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. Author manuscript; available in PMC: 2016 Jan 1.
Published in final edited form as: J Immunol. 2014 Nov 24;194(1):334–348. doi: 10.4049/jimmunol.1401548

Table I.

Summary of histological observations of M-TRAF3−/− mice at the age of 15–22 months

Mice examined (n=22) Number Organs involved
Tumor
 Histiocytic sarcoma 2 Spleen, liver
 Hepatocellular adenoma 1 Liver
 B cell lymphoma (DLBCL or FL) 9 Spleen, CLN, MLN, liver
Inflammation 6 Liver, GI tract, lung, kidney, pancreas, heart
Infection 3 GI tract, liver, lung
Unknown
 hemorrhage 7
 blister 2
Normal 7

Histologic diagnoses were made based on established criteria (2328). Mice with DLBCL and FL were diagnosed histologically using criteria outlined in a consensus nomenclature of mouse lymphoid neoplasms (23). Malignancies of histiocytes (histiocytic sarcoma) were diagnosed histologically as described (24). Inflammation was diagnosed histologically using criteria of myeloid cell/lymphocyte infiltration in tissues as described (25). Cases diagnosed with inflammatory conditions exhibited expansions of immature myeloid cells, monocytes and granulocytes in tissues outside the bone marrow and often in spleen or liver. Infections were diagnosed with evidence for bacterial or parasitic infection in different tissues, including visualization of bacteria and entamoeba as described (2628).

Individual mice could have more than one type of pathology. Examples include B cell lymphoma and lung inflammation, pancreatitis and hepatocellular adenoma, bacterial infection and hemorrhagic liver.