symbol | Cd8atm1Mak | ||
| Allele Name | targeted mutation 1, Tak Mak | ||
| Allele Type | Targeted (knock-out) | ||
| Common Name(s) | CD8 KO; CD8-; CD8-KO; CD8KO; CD8alpha-; CD8alpha-; Cd8atm1Mak; Lyt-2-; | ||
| Mutation Made By | Tak Mak, University Health Network/Un of Toronto | ||
| Strain of Origin | 129S2/SvPas | ||
| ES Cell Line Name | D3 | ||
| ES Cell Line Strain | 129S2/SvPas | ||
| Gene Symbol and Name | Cd8a, CD8 antigen, alpha chain | ||
| Chromosome | 6 | ||
| Gene Common Name(s) | BB154331; CD8; Leu2; Ly-2; Ly-35; Ly-B; Lyt-2; MAL; T-lymphocyte antigen 2; expressed sequence BB154331; lymphocyte antigen 2; lymphocyte antigen 35; p32; | ||
| Molecular Note | A neomycin resistance gene was inserted into exon 1. Flow cytometry analysis on thymus and lymph node cells derived from homozygous mice confirmed that no detectable encoded protein was expressed on the cell surface. [MGI Ref ID J:68956] [MGI Ref ID J:82297] | ||
Genotyping Protocols
Cd8atm1Mak, Melt Curve Analysis
Cd8atm1Mak, Standard PCR
Generic Cd4, Standard PCR
Helpful Links
Genotyping resources and troubleshooting
Mak TW; Rahemtulla A; Schilham M; Koh DR; Fung-Leung WP. 1992. Generation of mutant mice lacking surface expression of CD4 or CD8 by gene targeting. J Autoimmun 5 Suppl A:55-9. [PubMed: 1503636] [MGI Ref ID J:575]
Fung-Leung WP; Schilham MW; Rahemtulla A; Kundig TM; Vollenweider M; Potter J; van Ewijk W; Mak TW. 1991. CD8 is needed for development of cytotoxic T cells but not helper T cells. Cell 65(3):443-9. [PubMed: 1673361] [MGI Ref ID J:68956]
Rahemtulla A; Fung-Leung WP; Schilham MW; Kundig TM; Sambhara SR; Narendran A; Arabian A; Wakeham A; Paige CJ; Zinkernagel RM; et al.. 1991. Normal development and function of CD8+ cells but markedly decreased helper cell activity in mice lacking CD4. Nature 353(6340):180-4. [PubMed: 1832488] [MGI Ref ID J:68957]
Schilham MW; Fung-Leung WP; Rahemtulla A; Kuendig T; Zhang L; Potter J; Miller RG; Hengartner H; Mak TW. 1993. Alloreactive cytotoxic T cells can develop and function in mice lacking both CD4 and CD8. Eur J Immunol 23(6):1299-304. [PubMed: 8500525] [MGI Ref ID J:12572]
Cd4tm1Mak relatedCd8atm1Mak relatedAdoro S; Erman B; Sarafova SD; Van Laethem F; Park JH; Feigenbaum L; Singer A. 2008. Targeting CD4 coreceptor expression to postselection thymocytes reveals that CD4/CD8 lineage choice is neither error-prone nor stochastic. J Immunol 181(10):6975-83. [PubMed: 18981117] [MGI Ref ID J:140942]
Antony PA; Piccirillo CA; Akpinarli A; Finkelstein SE; Speiss PJ; Surman DR; Palmer DC; Chan CC; Klebanoff CA; Overwijk WW; Rosenberg SA; Restifo NP. 2005. CD8+ T cell immunity against a tumor/self-antigen is augmented by CD4+ T helper cells and hindered by naturally occurring T regulatory cells. J Immunol 174(5):2591-601. [PubMed: 15728465] [MGI Ref ID J:129825]
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Battegay M; Moskophidis D; Rahemtulla A; Hengartner H; Mak TW; Zinkernagel RM. 1994. Enhanced establishment of a virus carrier state in adult CD4+ T-cell-deficient mice. J Virol 68(7):4700-4. [PubMed: 7911534] [MGI Ref ID J:18756]
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Black KE; Murray JA; David CS. 2002. HLA-DQ Determines the Response to Exogenous Wheat Proteins: A Model of Gluten Sensitivity in Transgenic Knockout Mice. J Immunol 169(10):5595-600. [PubMed: 12421937] [MGI Ref ID J:80059]
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Kang TW; Yevsa T; Woller N; Hoenicke L; Wuestefeld T; Dauch D; Hohmeyer A; Gereke M; Rudalska R; Potapova A; Iken M; Vucur M; Weiss S; Heikenwalder M; Khan S; Gil J; Bruder D; Manns M; Schirmacher P; Tacke F; Ott M; Luedde T; Longerich T; Kubicka S; Zender L. 2011. Senescence surveillance of pre-malignant hepatocytes limits liver cancer development. Nature 479(7374):547-51. [PubMed: 22080947] [MGI Ref ID J:179823]
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Kim IS; Baek SH. 2010. Mouse models for breast cancer metastasis. Biochem Biophys Res Commun 394(3):443-7. [PubMed: 20230796] [MGI Ref ID J:159230]
Kish DD; Li X; Fairchild RL. 2009. CD8 T cells producing IL-17 and IFN-gamma initiate the innate immune response required for responses to antigen skin challenge. J Immunol 182(10):5949-59. [PubMed: 19414746] [MGI Ref ID J:148247]
Klein MA; Frigg R; Flechsig E; Raeber AJ; Kalinke U; Bluethmann H; Bootz F; Suter M; Zinkernagel RM; Aguzzi A. 1997. A crucial role for B cells in neuroinvasive scrapie [see comments] Nature 390(6661):687-90. [PubMed: 9414161] [MGI Ref ID J:44933]
Koh DR; Ho A; Rahemtulla A; Fung-Leung WP; Griesser H; Mak TW. 1995. Murine lupus in MRL/lpr mice lacking CD4 or CD8 T cells. Eur J Immunol 25(9):2558-62. [PubMed: 7589126] [MGI Ref ID J:28923]
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Wallace VA; Kondo S; Kono T; Xing Z; Timms E; Furlonger C; Keystone E; Gauldie J; Sauder DN; Mak TW; Paige CJ. 1994. A role for CD4+ T cells in the pathogenesis of skin fibrosis in tight skin mice. Eur J Immunol 24(6):1463-6. [PubMed: 7911425] [MGI Ref ID J:18913]
Wallace VA; Penninger J; Mak TW. 1994. T-Cell development in CD4, CD8, and p56(lck) Gene-Targeted mice.. In: Transgenesis and Targeted Mutagenesis in Immunology. Academic Press, Inc.. [MGI Ref ID J:21662]
Wang B; Fujisawa H; Zhuang L; Freed I; Howell BG; Shahid S; Shivji GM; Mak TW; Sauder DN. 2000. CD4(+) Th1 and CD8(+) type 1 cytotoxic T cells both play a crucial role in the full development of contact hypersensitivity J Immunol 165(12):6783-90. [PubMed: 11120799] [MGI Ref ID J:66170]
Wang T; Chen L; Ahmed E; Ma L; Yin D; Zhou P; Shen J; Xu H; Wang CR; Alegre ML; Chong AS. 2008. Prevention of allograft tolerance by bacterial infection with Listeria monocytogenes. J Immunol 180(9):5991-9. [PubMed: 18424719] [MGI Ref ID J:134678]
Weber SE; Tian H; Pirofski LA. 2011. CD8+ cells enhance resistance to pulmonary serotype 3 Streptococcus pneumoniae infection in mice. J Immunol 186(1):432-42. [PubMed: 21135172] [MGI Ref ID J:168003]
Wei B; Su TT; Dalwadi H; Stephan RP; Fujiwara D; Huang TT; Brewer S; Chen L; Arditi M; Borneman J; Rawlings DJ; Braun J. 2008. Resident enteric microbiota and CD8(+) T cells shape the abundance of marginal zone B cells. Eur J Immunol 38(12):3411-3425. [PubMed: 19009526] [MGI Ref ID J:141389]
Wei B; Wingender G; Fujiwara D; Chen DY; McPherson M; Brewer S; Borneman J; Kronenberg M; Braun J. 2010. Commensal microbiota and CD8+ T cells shape the formation of invariant NKT cells. J Immunol 184(3):1218-26. [PubMed: 20048124] [MGI Ref ID J:159495]
Wen T; Trumper L; Fung-Leung W; Rahemtulla A; Klein E; Klein G; Mak TW. 1998. Requirement of the CD8+ or CD4+ T lymphocyte subsets for the rejection of lymphoma and fibrosarcoma grafts studied in gene knockout hosts. Immunol Lett 61(2-3):187-90. [PubMed: 9657273] [MGI Ref ID J:47925]
Wesche-Soldato DE; Chung CS; Gregory SH; Salazar-Mather TP; Ayala CA; Ayala A. 2007. CD8+ T cells promote inflammation and apoptosis in the liver after sepsis: role of Fas-FasL. Am J Pathol 171(1):87-96. [PubMed: 17591956] [MGI Ref ID J:122836]
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Wolfort RM; Stokes KY; Granger DN. 2008. CD4+ T lymphocytes mediate hypercholesterolemia-induced endothelial dysfunction via a NAD(P)H oxidase-dependent mechanism. Am J Physiol Heart Circ Physiol 294(6):H2619-26. [PubMed: 18408127] [MGI Ref ID J:136828]
Xiang J; Huang H; Liu Y. 2005. A new dynamic model of CD8+ T effector cell responses via CD4+ T helper-antigen-presenting cells. J Immunol 174(12):7497-505. [PubMed: 15944248] [MGI Ref ID J:100792]
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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 |
|
![]() |
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).
|
|
Cryopreserved. Ready for recovery. Please refer to pricing and supply notes for further information.
| Control | ||
|---|---|---|
| 101045 B6129SF2/J | (approximate) | |
| Considerations for Choosing Controls | ||
| Control Pricing Information for Genetically Engineered Mutant Strains. | ||
For Licensing and Use Restrictions view the link(s) below:
- Strain(s) not available to companies or for-profit entities.
| phone: | 207-288-6470 |
| fax: | 207-288-6655 |
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