Reelin Deficiency Delays Mammary Tumor Growth and Metastatic Progression
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Abstract
Reelin is a regulator of cell migration in the nervous system, and has other functions in the development of a number of non-neuronal tissues. In addition, alterations in reelin expression levels have been reported in breast, pancreatic, liver, gastric, and other cancers. Reelin is normally expressed in mammary gland stromal cells, but whether stromal reelin contributes to breast cancer progression is unknown. Herein, we used a syngeneic mouse mammary tumor transplantation model to examine the impact of host-derived reelin on breast cancer progression. We found that transplanted syngeneic tumors grew more slowly in reelin-deficient (rl Orl −/− ) mice and had delayed metastatic colonization of the lungs. Immunohistochemistry of primary tumors revealed that tumors grown in rl Orl −/− animals had fewer blood vessels and increased macrophage infiltration. Gene expression studies from tumor tissues indicate that loss of host-derived reelin alters the balance of M1- and M2-associated macrophage markers, suggesting that reelin may influence the polarization of these cells. Consistent with this, rl Orl −/− M1-polarized bone marrow-derived macrophages have heightened levels of the M1-associated cytokines iNOS and IL-6. Based on these observations, we propose a novel function for the reelin protein in breast cancer progression.
Keywords
Reelin Breast cancer 4T1 Tumor-associated macrophageNotes
Acknowledgements
We thank Dr. Patricia Phelps, Dr. Cristina Ghiani, Dr. Catalina Abad Rabat and Dr. Diana Moughon for kindly providing reagents and for thoughtful discussion. We are thankful to Donna Crandall for assistance with figure preparation and Joseph Argus for assistance with manuscript editing.
Compliance with Ethical Standards
Grants
These studies were supported by the National Institute of Child Health and Development R03 HD075840 - https://www.nichd.nih.gov/Pages/index.aspx and the California Breast Cancer Research Program 161B-0110 - http://www.cbcrp.org/to EMC. EK was supported by the Whitcome Fellowship of the UCLA Molecular Biology Institute. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Conflict of Interest
The authors declare that they have no conflict of interest.
Ethics Approval
All animal studies were conducted in accordance with the UCLA Office of Animal Research Oversight and Institutional Animal Care and Use Committee protocols.
Supplementary material
Metastasis of 4T1 cells in rl Orl −/− and rl Orl +/+ mice bearing similar-sized tumors. (a) Wet weight of primary tumors collected 25 days (rl Orl +/+ , n = 8) and 29 days (rl Orl −/− , n = 9) after 4T1 cell injection. (b) Quantification of metastatic burden in the lungs. ns – not significant. Statistical significance determined using two-tailed, unpaired Student’s t-test. (GIF 8 kb)
Cytokine expression levels in rl Orl −/− and rl Orl +/+ BMDM treated with 4T1-conditioned medium for 24 h. Gene expression levels are relative to those in rl Orl +/+ BMDM controls. *P < 0.05, ns – not significant. Statistical significance determined using two-tailed, unpaired Student’s t-test. (GIF 6 kb)
Cytokine expression levels in rl Orl +/+ BMDM treated with IFNγ and LPS. Gene expression levels are relative to those in unstimulated rl Orl +/+ BMDM controls. (GIF 10 kb)
References
- 1.Fatemi SH. Reelin glycoprotein: structure, biology, and roles in health and disease. New York: Springer; 2008.CrossRefGoogle Scholar
- 2.Honda T, Kobayashi K, Mikoshiba K, Nakajima K. Regulation of cortical neuron migration by the reelin signaling pathway. Neurochem Res. 2011;36(7):1270–9.CrossRefPubMedGoogle Scholar
- 3.Abadesco AD, Cilluffo M, Yvone GM, Carpenter EM, Howell BW, Phelps PE. Novel disabled-1-expressing neurons identified in adult brain and spinal cord. Eur J Neurosci. 2014;39:579–92.CrossRefPubMedGoogle Scholar
- 4.D’Arcangelo G. Reelin in the years: controlling neuronal migration and maturation in the mammalian brain. Adv Neurosci. doi: 10.1155/2014/597395.
- 5.Herz J, Chen Y. Reelin, lipoprotein receptors and synaptic plasticity. Nat Rev Neurosci. 2006;7(11):850–9.CrossRefPubMedGoogle Scholar
- 6.Bock HH, Herz J. Reelin activates SRC family tyrosine kinases in neurons. Curr Biol. 2003;13(1):18–26.CrossRefPubMedGoogle Scholar
- 7.Kuo G, Arnaud L, Kronstad-O’Brien P, Cooper JA. Absence of Fyn and Src causes a reeler-like phenotype. J Neurosci. 2005;25(37):8578–86.CrossRefPubMedGoogle Scholar
- 8.Diaz-Mendoza MJ, Lorda-Diez CI, Montero JA, Garcia-Porrero JA, Hurle JM. Reelin/DAB-1 signaling in the embryonic limb regulates the chondrogenic differentiation of digit mesodermal progenitors. J Cell Physiol. 2014;229(10):1397–404.CrossRefPubMedGoogle Scholar
- 9.Botella-López A, de Madaria E, Jover R, Bataller R, Sancho-Bru P, Candela A, et al. Reelin is overexpressed in the liver and plasma of bile duct ligated rats and its levels and glycosylation are altered in plasma of humans with cirrhosis. Int J Biochem Cell Biol. 2008;40(4):766–75.CrossRefPubMedGoogle Scholar
- 10.Tseng WL, Chen TH, Huang CC, Huang YH, Yeh CF, Tsai HJ, et al. Impaired thrombin generation in reelin-deficient mice: a potential role of plasma reelin in hemostasis. J Thromb Haemost. 2014;12(12):1–11.CrossRefGoogle Scholar
- 11.Vázquez-Carretero MD, García-Miranda P, Calonge ML, Peral MJ, Ilundain AA. Dab1 and reelin participate in a common signal pathway that controls intestinal crypt/villus unit dynamics. Biol Cell. 2014;106(3):83–96.CrossRefPubMedGoogle Scholar
- 12.Lutter S, Xie S, Tatin F, Makinen T. Smooth muscle-endothelial cell communication activates reelin signaling and regulates lymphatic vessel formation. J Cell Biol. 2012;197(6):837–49.CrossRefPubMedPubMedCentralGoogle Scholar
- 13.Khialeeva E, Lane TF, Carpenter EM. Disruption of reelin signaling alters mammary gland morphogenesis. Development. 2011;138(4):767–76.CrossRefPubMedPubMedCentralGoogle Scholar
- 14.Hong SM, Kelly D, Griffith M, Omura N, Li A, Li CP, et al. Multiple genes are hypermethylated in intraductal papillary mucinous neoplasms of the pancreas. Mod Pathol. 2008;21(12):1499–507.CrossRefPubMedPubMedCentralGoogle Scholar
- 15.Dohi O, Takada H, Wakabayashi N, Yasui K, Sakakura C, Mitsufuji S, et al. Epigenetic silencing of RELN in gastric cancer. Int J Oncol. 2010;36(1):85–92.PubMedGoogle Scholar
- 16.Perrone G, Vincenzi B, Zagami M, Santini D, Panteri R, Flammia G, et al. Reelin expression in human prostate cancer: a marker of tumor aggressiveness based on correlation with grade. Mod Pathol. 2007;20(3):344–51.CrossRefPubMedGoogle Scholar
- 17.Wang Q, Lu J, Yang C, Wang X, Cheng L, Hu G, et al. CASK and its target gene reelin were co-upregulated in human esophageal carcinoma. Cancer Lett. 2002;179(1):71–7.CrossRefPubMedGoogle Scholar
- 18.Stein T, Cosimo E, Yu X, Smith PR, Simon R, Cottrell L, et al. Loss of reelin expression in breast cancer is epigenetically controlled and associated with poor prognosis. Am J Pathol. 2010;177(5):2323–33.CrossRefPubMedPubMedCentralGoogle Scholar
- 19.Pulaski BA, Ostrand-Rosenberg S. Mouse 4 T1 breast tumor model. Curr Protoc Immunol. 2001; Chapter 20:Unit 20.2.Google Scholar
- 20.Takahara T, Ohsumi T, Kuromitsu J, Shibata K, Sasaki N, Okazaki Y, et al. Dysfunction of the Orleans reeler gene arising from exon skipping due to transposition of a full-length copy of an active L1 sequence into the skipped exon. Hum Mol Genet. 1996;5(7):989–93.CrossRefPubMedGoogle Scholar
- 21.De Bergeyck V, Nakajima K, Lambert de Rouvrait C, Naerhuyzen B, Goffinet AM, Miyata T, et al. A truncated reelin protein is produced but not secreted in the “Orleans” reeler mutation (Reln(rl-Orl)). Brain Res Mol Brain Res. 1997;50(1–2):85–90.CrossRefPubMedGoogle Scholar
- 22.D’Arcangelo G, Homayouni R, Keshvara L, Rice DS, Sheldon M, Curran T. Reelin is a ligand for lipoprotein receptors. Neuron. 1999;24(2):471–9.CrossRefPubMedGoogle Scholar
- 23.Ewald AJ. Isolation of mouse mammary organoids for long-term time-lapse imaging. Cold Spring Harb Protoc. 2013;2013(2):130–3.PubMedGoogle Scholar
- 24.Kim EJ, Choi MR, Park H, Kim M, Hong JE, Lee JY, et al. Dietary fat increases solid tumor growth and metastasis of 4 T1 murine mammary carcinoma cells and mortality in obesity-resistant BALB/c mice. Breast Cancer Res. 2011;13(4):R78.CrossRefPubMedPubMedCentralGoogle Scholar
- 25.York AG, Williams KJ, Argus JP, Zhou QD, Brar G, Vergnes L, et al. Limiting cholesterol biosynthetic flux spontaneously engages type I IFN signaling. Cell. 2015;163(7):1716–29.CrossRefPubMedPubMedCentralGoogle Scholar
- 26.Falconer D. Two new mutants, ‘trembler'and 'reeler', with neurological actions in the house mouse (Mus musculus L.). J Genet. 1951;50(2):192–205.CrossRefPubMedGoogle Scholar
- 27.DuPré SA, Redelman D, Hunter KW. The mouse mammary carcinoma 4 T1: characterization of the cellular landscape of primary tumours and metastatic tumour foci. Int J Exp Pathol. 2007;88(5):351–60.CrossRefPubMedPubMedCentralGoogle Scholar
- 28.Cho HJ, Jung JI, Lim DY, Kwon GT, Her S, Park JH, et al. Bone marrow-derived, alternatively-activated macrophages enhance solid tumor growth and lung metastasis of mammary carcinoma cells in a Balb/C mouse orthotopic model. Breast Cancer Res. 2012;14(3):R81.CrossRefPubMedPubMedCentralGoogle Scholar
- 29.Green-Johnson JM, Zalcman S, Vriend CY, Nance DM, Greenberg AH. Suppressed T cell and macrophage function in the“ reeler”(rl/rl) mutant, a murine strain with elevated cerebellar norepinephrine concentration. Brain Behav Immun. 1995;9(1):47–60.CrossRefPubMedGoogle Scholar
- 30.Murdoch C, Muthana M, Coffelt SB, Lewis CE. The role of myeloid cells in the promotion of tumour angiogenesis. Nat Rev Cancer. 2008;8(8):618–31.CrossRefPubMedGoogle Scholar
- 31.Mills CD. M1 and M2 macrophages: oracles of health and disease. Crit Rev Immunol. 2012;32(6):463–88.CrossRefPubMedGoogle Scholar
- 32.Ma J, Liu L, Che G, Yu N, Dai F, You Z. The M1 form of tumor-associated macrophages in non-small cell lung cancer is positively associated with survival time. BMC Cancer. 2010;10:112.CrossRefPubMedPubMedCentralGoogle Scholar
- 33.Mantovani A, Sozzani S, Locati M, Allavena P, Sica A. Macrophage polarization: tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes. Trends Immunol. 2002;23(11):549–55.CrossRefPubMedGoogle Scholar
- 34.Saraiva M, O’Garra A. The regulation of IL-10 production by immune cells. Nat Rev Immunol. 2010;10(3):170–81.CrossRefPubMedGoogle Scholar
- 35.Trinchieri G. Interleukin-10 production by effector T cells: Th1 cells show self control. J Exp Med. 2007;204(2):239–43.CrossRefPubMedPubMedCentralGoogle Scholar
- 36.Pineda-Torra I, Gage M, de Juan A, Pello OM. Isolation, culture and polarization of murine bone marrow-derived and peritoneal macrophages. Methods Mol Biol. 2015;1339:101–9.CrossRefPubMedGoogle Scholar
- 37.Schroder K, Hertzog PJ, Ravasi T, Hume DA. Interferon-gamma: an overview of signals, mechanisms and functions. J Leukoc Biol. 2004;75(2):163–89.CrossRefPubMedGoogle Scholar
- 38.Boonstra A, Rajsbaum R, Holman M, Marques R, Asselin-Paturel C, Pereira JP, et al. Macrophages and myeloid dendritic cells, but not plasmacytoid dendritic cells, produce IL-10 in response to MyD88- and TRIF-dependent TLR signals, and TLR-independent signals. J Immunol. 2006;177(11):7551–8.CrossRefPubMedGoogle Scholar
- 39.Martinez FO, Gordon S. The M1 and M2 paradigm of macrophage activation: time for reassessment. F1000Prime Rep. 2014;3:1–13.Google Scholar
- 40.Pulaski BA, Ostrand-Rosenberg S. Reduction of established spontaneous mammary carcinoma metastases following immunotherapy with major histocompatibility complex class II and B7.1 cell-based tumor vaccines. Cancer Res. 1998;58(7):1486–93.PubMedGoogle Scholar
- 41.Thomas DL, Fraser NW. HSV-1 therapy of primary tumors reduces the number of metastases in an immune-competent model of metastatic breast cancer. Mol Ther. 2003;8(4):543–51.CrossRefPubMedGoogle Scholar
- 42.Aslakson CJ, Miller FR. Selective events in the metastatic process defined by analysis of the sequential dissemination of subpopulations of a mouse mammary tumor. Cancer Res. 1992;52(6):1399–405.PubMedGoogle Scholar
- 43.Kessenbrock K, Plaks V, Werb Z. Matrix metalloproteinases: regulators of the tumor microenvironment. Cell. 2010;141(1):52–67.CrossRefPubMedPubMedCentralGoogle Scholar
- 44.Stubbs D, DeProto J, Nie K, Englund C, Mahmud I, Hevner R, et al. Neurovascular congruence during cerebral cortical development. Cereb Cortex. 2009;19(suppl 1):i32–41.CrossRefPubMedPubMedCentralGoogle Scholar
- 45.Guy J, Wagener RJ, Möck M, Staiger JF. Persistence of functional sensory maps in the absence of cortical layers in the somsatosensory cortex of reeler mice. Cereb Cortex. 2015;25(9):2517–28.CrossRefPubMedGoogle Scholar
- 46.Kopmels B, Wollman EE, Guastavino JM, Delhaye-Bouchaud N, Fradelizi D, Mariani J. Interleukin-1 hyperproduction by in vitro activated peripheral macrophages from cerebellar mutant mice. J Neurochem. 1990;55(6):1980–5.CrossRefPubMedGoogle Scholar
- 47.Bakalian A, Kopmels B, Messer A, Fradelizi D, Delhaye-Bouchaud N, Wollman E, et al. Peripheral macrophage abnormalities in mutant mice with spinocerebellar degeneration. Res Immunol. 1992;143(1):129–39.CrossRefPubMedGoogle Scholar
- 48.Rivera-Baltanas T, Romay-Tallon R, Dopeso-Reyes IG, Caruncho HJ. Serotonin transporter clustering in blood lymphocytes of reeler mice. Cardiovasc Psychiatry Neurol. 2010;2010:396282.CrossRefPubMedPubMedCentralGoogle Scholar
- 49.Resende C, Ristimäki A, Machado JC. Genetic and epigenetic alteration in gastric carcinogenesis. Helicobacter. 2010;15(suppl I):34–9.CrossRefPubMedGoogle Scholar
- 50.Berthier-Vergnes O, El KM, de la Fouchardière A, Pointecouteau T, Verrando P, Wierinckx A, et al. Gene expression profiles of human melanoma cells with different invasive potential reveal TSPAN8 as a novel mediator of invasion. Br J Cancer. 2011;104(1):155–65.CrossRefPubMedGoogle Scholar
- 51.Zhang J, Ding L, Holmfeldt L, Wu G, Heatley SL, Payne-Turner D, et al. The genetic basis of early T-cell precursor acute lymphoblastic leukaemia. Nature. 2012;481(7380):157–63.CrossRefPubMedPubMedCentralGoogle Scholar