Overview

CTL and NK cells from mice homozygous for this targeted mutation of Prf1, perforin 1 (pore forming protein), have impaired pathogen clearance. This mutant mouse strain may be useful in studies of inflammatory response, susceptibility to infection, and susceptibility to multiple sclerosis.

Donating Investigator

IMR Colony, The Jackson Laboratory

Genetic overview

Genetic Background	Generation

Prf1^tm1Sdz

Allele Type	Gene Symbol	Gene Name
Targeted (Null/Knockout)	Prf1	perforin 1 (pore forming protein)

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Research Applications

Apoptosis Research
Immunology, Inflammation and Autoimmunity Research
Research Tools

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Base Price

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$2,854.50 Domestic price Cryo Recovery

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Details

Detailed Description

Mice homozygous for the targeted mutation are viable and fertile. Homozygous mutant mice have normal numbers of CD8⁺ T cells and NK cells. CTL and NK cells are unable to lyse virus-infected or allogeneic fibroblasts in vitro. Homozygotes fail to clear lymphocytic choriomeningitis virus. Fibrosarcoma tumor cells are eliminated with reduced efficiency. This mutant mouse strain may be useful in studies of inflammatory response, susceptibility to infection, and susceptibility to multiple sclerosis.

In an attempt to offer alleles on well-characterized or multiple genetic backgrounds, alleles are frequently moved to a genetic background different from that on which an allele was first characterized. This is the case for the strain above. It should be noted that the phenotype could vary from that originally described. We will modify the strain description if necessary as published results become available.

Development

A replacement vector was used containing the neo gene and which resulted in the disruption of exon 3 of the perforin gene without delection of coding sequence. No fully function perforin mRNA was detected by reverse transcription PCR. Male BL/6-III ES cells were used. There cells were originally derived from C57BL/6 mice. The mice were then backcrossed five generations with BALB/cByJ inbred mice (Stock No. 001026).

Control Suggestions

001026 BALB/cByJ

Additional Information

Considerations for Choosing Controls

Selected References

Kagi D; Ledermann B; Burki K; Seiler P; Odermatt B; Olsen KJ; Podack ER; Zinkernagel RM; Hengartner H. 1994. Cytotoxicity mediated by T cells and natural killer cells is greatly impaired in perforin-deficient mice [see comments] Nature 369(6475):31-7PubMed: 8164737 MGI: J:17986

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Genetics

Prf1^tm1Sdz

Allele Symbol: Prf1^tm1Sdz

Allele Name	targeted mutation 1, Sandoz Pharmaceuticals
Allele Type	Targeted (Null/Knockout)
Allele Synonym(s)	Prf1^tm1Sdz; targeted mutation 1, Sandoz Pharmaceuticals
Gene Symbol and Name	Prf1, perforin 1 (pore forming protein)
Gene Synonym(s)	Pfp; HPLH2; pore forming protein; Prf-1; perforin; Prf-1; P1; PFP; Pfn; perforin 1; Cyta; RATCYTA; Pfp
Strain of Origin	C57BL/6J
Chromosome	10
Molecular Note	A neomycin selection cassette was inserted into exon 3. RT-PCR analysis on RNA derived from homozygous mice demonstrated that an abnormal transcript was produced from this allele. However, immunocytochemistry experiments on activated spleen cells derived from homozygous mice confirmed that no detectable protein was made from this allele.
Mutations Made By	Dr. Birgit Lederman, University of Zurich

Disease/Phenotype

Disease Terms

Model with phenotypic similarity to human disease where etiologies involve orthologs. Human genes are associated with this disease. Orthologs of those genes appear in the mouse genotype(s).

familial hemophagocytic lymphohistiocytosis 2

Model with phenotypic similarity to human disease where etiologies are distinct. Human genes are associated with this disease. Orthologs of these genes do not appear in the mouse genotype(s).

multiple sclerosis

Research Areas By Genotype

This mouse can be used to support research in many areas including:

Genotype: Prf1^tm1Sdz related

Apoptosis Research
- Extracellular Modulators
Immunology, Inflammation and Autoimmunity Research
- Immunodeficiency Associated with Other Defects

Immunology, Inflammation and Autoimmunity Research
- Immunodeficiency Associated with Other Defects
- Immunodeficiency
  - NK Cell and Cd8 T Cell defects
  - perforin
Apoptosis Research
- Extracellular Modulators
Research Tools
- Apoptosis Research

Mammalian Phenotype Terms by Genotype

The following phenotype information is associated with a similar, but not exact match to this JAX^® Mice strain

Genotype: Prf1^tm1Sdz/Prf1^tm1Sdz
C57BL/6-Prf1

hematopoietic system phenotype

abnormal leukocyte physiology

abnormal NK cell physiology
- impaired ability to clear injected MHC class-I deficient B cell lymphoma cells resulting in increased mortality

decreased cytotoxic T cell cytolysis
- CD8+ T cells cannot lyse in vitro virus-infected, peptide-coated or allogeneic target cells of epithelial, neuroectodermal or mesodermal orgin, however activation and expansion of CD8+ T cells occurs normally

impaired natural killer cell mediated cytotoxicity
- NK-cell-mediated lysis is not evident in the spleen cells after viral infection

mortality/aging

increased sensitivity to induced morbidity/mortality
- all mice die between 40 and 60 days after injection of 10^7 MHC class-I deficient B cell lymphoma cells, while all wild-type mice survive

premature death
- Background Sensitivity - in mice on a C57BL/6 background compared to mice on a BALB/c background

neoplasm

decreased tumor latency
- Background Sensitivity - in mice on a C57BL/6 background compared to mice on a BALB/c background

increased B cell derived lymphoma incidence
- lymphomas are of a B cell origin or plasmocytomas

increased lymphoma incidence
- develop aggressive disseminated lymphomas that affect the spleen, liver and lymph nodes from 300 days of age onwards
- most lymphomas are diffuse large cell lymphomas

reproductive system phenotype

abnormal female reproductive system physiology
- alpha-galactosylceramide induced abortion does not occur

immune system phenotype

abnormal inflammatory response
- fail to develop footpad swelling upon lymphocytic choriomeningitis virus injection into the footpad

abnormal leukocyte physiology

abnormal NK cell physiology
- impaired ability to clear injected MHC class-I deficient B cell lymphoma cells resulting in increased mortality

decreased cytotoxic T cell cytolysis
- CD8+ T cells cannot lyse in vitro virus-infected, peptide-coated or allogeneic target cells of epithelial, neuroectodermal or mesodermal orgin, however activation and expansion of CD8+ T cells occurs normally

impaired natural killer cell mediated cytotoxicity
- NK-cell-mediated lysis is not evident in the spleen cells after viral infection

increased interleukin-10 secretion
- following infection with a monocytotropic Ehrlichia bacteria from Ixodes ovatrus ticks (IOE), IL-10 production is increased relative to infected wild-type mice

increased susceptibility to bacterial infection
- f contiguous hepatocytes with mild to moderate liver injury, and more macrophage-rich inflammatory infiltrates compared to infected wild-type mice
- following infection with a monocytotropic Ehrlichia bacteria from Ixodes ovatrus ticks (IOE), mice have a higher burden of bacteria in the liver and lungs but not spleens, develop extensive partially confluent foci of apoptosis or necrosis of contiguous hepatocytes with mild to moderate liver injury, and more macrophage-rich inflammatory infiltrates compared to infected wild-type mice
- following infection with IOE, IL-10 production is increased relative to infected wild-type mice

increased susceptibility to infection

increased susceptibility to parasitic infection
- decreased clearance and survival after infection with Trypanosoma cruzi

increased susceptibility to viral infection
- unable to eliminate lymphocytic choriomeningitis virus 12 days after intravenous infection as in controls, with infection eventually leading to weight loss and death between days 13 and 16

Genotype: Prf1^tm1Sdz/Prf1^tm1Sdz
C57BL/6-Prf1/J

behavior/neurological phenotype

abnormal behavior
- some chronically infected mice demonstrate minor alterations in stride with normal activity levels, despite presence of demyelination

hunched posture
- in LMCV-infected mice
- mutants infected with LCMV display hunched posture 10 days after infection unlike wild-type mice

hypoactivity
- mutants infected with lymphocytic choriomeningitic virus (LCMV) display decreased activity 10 days after infection compared with wild-type controls

lethargy
- in LMCV-infected mice

nervous system phenotype

abnormal brain meninges morphology
- 30 days after LCMV infection, the meninges show prominent mononuclear infiltrates along the dura

brain inflammation
- 30 days after LCMV infection, the meninges show prominent mononuclear infiltrates along the dura
- at 180 days, brain pathology is still present
- by 45 days, inflammation with parenchymal disease is seen in hippocampus, striatum, and corpus callosum in some mice
- by 7 days after TMEV infection, inflammation is present, decreasing slightly by 21 days, but widespread tissue damage is present, similar to controls (B6)
- persistent inflammation is found in the brainstem of mutants

CNS inflammation
- by 21 days, inflammation with macrophage infiltration persists in the gray matter in mutants but not in controls
- by 7 days after TMEV infection, inflammation is present in the meninges and gray matter of spinal cords in controls as well

demyelination
- at 45 days after infection, foci of demyelination are observed in spinal cord (in 11% of 537 quadrants examined)
- demyelinated axons in close proximity to inflammatory cells and macrophages with intracytoplasmic vacuoles containing myelin debris are seen in mutants, but not in control or other null mice
- lesions are located mainly in the anterior and anterolateral white matter of the spinal cord; demyelination is chronic and progressive (16% of quadrants at 90 days and 20% of quadrants at 180 days)

homeostasis/metabolism phenotype

abnormal body temperature homeostasis
- while wild-type mice infected with LCMV develop a brief febrile response early after infection, mutants exhibit a prolonged temperature elevation that is still seen at 10 days after infection

abnormal circulating cytokine level

abnormal circulating fibrinogen level
- 8-10 days after LCMV infection, mutants develop hypofibrinogenemia compared to wild-type controls

decreased body temperature
- in LMCV-infected mice

increased circulating aspartate transaminase level
- in LMCV-infected mice

increased circulating interferon-alpha level
- mutants exhibit elevated serum levels of IFN-alpha at 6-8 days after LCMV infection unlike wild-type mice which show peak IFN-alpha levels at day 3 of infection and undetectable levels by 4-5 days of infection

increased circulating interferon-gamma level
- in LMCV-infected mice
- mutants exhibit elevated (10- to 100-fold) and prolonged serum levels of IFN-gamma following LCMV infection compared to wild-type mice
- mutants treated with neutralizing antibodies against IFN-gamma survive LCMV infection, do not develop histocytic infiltrates or peripheral blood cytopenias

increased circulating interleukin-1 beta level
- in LMCV-infected mice

increased circulating interleukin-10 level
- increased at 12 days after LCMV infection compared to wild-type mice

increased circulating interleukin-18 level
- increased at 12 days after LCMV infection compared to wild-type mice

increased circulating interleukin-6 level
- in LMCV-infected mice
- increased at 12 days after LCMV infection compared to wild-type mice

increased circulating lactate dehydrogenase level
- in LMCV-infected mice

increased circulating triglyceride level
- 8-10 days after LCMV infection, mutants develop hypertriglyceridemia compared to wild-type controls

increased circulating tumor necrosis factor level
- in LMCV-infected mice
- increased at 12 days after LCMV infection compared to wild-type mice

immune system phenotype

abnormal circulating cytokine level

abnormal circulating fibrinogen level
- 8-10 days after LCMV infection, mutants develop hypofibrinogenemia compared to wild-type controls

abnormal cytotoxic T cell physiology
- Normal - however, priming is normal
- impaired CD8+ T cell degranulation

abnormal lymph node morphology
- by 10-12 days after LCMV infection, lymph node architecture is deranged with disorganized macrophage and activated lymphocyte infiltrates replacing the normal follicular structure of lymph nodes and some lymph nodes exhibit necrotic changes compared to wild-type mice
- ld-type mice

abnormal lymphocyte physiology
- CNS-infiltrating mononuclear cells have impaired lytic activity LP- and VP2-transfected target cells in vitro (TMEV leader peptide and VP2 capsid protein), in contrast to effective lysis demonstrated by control cells

abnormal macrophage activation involved in immune response
- hemophagocytic macrophages are seen in lymph node, spleen, liver and bone marrow tissues of LCMV infected mutants unlike in wild-type mice

abnormal spleen white pulp morphology
- by 10-12 days after LCMV infection, the white pulp appears chaotic with a prominent infiltrate of macrophages and activated lymphocytes when compared to wild-type spleen

abnormal T cell activation
- mutants exhibit an elevation of antigen-specific CD8+ T and CD4+ T cells in the bone marrow, liver, and spleen following LCMV infection compared to wild-type mice

brain inflammation
- 30 days after LCMV infection, the meninges show prominent mononuclear infiltrates along the dura
- at 180 days, brain pathology is still present
- by 45 days, inflammation with parenchymal disease is seen in hippocampus, striatum, and corpus callosum in some mice
- by 7 days after TMEV infection, inflammation is present, decreasing slightly by 21 days, but widespread tissue damage is present, similar to controls (B6)
- persistent inflammation is found in the brainstem of mutants

CNS inflammation
- by 21 days, inflammation with macrophage infiltration persists in the gray matter in mutants but not in controls
- by 7 days after TMEV infection, inflammation is present in the meninges and gray matter of spinal cords in controls as well

decreased cytotoxic T cell cytolysis
- 2Ics cells
- reduced killing of anti-CD3-loaded P815 target cells, more pronounced than in than in Rab27a^ash and Stx11^tm1.2Ics cells

decreased interferon-gamma secretion
- ells is increased, indicating that ongoing antigenic stimulation results in the increased cytokine secretion
- IFN-gamma production by CD8+ T cells is less on a per-cell basis in response to both peptide and anti-CD3 stimulation after LCMV infection compared with wild-type mice, however the number of spontaneously IFN-gamma producing (without stimulation) CD8+ T cells is increased, indicating that ongoing antigenic stimulation results in the increased cytokine secretion

decreased leukocyte cell number
- in LMCV-infected mice

decreased neutrophil cell number
- lack of neutrophilia in LMCV-infected mice

decreased NK cell degranulation
- in the presence of recombinant IL15 alone or in combination with IL2

increased circulating interferon-alpha level
- mutants exhibit elevated serum levels of IFN-alpha at 6-8 days after LCMV infection unlike wild-type mice which show peak IFN-alpha levels at day 3 of infection and undetectable levels by 4-5 days of infection

increased circulating interferon-gamma level
- in LMCV-infected mice
- mutants exhibit elevated (10- to 100-fold) and prolonged serum levels of IFN-gamma following LCMV infection compared to wild-type mice
- mutants treated with neutralizing antibodies against IFN-gamma survive LCMV infection, do not develop histocytic infiltrates or peripheral blood cytopenias

increased circulating interleukin-1 beta level
- in LMCV-infected mice

increased circulating interleukin-10 level
- increased at 12 days after LCMV infection compared to wild-type mice

increased circulating interleukin-18 level
- increased at 12 days after LCMV infection compared to wild-type mice

increased circulating interleukin-6 level
- in LMCV-infected mice
- increased at 12 days after LCMV infection compared to wild-type mice

increased circulating tumor necrosis factor level
- in LMCV-infected mice
- increased at 12 days after LCMV infection compared to wild-type mice

increased spleen red pulp amount
- by 10-12 days after LCMV infection, red pulp is expanded when compared to wild-type mice

increased susceptibility to viral infection
- homozygotes despite similar viral loads
- at 45 days, viral mRNA is still detected in spinal cords of mutants but not in controls or Fas and Fasl mutants
- inflammation and tissue damage in the brain are greater than in control, resistant mice at 45 and 180 days
- irculating lactate dehydrogenase level, increased serum levels of IFN-gamma, IL1b, TNF-alpha and IL6, increased viral load and worsening condition compared with wild-type mice
- LMCV-infected mice develop clinical features of hemophagocytic lymphohistiocytosis including weight loss, body temperature drop, hunched posture, lethargy, pancytopenia, lack of neutrophilia, increased circulating aspartate transaminase level, increased circulating lactate dehydrogenase level, increased serum levels of IFN-gamma, IL1b, TNF-alpha and IL6, increased viral load and worsening condition compared with wild-type mice
- LMCV-infected mice develop more severe hemophagocytic lymphohistiocytosis than in Rab27a^ash and Stx11^tm1.2Ics homozygotes despite similar viral loads
- mutants cannot clear lymphocytic choriomeningitic virus (LCMV) infection like wild-type mice can

increased susceptibility to viral infection induced morbidity/mortality
- mice die 2 weeks after LCMV infection
- mutants depleted of CD8+ cells (by administration of antibodies against CD8+ cells) survive LCMV infection, however those depleted of CD4+ or NK cells do not survive
- mutants die within 2 weeks of lymphocytic choriomeningitic virus (LCMV) infection unlike wild-type mice
- mutants treated with neutralizing antibodies against IFN-gamma survive LCMV infection, do not develop histocytic infiltrates or peripheral blood cytopenias
- neutralizing multiple cytokines, including TNF-alpha, IL-12, IL-18, M-CSF, and GM-CSF, with neutralizing antibodies has no effect on survival

liver inflammation
- by 10-12 days after LCMV infection, livers show prominent periportal infiltrates

lymph node inflammation
- by 10-12 days after LCMV infection, lymph node architecture is deranged with disorganized macrophage and activated lymphocyte infiltrates replacing the normal follicular structure

growth/size/body region phenotype

weight loss
- in LMCV-infected mice

hematopoietic system phenotype

abnormal cytotoxic T cell physiology
- Normal - however, priming is normal
- impaired CD8+ T cell degranulation

abnormal lymphocyte physiology
- CNS-infiltrating mononuclear cells have impaired lytic activity LP- and VP2-transfected target cells in vitro (TMEV leader peptide and VP2 capsid protein), in contrast to effective lysis demonstrated by control cells

abnormal macrophage activation involved in immune response
- hemophagocytic macrophages are seen in lymph node, spleen, liver and bone marrow tissues of LCMV infected mutants unlike in wild-type mice

abnormal spleen white pulp morphology
- by 10-12 days after LCMV infection, the white pulp appears chaotic with a prominent infiltrate of macrophages and activated lymphocytes when compared to wild-type spleen

abnormal T cell activation
- mutants exhibit an elevation of antigen-specific CD8+ T and CD4+ T cells in the bone marrow, liver, and spleen following LCMV infection compared to wild-type mice

decreased bone marrow cell number
- bone marrow shows severe hypoplasia by 10-12 days after LCMV infection when compared to wild-type mice

decreased cytotoxic T cell cytolysis
- 2Ics cells
- reduced killing of anti-CD3-loaded P815 target cells, more pronounced than in than in Rab27a^ash and Stx11^tm1.2Ics cells

decreased erythrocyte cell number
- in LMCV-infected mice

decreased leukocyte cell number
- in LMCV-infected mice

decreased neutrophil cell number
- lack of neutrophilia in LMCV-infected mice

decreased NK cell degranulation
- in the presence of recombinant IL15 alone or in combination with IL2

increased spleen red pulp amount
- by 10-12 days after LCMV infection, red pulp is expanded when compared to wild-type mice

pancytopenia
- in LMCV-infected mice
- unlike wild-type mice, mutants become pancytopenic by 10 days after LCMV infection

thrombocytopenia
- in LMCV-infected mice

integument phenotype

ruffled hair
- mutants infected with LCMV display ruffled fur 10 days after infection when compared with wild-type controls

liver/biliary system phenotype

liver inflammation
- by 10-12 days after LCMV infection, livers show prominent periportal infiltrates

mammalian phenotype

behavior/neurological phenotype
- e at 90 days and 64% by 180 days
- mice infected with TMEV and monitored daily do not show clinical signs of TMEV infecion, including unkempt appearance, decreased spontaneous movement and hind-limb paralysis, at 45 days and 90 days, whereas 12% of susceptible SJL mice show clinical disease at 90 days and 64% by 180 days

immune system phenotype
- delayed type hypersensitivity (DTH) reaction elicited in the ear by intradermal injection of inactive virus is comparable to that of controls

mortality/aging

increased susceptibility to viral infection induced morbidity/mortality
- mice die 2 weeks after LCMV infection
- mutants depleted of CD8+ cells (by administration of antibodies against CD8+ cells) survive LCMV infection, however those depleted of CD4+ or NK cells do not survive
- mutants die within 2 weeks of lymphocytic choriomeningitic virus (LCMV) infection unlike wild-type mice
- mutants treated with neutralizing antibodies against IFN-gamma survive LCMV infection, do not develop histocytic infiltrates or peripheral blood cytopenias
- neutralizing multiple cytokines, including TNF-alpha, IL-12, IL-18, M-CSF, and GM-CSF, with neutralizing antibodies has no effect on survival

Genotype: Prf1^tm1Sdz/Prf1^tm1Sdz
involves: BALB/c * C57BL/6

hematopoietic system phenotype

impaired natural killer cell mediated cytotoxicity
- activated splenic NK cells are unable to kill 4T1 or Renca tumor target cells

immune system phenotype

impaired natural killer cell mediated cytotoxicity
- activated splenic NK cells are unable to kill 4T1 or Renca tumor target cells

Genotype: Prf1^tm1Sdz/Prf1^tm1Sdz
A.B6-Prf1

hematopoietic system phenotype

impaired natural killer cell mediated cytotoxicity
- A cytotoxicity assay based on flow cytometric analysis of the number of doubly-labeled NK cell-sensitive Yac-1 target cells that had been labeled with CFSE before and with 7-ADD after incubation with fresh spleen cells demonstrated significantly reduced cytolysis by homozygous mutant vs. wild-type A/J NK cells. (n = 3/genotype; P = 0.0031. Student's t test.)
- ytolysis by homozygous mutant vs. wild-type A/J NK cells. (n = 3/genotype; P = 0.0031. Student's t test.)

immune system phenotype

impaired natural killer cell mediated cytotoxicity
- A cytotoxicity assay based on flow cytometric analysis of the number of doubly-labeled NK cell-sensitive Yac-1 target cells that had been labeled with CFSE before and with 7-ADD after incubation with fresh spleen cells demonstrated significantly reduced cytolysis by homozygous mutant vs. wild-type A/J NK cells. (n = 3/genotype; P = 0.0031. Student's t test.)
- ytolysis by homozygous mutant vs. wild-type A/J NK cells. (n = 3/genotype; P = 0.0031. Student's t test.)

neoplasm

increased incidence of induced tumors
- Normal - 0.16)
- Normal - although a significantly greater tumor volume was observed in NKK-treated heterozygous mutant female mice than in wild-type mice (P = 0.034), the volume of tumors in homozygous mutant mice did not differ significantly from that in wild-type controls (P = 0.16)
- ce (wt n= 17, homozygous n = 26; P = 0.036. Mann-Whitney U test.)
- homozygous mutant female A/J mice treated at 6 weeks of age with 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NKK) had developed a significantly greater number of lung adenomas/adenocarcinomas 22 weeks later than had NKK-treated wild-type female A/J mice (wt n= 17, homozygous n = 26; P = 0.036. Mann-Whitney U test.)

Genotype: Prf1^tm1Sdz/Prf1⁺
A.B6-Prf1

hematopoietic system phenotype

impaired natural killer cell mediated cytotoxicity
- A cytotoxicity assay based on flow cytometric analysis of the number of doubly-labeled NK cell-sensitive Yac-1 target cells that had been labeled with CFSE before and with 7-ADD after incubation with fresh spleen cells demonstrated significantly reduced cytolysis by heterozygous mutant vs. wild-type A/J NK cells (n = 3/genotype; P = 0.0046. Student's t test.)
- ytolysis by heterozygous mutant vs. wild-type A/J NK cells (n = 3/genotype; P = 0.0046. Student's t test.)

immune system phenotype

impaired natural killer cell mediated cytotoxicity
- A cytotoxicity assay based on flow cytometric analysis of the number of doubly-labeled NK cell-sensitive Yac-1 target cells that had been labeled with CFSE before and with 7-ADD after incubation with fresh spleen cells demonstrated significantly reduced cytolysis by heterozygous mutant vs. wild-type A/J NK cells (n = 3/genotype; P = 0.0046. Student's t test.)
- ytolysis by heterozygous mutant vs. wild-type A/J NK cells (n = 3/genotype; P = 0.0046. Student's t test.)

neoplasm

increased incidence of induced tumors
- 17, heterozygous n = 42; P = 0.031. Mann-Whitney U test.)
- a significantly greater tumor volume was observed in the NKK-treated heterozygous mutant mice than in the NKK-treated wild-type control mice (P = 0.034)
- heterozygous mutant female A/J mice treated at 6 weeks of age with 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NKK) had developed a significantly greater number of lung adenomas/adenocarcinomas 22 weeks later than NKK-treated wild-type A/J mice (wt n= 17, heterozygous n = 42; P = 0.031. Mann-Whitney U test.)

The following phenotype relates to a compound genotype created using this strain

Genotype: Prf1^tm1Sdz/Prf1^tm1Sdz
C.B6-Prf1

endocrine/exocrine gland phenotype

increased T cell derived lymphoma incidence
- in a few mice

neoplasm

abnormal tumor morphology
- some lymphomas have an unusual histiocytic appearance with a pale eosinophilic cytoplasm

increased lung adenocarcinoma incidence
- all are well differentiated papillary adenocarcinomas
- in a few mice, with a very late onset

increased lymphoma incidence
- some mice develop disseminated lymphomas

increased sarcoma incidence
- in a few mice

increased T cell derived lymphoma incidence
- in a few mice

increased tumor latency
- in mice on a BALB/c background compared to mice on a C57BL/6 background

respiratory system phenotype

increased lung adenocarcinoma incidence
- all are well differentiated papillary adenocarcinomas
- in a few mice, with a very late onset

References

Kagi D; Ledermann B; Burki K; Seiler P; Odermatt B; Olsen KJ; Podack ER; Zinkernagel RM; Hengartner H. 1994. Cytotoxicity mediated by T cells and natural killer cells is greatly impaired in perforin-deficient mice [see comments] Nature 369(6475):31-7PubMed: 8164737 MGI: J:17986

Additional - Prf1^tm1Sdz related

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Genotyping Protocols
- Standard PCR: Prf1^tm1Sdz
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When maintaining a live colony, these mice may be bred as homozygotes.
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Citation
When using the CByJ.B6-Prf1^tm1Sdz/J mouse strain in a publication, please cite the originating article(s) and include JAX stock #007079 in your Materials and Methods section.

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Pricing & Availability

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Cryorecovery - Pricing

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	Heterozygous for Prf1<tm1Sdz>

We will fulfill your order by providing at least two carriers for each strain ordered. The total number, sex, and genotypes provided will vary, although typically 8 or more animals are provided. Please check genotypes which will be recovered. While the genotypes of all animals produced will be communicated to you prior to scheduling shipment, the genotypes of animals provided may not reflect the mating scheme and genotypes described in the strain description. Animals are typically ready to ship in 11-14 weeks. If a second recovery is required to produce the minimum number of animals, then delivery time would increase to approximately 25 weeks. If we fail to produce animals of the correct genotype, you will not be charged. We 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.

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In no event shall JACKSON, its trustees, directors, officers, employees, and affiliates be liable for any causes of action or damages, including any direct, indirect, special, or consequential damages, arising out of the provision of MICE, PRODUCTS, or SERVICES, including economic damage or injury to property and lost profits, and including any damage arising from acts or negligence on the part of JACKSON, its agents or employees. Unless prohibited by law, in purchasing or receiving MICE, PRODUCTS, or SERVICES from JACKSON, purchaser or recipient, or any party claiming by or through them, expressly releases and discharges JACKSON from all such causes of action or damages, and further agrees to defend and indemnify JACKSON from any costs or damages arising out of any third party claims.

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Donating Investigator

Genetic overview

Research Applications

Base Price

Detailed Description

Development

Control Suggestions

Additional Information

Selected References

Prf1tm1Sdz

Allele Symbol: Prf1tm1Sdz

Disease Terms

Model with phenotypic similarity to human disease where etiologies involve orthologs. Human genes are associated with this disease. Orthologs of those genes appear in the mouse genotype(s).

Model with phenotypic similarity to human disease where etiologies are distinct. Human genes are associated with this disease. Orthologs of these genes do not appear in the mouse genotype(s).

Research Areas By Genotype

This mouse can be used to support research in many areas including:

Genotype: Prf1tm1Sdz related

Mammalian Phenotype Terms by Genotype

Genotype: Prf1tm1Sdz/Prf1tm1SdzC57BL/6-Prf1

hematopoietic system phenotype

mortality/aging

neoplasm

reproductive system phenotype

immune system phenotype

Genotype: Prf1tm1Sdz/Prf1tm1SdzC57BL/6-Prf1/J

behavior/neurological phenotype

nervous system phenotype

homeostasis/metabolism phenotype

immune system phenotype

growth/size/body region phenotype

hematopoietic system phenotype

integument phenotype

liver/biliary system phenotype

mammalian phenotype

mortality/aging

Genotype: Prf1tm1Sdz/Prf1tm1Sdzinvolves: BALB/c * C57BL/6

hematopoietic system phenotype

immune system phenotype

Genotype: Prf1tm1Sdz/Prf1tm1SdzA.B6-Prf1

hematopoietic system phenotype

immune system phenotype

neoplasm

Genotype: Prf1tm1Sdz/Prf1+A.B6-Prf1

hematopoietic system phenotype

immune system phenotype

neoplasm

Genotype: Prf1tm1Sdz/Prf1tm1SdzC.B6-Prf1

endocrine/exocrine gland phenotype

neoplasm

respiratory system phenotype

References

Additional - Prf1tm1Sdz related

Genotyping Protocols

Breeding Considerations

Citation

Animal Health Reports

Production of mice from cryopreserved embryos or sperm occurs in a maximum barrier room, G200

Live Mouse

Cryorecovery - Pricing

Related Products and Services

Payment Terms and Conditions

The Jackson Laboratory's Genotype Promise

Terms of Use

Licensing Information

JAX® Mice, Products & Services Conditions of Use

No Warranty

Credit for PRODUCTS or SERVICES

Animal Care and Use for SERVICES

No Liability

Prf1^tm1Sdz

Allele Symbol: Prf1^tm1Sdz

Genotype: Prf1^tm1Sdz related

Genotype: Prf1^tm1Sdz/Prf1^tm1Sdz
C57BL/6-Prf1

Genotype: Prf1^tm1Sdz/Prf1^tm1Sdz
C57BL/6-Prf1/J

Genotype: Prf1^tm1Sdz/Prf1^tm1Sdz
involves: BALB/c * C57BL/6

Genotype: Prf1^tm1Sdz/Prf1^tm1Sdz
A.B6-Prf1

Genotype: Prf1^tm1Sdz/Prf1⁺
A.B6-Prf1

Genotype: Prf1^tm1Sdz/Prf1^tm1Sdz
C.B6-Prf1

Additional - Prf1^tm1Sdz related