B6J.B6N(129S7)-Ldlrtm1Her Apobtm2Sgy Tg(Csf1r-EGFP/Rpl10a)1Glass/Oulu

Status

Available to order

EMMA IDEM:15575
Citation informationRRID:IMSR_EM:15575 

Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information.

International strain nameB6J.B6N(129S7)-Ldlrtm1Her Apobtm2Sgy Tg(Csf1r-EGFP/Rpl10a)1Glass/Oulu
Alternative namecfms-EGFP-L10a/Ldlr- ApoB100only
Strain typeTargeted Mutant Strains : Knock-out
Allele/Transgene symbolApobtm2Sgy, Tg(Csf1r-EGFP/Rpl10a)1Glass, Ldlrtm1Her
Gene/Transgene symbolApob, Tg(Csf1r-EGFP/Rpl10a)1Glass, Ldlr

Information from provider

ProviderMinna Kaikkonen-Määttä
Provider affiliationA.I. Virtanen -instituutti, University of Eastern Finland
Additional ownerThe original cfms-L10a-EGFP strain was developed by Prof. Christopher Glass at University of California San Diego. The L10a-EGFP construct was provided by Prof. Nathaniel Heintz, Howard Hughes Medical Institute/The Rockefeller University.
Genetic informationThe construct expressing L10alpha ribosomal subunit (Rpl10a) fused to EGFP was obtained from N. Heintz (Rockfeller U. NY). The EGFP-L10alpha construct was then cloned downstream of the Csf1r (c-fms) promoter (Sasmono et al., Blood 2003, doi:10.1182/blood-2002-02-0569) and the resulting vector injected into the pronuclei of fertilized oocytes. The EGFP-L10alpha fusion protein is constitutively expressed in myeloid cells. The EGFP-L10alpha transgenic mice were crossed to the double-mutant strain for Ldlr and ApoB (The Jackson Laboratory, strain #003000). Expression of EGFP-L10alpha allows to specifically immunoprecipitate polysome bound mRNA in myeloid cells in atherosclerosis diseases.
Phenotypic informationHomozygous:
The expression of EGFPL10alpha allows to specifically immunprecipitate polysome bound mRNA in myeloid cells in atherosclerosis disease.

Heterozygous:
The expression of EGFPL10alpha allows to specifically immunprecipitate polysome bound mRNA in myeloid cells in atherosclerosis disease.
Breeding historyTransgenic mice were generated in the C57BL/6NHsd (code 044) genetic background and have been bred to C57BL/6JOlaHsd since 2013.
References
  • 25-Hydroxycholesterol activates the integrated stress response to reprogram transcription and translation in macrophages.;Shibata Norihito, Carlin Aaron F, Spann Nathanael J, Saijo Kaoru, Morello Christopher S, McDonald Jeffrey G, Romanoski Casey E, Maurya Mano R, Kaikkonen Minna U, Lam Michael T, Crotti Andrea, Reichart Donna, Fox Jesse N, Quehenberger Oswald, Raetz Christian R H, Sullards M Cameron, Murphy Robert C, Merrill Alfred H, Brown H Alex, Dennis Edward A, Fahy Eoin, Subramaniam Shankar, Cavener Douglas R, Spector Deborah H, Russell David W, Glass Christopher K, ;2013;The Journal of biological chemistry;288;35812-23; 24189069
  • Single-cell to pre-clinical evaluation of Trem2, Folr2, and Slc7a7 as macrophage-associated biomarkers for atherosclerosis.;Örd Tiit, Palani Senthil, Giroud Gerbetant Judith, Bodoy Susanna, Lönnberg Tapio, Niskanen Henri, Ravindran Aarthi, Holappa Lari, Chemaly Melody, Taipale Mari, Õunap Kadri, Haikonen Retu, Talukdar Husain, Sukhavasi Katyayani, Liljenbäck Heidi, Virta Jenni, Ruotsalainen Anna-Kaisa, Pierrot-Blanchet Clara, Miner Maxwell W G, Moisio Olli, Rajala Noora, Li Xiang-Guo, Low Philip S, Saraste Antti, Heinäniemi Merja, Ylä-Herttuala Seppo, Björkegren Johan L M, Hedin Ulf, Matic Ljubica, Yvan-Charvet Laurent, Palacín Manuel, Roivainen Anne, Kaikkonen Minna U, ;2025;Cardiovascular research;121;2503-2519; 41206594
Homozygous fertilenot known
Homozygous viablenot known
Homozygous matings requiredno
Immunocompromisedno

Information from EMMA

Archiving centreUniversity of Oulu, Oulu, Finland
Animals used for archivinghomozygous males
Stage of embryos2-cell

Disease and phenotype information

Orphanet associated rare diseases, based on orthologous gene matching

IMPC phenotypes (gene matching)
  • increased circulating cholesterol level / IMPC
  • abnormal auditory brainstem response / IMPC
  • increased mean corpuscular volume / IMPC
  • decreased circulating unsaturated transferrin level / IMPC
  • increased circulating HDL cholesterol level / IMPC
  • increased grip strength / IMPC
  • increased circulating iron level / IMPC
  • abnormal retina blood vessel morphology / IMPC
  • decreased locomotor activity / IMPC
MGI phenotypes (allele matching)
  • increased circulating triglyceride level / MGI
  • increased circulating cholesterol level / MGI
  • hyperglycemia / MGI
  • increased circulating LDL cholesterol level / MGI
  • alopecia / MGI
  • abnormal liver physiology / MGI
  • abnormal adrenal gland morphology / MGI
  • scaly skin / MGI
  • thick skin / MGI
  • increased circulating HDL cholesterol level / MGI
  • hepatic steatosis / MGI
  • decreased circulating triglyceride level / MGI
  • increased cholesterol level / MGI
  • increased circulating VLDL cholesterol level / MGI
  • atherosclerotic lesions / MGI
  • homeostasis/metabolism phenotype / MGI
  • increased liver cholesterol level / MGI
  • abnormal microglial cell morphology / MGI
  • abnormal circulating cholesterol level / MGI
  • decreased circulating HDL cholesterol level / MGI
  • abnormal triglyceride level / MGI
  • abnormal CNS glial cell morphology / MGI
  • hyperactivity / MGI
  • abnormal spatial learning / MGI
  • increased circulating insulin level / MGI
  • abnormal astrocyte morphology / MGI
  • amyloid beta deposits / MGI
  • increased circulating VLDL triglyceride level / MGI
  • impaired glucose tolerance / MGI
  • abnormal fat pad morphology / MGI
  • increased susceptibility to atherosclerosis / MGI
  • increased susceptibility to weight gain / MGI
  • increased percent body fat/body weight / MGI
  • abnormal spatial working memory / MGI
  • increased circulating tumor necrosis factor level / MGI
  • decreased circulating interleukin-10 level / MGI
  • increased circulating interleukin-6 level / MGI
  • increased circulating interleukin-1 beta level / MGI
  • increased liver triglyceride level / MGI
  • increased grip strength / MGI
  • decreased susceptibility to weight gain / MGI
  • abnormal hippocampus morphology / MGI
  • obese / MGI
  • increased circulating free fatty acid level / MGI
  • liver inflammation / MGI
  • abnormal glucose homeostasis / MGI
  • decreased circulating corticosterone level / MGI
  • increased circulating alanine transaminase level / MGI
  • increased liver weight / MGI
  • liver fibrosis / MGI
  • oxidative stress / MGI
  • maternal effect / MGI
  • increased hepatocyte apoptosis / MGI
  • decreased lean body mass / MGI
  • abnormal arteriole morphology / MGI
  • abnormal retinal pigment epithelium morphology / MGI
  • abnormal Bruch membrane morphology / MGI
  • abnormal circulating amino acid level / MGI
  • insulin resistance / MGI
  • increased circulating glucose level / MGI
  • abnormal choriocapillaris morphology / MGI
  • abnormal short term spatial reference memory / MGI
  • abnormal synaptic bouton morphology / MGI
  • photoreceptor outer segment degeneration / MGI
  • abnormal synapse morphology / MGI
  • abnormal circulating LDL cholesterol level / MGI
  • abnormal lipid homeostasis / MGI
  • abnormal cholesterol homeostasis / MGI
  • abnormal circulating protein level / MGI
MGI phenotypes (gene matching)
  • abnormal microglial cell morphology / MGI
  • abnormal circulating cholesterol level / MGI
  • abnormal circulating LDL cholesterol level / MGI
  • increased circulating LDL cholesterol level / MGI
  • decreased circulating HDL cholesterol level / MGI
  • abnormal triglyceride level / MGI
  • alopecia / MGI
  • abnormal liver physiology / MGI
  • abnormal adrenal gland morphology / MGI
  • abnormal hippocampus morphology / MGI
  • abnormal CNS glial cell morphology / MGI
  • scaly skin / MGI
  • thick skin / MGI
  • obese / MGI
  • hyperactivity / MGI
  • abnormal spatial learning / MGI
  • increased circulating triglyceride level / MGI
  • increased circulating free fatty acid level / MGI
  • increased circulating HDL cholesterol level / MGI
  • hyperglycemia / MGI
  • liver inflammation / MGI
  • abnormal glucose homeostasis / MGI
  • increased circulating insulin level / MGI
  • abnormal lipid homeostasis / MGI
  • no abnormal phenotype detected / MGI
  • abnormal astrocyte morphology / MGI
  • hepatic steatosis / MGI
  • decreased circulating triglyceride level / MGI
  • decreased circulating corticosterone level / MGI
  • gallstones / MGI
  • increased circulating alanine transaminase level / MGI
  • increased liver weight / MGI
  • no phenotypic analysis / MGI
  • retinal detachment / MGI
  • amyloid beta deposits / MGI
  • liver fibrosis / MGI
  • oxidative stress / MGI
  • maternal effect / MGI
  • increased hepatocyte apoptosis / MGI
  • abnormal circulating lipid level / MGI
  • decreased lean body mass / MGI
  • increased circulating VLDL triglyceride level / MGI
  • increased cholesterol level / MGI
  • abnormal arteriole morphology / MGI
  • increased macrophage derived foam cell number / MGI
  • increased circulating VLDL cholesterol level / MGI
  • increased circulating cholesterol level / MGI
  • decreased circulating cholesterol level / MGI
  • abnormal retinal pigment epithelium morphology / MGI
  • abnormal Bruch membrane morphology / MGI
  • abnormal cholesterol homeostasis / MGI
  • impaired glucose tolerance / MGI
  • abnormal circulating amino acid level / MGI
  • insulin resistance / MGI
  • abnormal fat pad morphology / MGI
  • atherosclerotic lesions / MGI
  • increased susceptibility to atherosclerosis / MGI
  • homeostasis/metabolism phenotype / MGI
  • abnormal circulating protein level / MGI
  • increased susceptibility to weight gain / MGI
  • increased percent body fat/body weight / MGI
  • increased circulating glucose level / MGI
  • abnormal choriocapillaris morphology / MGI
  • abnormal spatial working memory / MGI
  • abnormal short term spatial reference memory / MGI
  • increased circulating tumor necrosis factor level / MGI
  • abnormal synaptic bouton morphology / MGI
  • photoreceptor outer segment degeneration / MGI
  • decreased circulating interleukin-10 level / MGI
  • increased circulating interleukin-6 level / MGI
  • increased circulating interleukin-1 beta level / MGI
  • increased liver triglyceride level / MGI
  • abnormal synapse morphology / MGI
  • increased liver cholesterol level / MGI
  • increased grip strength / MGI
  • decreased susceptibility to weight gain / MGI

Literature references

  • 25-Hydroxycholesterol activates the integrated stress response to reprogram transcription and translation in macrophages.;Shibata Norihito, Carlin Aaron F, Spann Nathanael J, Saijo Kaoru, Morello Christopher S, McDonald Jeffrey G, Romanoski Casey E, Maurya Mano R, Kaikkonen Minna U, Lam Michael T, Crotti Andrea, Reichart Donna, Fox Jesse N, Quehenberger Oswald, Raetz Christian R H, Sullards M Cameron, Murphy Robert C, Merrill Alfred H, Brown H Alex, Dennis Edward A, Fahy Eoin, Subramaniam Shankar, Cavener Douglas R, Spector Deborah H, Russell David W, Glass Christopher K, ;2013;The Journal of biological chemistry;288;35812-23; 24189069
  • Single-cell to pre-clinical evaluation of Trem2, Folr2, and Slc7a7 as macrophage-associated biomarkers for atherosclerosis.;Örd Tiit, Palani Senthil, Giroud Gerbetant Judith, Bodoy Susanna, Lönnberg Tapio, Niskanen Henri, Ravindran Aarthi, Holappa Lari, Chemaly Melody, Taipale Mari, Õunap Kadri, Haikonen Retu, Talukdar Husain, Sukhavasi Katyayani, Liljenbäck Heidi, Virta Jenni, Ruotsalainen Anna-Kaisa, Pierrot-Blanchet Clara, Miner Maxwell W G, Moisio Olli, Rajala Noora, Li Xiang-Guo, Low Philip S, Saraste Antti, Heinäniemi Merja, Ylä-Herttuala Seppo, Björkegren Johan L M, Hedin Ulf, Matic Ljubica, Yvan-Charvet Laurent, Palacín Manuel, Roivainen Anne, Kaikkonen Minna U, ;2025;Cardiovascular research;121;2503-2519; 41206594

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