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Cre Driver Mice Targeting Macrophages
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The efficiency of loxP-mediated gene recombination driven by LysM-Cre varies markedly among myeloid cell types, with the highest efficiency in mature macrophages (approximately 83-98%) and much lower efficiency in splenic DCs (about 16%).
“It is important to note that the efficiency of loxP-mediated gene recombination driven by LysM-Cre varies markedly among myeloid cell types63–65. with the highest efficiency observed in mature macrophages (approximately 83–98%) and much lower efficiency in splenic DCs (about 16%)44.”
From Macrophage INSIG1 deficiency drives psoriasiform dermatitis via the SREBP2-STAT1 axis (2026) · cites this paper as [63]
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Fate Mapping Reveals Origins and Dynamics of Monocytes and Tissue Macrophages under Homeostasis
Yona, S., Kim, K.-W., Wolf, Y., Mildner, A., Varol, D., Breker, M., Strauss-Ayali, D., Viukov, S., Guilliams, M., Misharin, A., et al. (2013) · Immunity · doi:10.1016/j.immuni.2012.12.001 · Cited by 3,245
A Lineage of Myeloid Cells Independent of Myb and Hematopoietic Stem Cells
Schulz, C., Perdiguero, E. G., Chorro, L., Szabo-Rogers, H., Cagnard, N., Kierdorf, K., Prinz, M., Wu, B., Jacobsen, S. E. W., Pollard, J. W., et al. (2012) · Science · doi:10.1126/science.1219179 · Cited by 2,578
Tissue-resident macrophages originate from yolk-sac-derived erythro-myeloid progenitors
Gomez Perdiguero, E., Klapproth, K., Schulz, C., Busch, K., Azzoni, E., Crozet, L., Garner, H., Trouillet, C., de Bruijn, M. F., Geissmann, F., et al. (2015) · Nature · doi:10.1038/nature13989 · Cited by 2,339 · cited 2×
“Furthermore, in examining macrophage development at the early prenatal stages, several Cre transgenic mice under the control of promoters of hematopoietic cell differentiation genes such as runtrelated transcription factor 1 (Runx1) and FMS-like tyrosine kinase 3 (Flt3), were also applied (28,69,70).”
BackgroundMethodDavies, L. C., Jenkins, S. J., Allen, J. E., & Taylor, P. R. (2013) · Nature Immunology · doi:10.1038/ni.2705 · Cited by 2,096
Onset and Progression in Inherited ALS Determined by Motor Neurons and Microglia
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Differential Roles of Macrophages in Diverse Phases of Skin Repair
Lucas, T., Waisman, A., Ranjan, R., Roes, J., Krieg, T., Müller, W., Roers, A., & Eming, S. A. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903356 · Cited by 1,205
Macrophages Facilitate Electrical Conduction in the Heart
Hulsmans, M., Clauss, S., Xiao, L., Aguirre, A. D., King, K. R., Hanley, A., Hucker, W. J., Wülfers, E. M., Seemann, G., Courties, G., et al. (2017) · Cell · doi:10.1016/j.cell.2017.03.050 · Cited by 1,011
Specification of tissue-resident macrophages during organogenesis
Mass, E., Ballesteros, I., Farlik, M., Halbritter, F., Günther, P., Crozet, L., Jacome-Galarza, C. E., Händler, K., Klughammer, J., Kobayashi, Y., et al. (2016) · Science · doi:10.1126/science.aaf4238 · Cited by 891
IL-6 induces an anti-inflammatory response in the absence of SOCS3 in macrophages
Yasukawa, H., Ohishi, M., Mori, H., Murakami, M., Chinen, T., Aki, D., Hanada, T., Takeda, K., Akira, S., Hoshijima, M., et al. (2003) · Nature Immunology · doi:10.1038/ni938 · Cited by 771
USP18 lack in microglia causes destructive interferonopathy of the mouse brain
Goldmann, T., Zeller, N., Raasch, J., Kierdorf, K., Frenzel, K., Ketscher, L., Basters, A., Staszewski, O., Brendecke, S. M., Spiess, A., et al. (2015) · The EMBO Journal · doi:10.15252/embj.201490791 · Cited by 223
Prostaglandin signaling suppresses beneficial microglial function in Alzheimer’s disease models
Johansson, J. U., Woodling, N. S., Wang, Q., Panchal, M., Liang, X., Trueba-Saiz, A., Brown, H. D., Mhatre, S. D., Loui, T., & Andreasson, K. I. (2015) · Journal of Clinical Investigation · doi:10.1172/jci77487 · Cited by 161
Flagged first, then by citations
Research works printed but not linked: 59
- Nagy A (2000) Cre recombinase: the universal reagent for genome tailoring. Genesis 26(2):99–109 · DOI
- Heffner CS, Herbert Pratt C, Babiuk RP et al (2012) Supporting conditional mouse mutagenesis with a comprehensive cre characterization resource. Nat Commun 3:1218. https://doi.org/10.1038/ncomms2186 · DOI
- Kuhn R, Torres RM (2002) Cre/loxP recombination system and gene targeting. Methods Mol Biol 180:175–204. https://doi.org/10.1385/1-59259-178-7:175 · DOI
- Kwan KM (2002) Conditional alleles in mice: practical considerations for tissue-specific knockouts. Genesis 32(2):49–62 · DOI
- Danielian PS, Muccino D, Rowitch DH et al (1998) Modification of gene activity in mouse embryos in utero by a tamoxifen-inducible form of Cre recombinase. Curr Biol 8(24):1323–1326 · DOI
- Srinivas S, Watanabe T, Lin CS et al (2001) Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus. BMC Dev Biol 1:4 · DOI · Paper page
- Buch T, Heppner FL, Tertilt C et al (2005) A Cre-inducible diphtheria toxin receptor mediates cell lineage ablation after toxin administration. Nat Methods 2(6):419–426. https://doi.org/10.1038/nmeth762 · DOI
- Abram CL, Roberge GL, Hu Y et al (2014) Comparative analysis of the efficiency and specificity of myeloid-Cre deleting strains using ROSA-EYFP reporter mice. J Immunol Methods 408:89–100. https://doi.org/10.1016/j.jim.2014.05.009 · DOI
- Short ML, Nickel J, Schmitz A et al (1996) Lysozyme gene expression and regulation. EXS 75:243–257
- Cross M, Renkawitz R (1990) Repetitive sequence involvement in the duplication and divergence of mouse lysozyme genes. EMBO J 9(4):1283–1288 · DOI
- Clausen BE, Burkhardt C, Reith W et al (1999) Conditional gene targeting in macrophages and granulocytes using LysMcre mice. Transgenic Res 8(4):265–277 · DOI · Paper page
- Faust N, Varas F, Kelly LM et al (2000) Insertion of enhanced green fluorescent protein into the lysozyme gene creates mice with green fluorescent granulocytes and macrophages. Blood 96(2):719–726 · DOI
- Ganz T, Gabayan V, Liao HI et al (2003) Increased inflammation in lysozyme M-deficient mice in response to Micrococcus luteus and its peptidoglycan. Blood 101(6):2388–2392. https://doi.org/10.1182/blood-2002-07-2319 · DOI
- Ye M, Iwasaki H, Laiosa CV et al (2003) Hematopoietic stem cells expressing the myeloid lysozyme gene retain long-term, multilineage repopulation potential. Immunity 19(5):689–699 · DOI
- Herbert DR, Holscher C, Mohrs M et al (2004) Alternative macrophage activation is essential for survival during schistosomiasis and downmodulates T helper 1 responses and immunopathology. Immunity 20(5):623–635 · DOI
- Vannella KM, Barron L, Borthwick LA et al (2014) Incomplete deletion of IL-4Ralpha by LysM(Cre) reveals distinct subsets of M2 macrophages controlling inflammation and fibrosis in chronic schistosomiasis. PLoS Pathog 10(9):e1004372. https://doi.org/10.1371/journal.ppat.1004372 · DOI
- Greten FR, Eckmann L, Greten TF et al (2004) IKKbeta links inflammation and tumorigenesis in a mouse model of colitis-associated cancer. Cell 118(3):285–296. https://doi.org/10.1016/j.cell.2004.07.013 · DOI · Paper page
- Kanter JE, Kramer F, Barnhart S et al (2012) Diabetes promotes an inflammatory macrophage phenotype and atherosclerosis through acyl-CoA synthetase 1. Proc Natl Acad Sci U S A 109(12):E715–E724. https://doi.org/10.1073/pnas.1111600109 · DOI
- Goren I, Allmann N, Yogev N et al (2009) A transgenic mouse model of inducible macrophage depletion: effects of diphtheria toxin-driven lysozyme M-specific cell lineage ablation on wound inflammatory, angiogenic, and contractive processes. Am J Pathol 175(1):132–147. https://doi.org/10.2353/ajpath.2009.081002 · DOI
- Meng XM, Wang S, Huang XR et al (2016) Inflammatory macrophages can transdifferentiate into myofibroblasts during renal fibrosis. Cell Death Dis 7(12):e2495. https://doi.org/10.1038/cddis.2016.402 · DOI
- Miyake Y, Kaise H, Isono K et al (2007) Protective role of macrophages in noninflammatory lung injury caused by selective ablation of alveolar epithelial type II Cells. J Immunol 178(8):5001–5009 · DOI
- Sasmono RT, Oceandy D, Pollard JW et al (2003) A macrophage colony-stimulating factor receptor-green fluorescent protein transgene is expressed throughout the mononuclear phagocyte system of the mouse. Blood 101(3):1155–1163. https://doi.org/10.1182/blood-2002-02-0569 · DOI · Paper page
- Deng L, Zhou JF, Sellers RS et al (2010) A novel mouse model of inflammatory bowel disease links mammalian target of rapamycin-dependent hyperproliferation of colonic epithelium to inflammation-associated tumorigenesis. Am J Pathol 176(2):952–967. https://doi.org/10.2353/ajpath.2010.090622 · DOI
- Lin SL, Li B, Rao S et al (2010) Macrophage Wnt7b is critical for kidney repair and regeneration. Proc Natl Acad Sci U S A 107(9):4194–4199. https://doi.org/10.1073/pnas.0912228107 · DOI
- Nissen JC, Tsirka SE (2016) Tuftsin-driven experimental autoimmune encephalomyelitis recovery requires neuropilin-1. Glia 64(6):923–936. https://doi.org/10.1002/glia.22972 · DOI
- Saha S, Aranda E, Hayakawa Y et al (2016) Macrophage-derived extracellular vesicle-packaged WNTs rescue intestinal stem cells and enhance survival after radiation injury. Nat Commun 7:13096. https://doi.org/10.1038/ncomms13096 · DOI
- Stefater JA 3rd, Rao S, Bezold K et al (2013) Macrophage Wnt-Calcineurin-Flt1 signaling regulates mouse wound angiogenesis and repair. Blood 121(13):2574–2578. https://doi.org/10.1182/blood-2012-06-434621 · DOI
- Yeo EJ, Cassetta L, Qian BZ et al (2014) Myeloid WNT7b mediates the angiogenic switch and metastasis in breast cancer. Cancer Res 74(11):2962–2973. https://doi.org/10.1158/0008-5472.CAN-13-2421 · DOI
- Ferron M, Vacher J (2005) Targeted expression of Cre recombinase in macrophages and osteoclasts in transgenic mice. Genesis 41(3):138–145. https://doi.org/10.1002/gene.20108 · DOI
- Evangelidou M, Karamita M, Vamvakas SS et al (2014) Altered expression of oligodendrocyte and neuronal marker genes predicts the clinical onset of autoimmune encephalomyelitis and indicates the effectiveness of multiple sclerosis-directed therapeutics. J Immunol 192(9):4122–4133. https://doi.org/10.4049/jimmunol.1300633 · DOI
- Ferrini F, Trang T, Mattioli TA et al (2013) Morphine hyperalgesia gated through microglia-mediated disruption of neuronal Cl(−) homeostasis. Nat Neurosci 16(2):183–192. https://doi.org/10.1038/nn.3295 · DOI
- Zhang MZ, Yao B, Wang Y et al (2015) Inhibition of cyclooxygenase-2 in hematopoietic cells results in salt-sensitive hypertension. J Clin Invest 125(11):4281–4294. https://doi.org/10.1172/JCI81550 · DOI
- Martens LH, Zhang J, Barmada SJ et al (2012) Progranulin deficiency promotes neuroinflammation and neuron loss following toxin-induced injury. J Clin Invest 122(11):3955–3959. https://doi.org/10.1172/JCI63113 · DOI
- Kwan W, Trager U, Davalos D et al (2012) Mutant huntingtin impairs immune cell migration in Huntington disease. J Clin Invest 122(12):4737–4747. https://doi.org/10.1172/JCI64484 · DOI
- Robblee MM, Kim CC, Porter Abate J et al (2016) Saturated fatty acids engage an IRE1alpha-dependent pathway to activate the NLRP3 inflammasome in myeloid cells. Cell Rep 14(11):2611–2623. https://doi.org/10.1016/j.celrep.2016.02.053 · DOI
- Sugatani T, Hruska KA (2009) Impaired micro-RNA pathways diminish osteoclast differentiation and function. J Biol Chem 284(7):4667–4678. https://doi.org/10.1074/jbc.M805777200 · DOI · Paper page
- Yu M, Zhou H, Zhao J et al (2014) MyD88-dependent interplay between myeloid and endothelial cells in the initiation and progression of obesity-associated inflammatory diseases. J Exp Med 211(5):887–907. https://doi.org/10.1084/jem.20131314 · DOI
- Schaller E, Macfarlane AJ, Rupec RA et al (2002) Inactivation of the F4/80 glycoprotein in the mouse germ line. Mol Cell Biol 22(22):8035–8043 · DOI
- Weichand B, Weis N, Weigert A et al (2013) Apoptotic cells enhance sphingosine-1-phosphate receptor 1 dependent macrophage migration. Eur J Immunol 43(12):3306–3313. https://doi.org/10.1002/eji.201343441 · DOI
- Zhang Z, Zhang F, An P et al (2011) Ferroportin1 deficiency in mouse macrophages impairs iron homeostasis and inflammatory responses. Blood 118(7):1912–1922. https://doi.org/10.1182/blood-2011-01-330324 · DOI · Paper page
- Tan SY, Krasnow MA (2016) Developmental origin of lung macrophage diversity. Development 143(8):1318–1327. https://doi.org/10.1242/dev.129122 · DOI
- Parkhurst CN, Yang G, Ninan I et al (2013) Microglia promote learning-dependent synapse formation through brain-derived neurotrophic factor. Cell 155(7):1596–1609. https://doi.org/10.1016/j.cell.2013.11.030 · DOI · Paper page
- Aychek T, Mildner A, Yona S et al (2015) IL-23-mediated mononuclear phagocyte crosstalk protects mice from Citrobacter rodentium-induced colon immunopathology. Nat Commun 6:6525. https://doi.org/10.1038/ncomms7525 · DOI
- Cain DW, O’Koren EG, Kan MJ et al (2013) Identification of a tissue-specific, C/EBPbeta-dependent pathway of differentiation for murine peritoneal macrophages. J Immunol 191(9):4665–4675. https://doi.org/10.4049/jimmunol.1300581 · DOI
- Kim KW, Williams JW, Wang YT et al (2016) MHC II+ resident peritoneal and pleural macrophages rely on IRF4 for development from circulating monocytes. J Exp Med 213(10):1951–1959. https://doi.org/10.1084/jem.20160486 · DOI
- Molawi K, Wolf Y, Kandalla PK et al (2014) Progressive replacement of embryo-derived cardiac macrophages with age. J Exp Med 211(11):2151–2158. https://doi.org/10.1084/jem.20140639 · DOI
- Theurl I, Hilgendorf I, Nairz M et al (2016) On-demand erythrocyte disposal and iron recycling requires transient macrophages in the liver. Nat Med 22(8):945–951. https://doi.org/10.1038/nm.4146 · DOI · Paper page
- DeFalco T, Bhattacharya I, Williams AV et al (2014) Yolk-sac-derived macrophages regulate fetal testis vascularization and morphogenesis. Proc Natl Acad Sci U S A 111(23):E2384–E2393. https://doi.org/10.1073/pnas.1400057111 · DOI
- Batti L, Sundukova M, Murana E et al (2016) TMEM16F regulates spinal microglial function in neuropathic pain states. Cell Rep 15(12):2608–2615. https://doi.org/10.1016/j.celrep.2016.05.039 · DOI
- Goldmann T, Wieghofer P, Muller PF et al (2013) A new type of microglia gene targeting shows TAK1 to be pivotal in CNS autoimmune inflammation. Nat Neurosci 16(11):1618–1626. https://doi.org/10.1038/nn.3531 · DOI · Paper page
- Lewitus GM, Konefal SC, Greenhalgh AD et al (2016) Microglial TNF-alpha suppresses cocaine-induced plasticity and behavioral sensitization. Neuron 90(3):483–491. https://doi.org/10.1016/j.neuron.2016.03.030 · DOI
- Li D, Wang C, Yao Y et al (2016) mTORC1 pathway disruption ameliorates brain inflammation following stroke via a shift in microglia phenotype from M1 type to M2 type. FASEB J 30(10):3388–3399. https://doi.org/10.1096/fj.201600495R · DOI
- Wolf Y, Shemer A, Polonsky M et al (2017) Autonomous TNF is critical for in vivo monocyte survival in steady state and inflammation. J Exp Med 214(4):905–917. https://doi.org/10.1084/jem.20160499 · DOI
- Gao H, Danzi MC, Choi CS et al (2017) Opposing functions of microglial and macrophagic TNFR2 in the pathogenesis of experimental autoimmune encephalomyelitis. Cell Rep 18(1):198–212. https://doi.org/10.1016/j.celrep.2016.11.083 · DOI
- Peng J, Gu N, Zhou L et al (2016) Microglia and monocytes synergistically promote the transition from acute to chronic pain after nerve injury. Nat Commun 7:12029. https://doi.org/10.1038/ncomms12029 · DOI · Paper page
- Kaplan DH, Li MO, Jenison MC et al (2007) Autocrine/paracrine TGFbeta1 is required for the development of epidermal Langerhans cells. J Exp Med 204(11):2545–2552. https://doi.org/10.1084/jem.20071401 · DOI · Paper page
- Zahner SP, Kel JM, Martina CA et al (2011) Conditional deletion of TGF-betaR1 using Langerin-Cre mice results in Langerhans cell deficiency and reduced contact hypersensitivity. J Immunol 187(10):5069–5076. https://doi.org/10.4049/jimmunol.1101880 · DOI
- Samokhvalov IM, Samokhvalova NI, Nishikawa S (2007) Cell tracing shows the contribution of the yolk sac to adult haematopoiesis. Nature 446(7139):1056–1061. https://doi.org/10.1038/nature05725 · DOI
- Boiers C, Carrelha J, Lutteropp M et al (2013) Lymphomyeloid contribution of an immune-restricted progenitor emerging prior to definitive hematopoietic stem cells. Cell Stem Cell 13(5):535–548. https://doi.org/10.1016/j.stem.2013.08.012 · DOI
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“9 12 Compared with other recently generated lines such as Sall1 CreER13 or Cd11b Cre , 14 there is less recombination in other brain or immune cell types.”
Macrophage INSIG1 deficiency drives psoriasiform dermatitis via the SREBP2-STAT1 axis
Li, X., Zang, Y., Li, X., Sheng, T., Liu, S., Chen, L., Xu, X., Wang, L., Long, R., Zhang, M., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-73278-8 · Cited by 1
Metadata
- Authors
- Shi, J., Hua, L., Harmer, D., Li, P., & Ren, G.
- Venue
- Methods in Molecular Biology
- Publisher
- Springer New York
- Published
- 2018
- Pages
- 263-275
- ISSN
- 1064-3745
- 1940-6029
- PMC
- PMC6331202
- Cited by
- 145
- References
- 11
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