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1 1 Gao, X., Xu, C., Asada, N., and Frenette, P.S. (2018). The hematopoietic stem cell niche: from embryo to adult. Development 145 (2): dev139691.

2 2 Fitch, S.R., Kimber, G.M., Wilson, N.K. et al. (2012). Signaling from the sympathetic nervous system regulates hematopoietic stem cell emergence during embryogenesis. Cell Stem Cell 11 (4): 554–566.

3 3 Mariani, S.A., Li, Z., Rice, S. et al. (2019). Pro‐inflammatory aorta‐associated macrophages are involved in embryonic development of hematopoietic stem cells. Immunity 50 (6): 1439–1452. e5.

4 4 Willard‐Mack, C.L., Elmore, S.A., Hall, W.C. et al. (2019). Nonproliferative and proliferative lesions of the rat and mouse hematolymphoid system. Toxicol. Pathol. 47 (6): 665–783.

5 5 Pinho, S. and Frenette, P.S. (2019). Haematopoietic stem cell activity and interactions with the niche. Nat. Rev. Mol. Cell Biol. 20 (5): 303–320.

6 6 Pioli, P.D., Casero, D., Montecino‐Rodriguez, E. et al. (2019). Plasma cells are obligate effectors of enhanced myelopoiesis in aging bone marrow. Immunity 51 (2): 351–366. e6.

7 7 Sass, B. and Montali, R.J. (1980). Spontaneous fibro‐osseous lesions in aging female mice. Lab. Anim. Sci. 30 (5): 907–909.

8 8 Albassam, M.A., Wojcinski, Z.W., Barsoum, N.J., and Smith, G.S. (1991). Spontaneous fibro‐osseous proliferative lesions in the sternums and femurs of B6C3F1 mice. Vet. Pathol. 28 (5): 381–388.

9 9 Berndt, A., Ackert‐Bicknell, C., Silva, K.A. et al. (2016). Genetic determinants of fibro‐osseous lesions in aged inbred mice. Exp. Mol. Pathol. 100 (1): 92–100.

10 10 Rodewald, H.R. (2008). Thymus organogenesis. Annu. Rev. Immunol. 26: 355–388.

11 11 de Vries, M.J. and Hijmans, W. (1967). Pathological changes of thymic epithelial cells and autoimmune disease in NZB, NZW and (NZB x NZW)F1 mice. Immunology 12 (2): 179–196.

12 12 Li, L., Hsu, H.C., Grizzle, W.E. et al. (2003). Cellular mechanism of thymic involution. Scand. J. Immunol. 57 (5): 410–422.

13 13 Xu, P.X., Adams, J., Peters, H. et al. (1999). Eya1‐deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia. Nat. Genet. 23 (1): 113–117.

14 14 Xu, P.X., Zheng, W., Laclef, C. et al. (2002). Eya1 is required for the morphogenesis of mammalian thymus, parathyroid and thyroid. Development 129 (13): 3033–3044.

15 15 Nehls, M., Kyewski, B., Messerle, M. et al. (1996). Two genetically separable steps in the differentiation of thymic epithelium. Science 272 (5263): 886–889.

16 16 Manley, N.R. and Capecchi, M.R. (1998). Hox group 3 paralogs regulate the development and migration of the thymus, thyroid, and parathyroid glands. Dev. Biol. 195 (1): 1–15.

17 17 Dietrich, S. and Gruss, P. (1995). undulated phenotypes suggest a role of Pax‐1 for the development of vertebral and extravertebral structures. Dev. Biol. 167 (2): 529–548.

18 18 Conway, S.J., Henderson, D.J., and Copp, A.J. (1997). Pax3 is required for cardiac neural crest migration in the mouse: evidence from the splotch (Sp2H) mutant. Development 124 (2): 505–514.

19 19 Peters, H., Neubuser, A., Kratochwil, K., and Balling, R. (1998). Pax9‐deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities. Genes Dev. 12 (17): 2735–2747.

20 20 Laclef, C., Souil, E., Demignon, J., and Maire, P. (2003). Thymus, kidney and craniofacial abnormalities in Six 1 deficient mice. Mech. Dev. 120 (6): 669–679.

21 21 Jerome, L.A. and Papaioannou, V.E. (2001). DiGeorge syndrome phenotype in mice mutant for the T‐box gene, Tbx1. Nat. Genet. 27 (3): 286–291.

22 22 Custer, R.P., Bosma, G.C., and Bosma, M.J. (1985). Severe combined immunodeficiency (SCID) in the mouse. Pathology, reconstitution, neoplasms. Am. J. Pathol. 120 (3): 464–477.

23 23 Mombaerts, P., Iacomini, J., Johnson, R.S. et al. (1992). RAG‐1‐deficient mice have no mature B and T lymphocytes. Cell 68 (5): 869–877.

24 24 Shinkai, Y., Rathbun, G., Lam, K.P. et al. (1992). RAG‐2‐deficient mice lack mature lymphocytes owing to inability to initiate V(D). J. Rearrangement. Cell 68 (5): 855–867.

25 25 DiSanto, J.P., Muller, W., Guy‐Grand, D. et al. (1995). Lymphoid development in mice with a targeted deletion of the interleukin 2 receptor gamma chain. Proc. Natl. Acad. Sci. U.S.A. 92 (2): 377–381.

26 26 Cao, X., Shores, E.W., Hu‐Li, J. et al. (1995). Defective lymphoid development in mice lacking expression of the common cytokine receptor gamma chain. Immunity 2 (3): 223–238.

27 27 Pearse, G. (2006). Histopathology of the thymus. Toxicol. Pathol. 34 (5): 515–547.

28 28 Burnet, F.M. and Holmes, M.C. (1964). Thymic changes in the mouse strain Nzb in relation to the auto‐immune state. J. Pathol. Bacteriol. 88: 229–241.

29 29 Van den Broeck, W., Derore, A., and Simoens, P. (2006). Anatomy and nomenclature of murine lymph nodes: descriptive study and nomenclatory standardization in BALB/cAnNCrl mice. J. Immunol. Methods 312 (1–2): 12–19.

30 30 van de Pavert, S.A. and Mebius, R.E. (2010). New insights into the development of lymphoid tissues. Nat. Rev. Immunol. 10 (9): 664–674.

31 31 Onder, L. and Ludewig, B. (2018). A fresh view on lymph node organogenesis. Trends Immunol. 39 (10): 775–787.

32 32 Colbeck, E.J., Ager, A., Gallimore, A., and Jones, G.W. (2017). Tertiary lymphoid structures in cancer: drivers of antitumor immunity, immunosuppression, or bystander sentinels in disease? Front. Immunol. 8: 1830.

33 33 Buckley, C.D., Barone, F., Nayar, S. et al. (2015). Stromal cells in chronic inflammation and tertiary lymphoid organ formation. Annu. Rev. Immunol. 33: 715–745.

34 34 Bellomo, A., Gentek, R., Bajenoff, M., and Baratin, M. (2018). Lymph node macrophages: scavengers, immune sentinels and trophic effectors. Cell. Immunol. 330: 168–174.

35 35 Pasparakis, M., Alexopoulou, L., Episkopou, V., and Kollias, G. (1996). Immune and inflammatory responses in TNF alpha‐deficient mice: a critical requirement for TNF alpha in the formation of primary B cell follicles, follicular dendritic cell networks and germinal centers, and in the maturation of the humoral immune response. J. Exp. Med. 184 (4): 1397–1411.

36 36 De Togni, P., Goellner, J., Ruddle, N.H. et al. (1994). Abnormal development of peripheral lymphoid organs in mice deficient in lymphotoxin. Science 264 (5159): 703–707.

37 37 Banks, T.A., Rouse, B.T., Kerley, M.K. et al. (1995). Lymphotoxin‐alpha‐deficient mice. Effects on secondary lymphoid organ development and humoral immune responsiveness. J. Immunol. 155 (4): 1685–1693.

38 38 Koni, P.A., Sacca, R., Lawton, P. et al. (1997). Distinct roles in lymphoid organogenesis for lymphotoxins alpha and beta revealed in lymphotoxin beta‐deficient mice. Immunity 6 (4): 491–500.

39 39 Alimzhanov, M.B., Kuprash, D.V., Kosco‐Vilbois, M.H. et al. (1997). Abnormal development of secondary lymphoid tissues in lymphotoxin beta‐deficient mice. Proc. Natl. Acad. Sci. U.S.A. 94 (17): 9302–9307.

40 40 Futterer, A., Mink, K., Luz, A. et al. (1998). The lymphotoxin beta receptor controls organogenesis and affinity maturation in peripheral lymphoid tissues. Immunity 9 (1): 59–70.

41 41 Kong, Y.Y., Yoshida, H., Sarosi, I. et al. (1999). OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph‐node organogenesis. Nature 397 (6717): 315–323.

42 42 Dougall, W.C., Glaccum, M., Charrier, K. et al. (1999). RANK is essential for osteoclast and lymph node development. Genes Dev. 13 (18): 2412–2424.

43 43 Weih, F. and Caamano, J. (2003). Regulation of secondary lymphoid organ development by the nuclear factor‐kappaB signal transduction pathway. Immunol. Rev. 195: 91–105.

44 44 Miyawaki, S., Nakamura, Y., Suzuka, H. et al. (1994). A new mutation, aly, that induces a generalized lack of lymph nodes accompanied by immunodeficiency in mice. Eur. J. Immunol. 24 (2): 429–434.

45 45 Fukuyama, S., Hiroi, T., Yokota, Y. et al. (2002). Initiation of NALT organogenesis is independent of the IL‐7R, LTbetaR, and NIK signaling pathways but requires the Id2 gene and CD3(−)CD4(+)CD45(+) cells. Immunity 17 (1): 31–40.

46 46 Yokota, Y., Mansouri, A., Mori, S. et al. (1999). Development of peripheral lymphoid organs and natural killer cells depends on the helix‐loop‐helix inhibitor Id2. Nature 397 (6721): 702–706.

47 47 Sun, Z., Unutmaz, D., Zou, Y.R. et al. (2000). Requirement for RORgamma in thymocyte survival and lymphoid organ development. Science 288 (5475): 2369–2373.

48 48 Tachibana, M., Tenno, M., Tezuka, C. et al. (2011). Runx1/Cbfbeta2 complexes are required for lymphoid tissue inducer cell differentiation at two developmental stages. J. Immunol. 186 (3): 1450–1457.

49 49 Nagatake, T., Fukuyama, S., Sato, S. et al. (2015). Central role of core binding factor beta2 in mucosa‐associated lymphoid tissue organogenesis in mouse. PLoS One 10 (5): e0127460.

50 50 Ansel, K.M., Ngo, V.N., Hyman, P.L. et al. (2000). A chemokine‐driven positive feedback loop organizes lymphoid follicles. Nature 406 (6793): 309–314.

51 51 Turner, V.M. and Mabbott, N.A. (2017). Structural and functional changes to lymph nodes in ageing mice. Immunology 151 (2): 239–247.

52 52 Terahara, K., Yoshida, M., Igarashi, O. et al. (2008). Comprehensive gene expression profiling of Peyer's patch M cells, villous M‐like cells, and intestinal epithelial cells. J. Immunol. 180 (12): 7840–7846.

53 53 Adachi, S., Yoshida, H., Kataoka, H., and Nishikawa, S. (1997). Three distinctive steps in Peyer's patch formation of murine embryo. Int. Immunol. 9 (4): 507–514.

54 54 Seymour, R., Shirley, B.J., HogenEsch, H. et al. (2013). Loss of function of the mouse sharpin gene results in Peyer's patch regression. PLoS One 8 (2): e55224.

55 55 Aw, D., Hilliard, L., Nishikawa, Y. et al. (2016). Disorganization of the splenic microanatomy in ageing mice. Immunology 148 (1): 92–101.

56 56 Turner, V.M. and Mabbott, N.A. (2017). Influence of ageing on the microarchitecture of the spleen and lymph nodes. Biogerontology 18 (5): 723–738.

57 57 Lundmark, K., Vahdat Shariatpanahi, A., and Westermark, G.T. (2013). Depletion of spleen macrophages delays AA amyloid development: a study performed in the rapid mouse model of AA amyloidosis. PLoS One 8 (11): e79104.

58 58 Rangel‐Moreno, J., Moyron‐Quiroz, J.E., Carragher, D.M. et al. (2009). Omental milky spots develop in the absence of lymphoid tissue‐inducer cells and support B and T cell responses to peritoneal antigens. Immunity 30 (5): 731–743.

59 59 Meza‐Perez, S. and Randall, T.D. (2017). Immunological functions of the omentum. Trends Immunol. 38 (7): 526–536.

60 60 Hu, D., Mohanta, S.K., Yin, C. et al. (2015). Artery tertiary lymphoid organs control aorta immunity and protect against atherosclerosis via vascular smooth muscle cell lymphotoxin beta receptors. Immunity 42 (6): 1100–1115.

61 61 Sautes‐Fridman, C., Petitprez, F., Calderaro, J., and Fridman, W.H. (2019). Tertiary lymphoid structures in the era of cancer immunotherapy. Nat. Rev. Cancer 19 (6): 307–325.

Pathology of Genetically Engineered and Other Mutant Mice

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