A potential role of the NOD genetic background in mouse peritoneal macrophages for the development of primary effusion lymphoma. (March 2016)

• Record Type: Journal Article
• Authors: Goto, Hiroki; Kariya, Ryusho; Matsuda, Kouki; Kudo, Eriko; Katano, Harutaka; Okada, Seiji
• Is Part Of: Leukemia research. Volume 42(2016:Mar.)
• Page Start: 37
• Page End: 42
• Publication Date: 2016-03
• Subjects: Immunodeficient mice -- Macrophage -- NOD -- Primary effusion lymphoma; Leukemia -- Periodicals; Leukemia -- Periodicals; Leucémie -- Périodiques; Leukemia; Periodicals; Electronic journals; Electronic journals; 616.9941905
• DOI: 10.1016/j.leukres.2016.01.011
• Languages: English
• ISSNs: 0145-2126

Abstract

Highlights: NOD mice macrophages phagocytosed PEL cells less efficiently than non-NOD macrophages. NOD background contributed to more PEL effusion than non-NOD background in vivo . Macrophages played a critical role in preventing the development of PEL. Abstract: Severe immunodeficient mice have become invaluable tools in human stem cell and tumor research. In this study, we compared the phagocytic activity of peritoneal macrophages against primary effusion lymphoma (PEL) among Rag-2/Jak3 double-deficient (Rag-2 −/− Jak3 −/− ) mice with NOD and non-NOD (Balb/c and C57/BL6). We also evaluated lymphomatous effusion and infiltration in a PEL xenograft mouse model using these severe immunodeficient mice. In the phagocytic assay, peritoneal macrophages in the NOD background phagocytosed CFSE-labeled BCBL-1, a PEL cell line, less efficiently than those in the non-NOD background. BCBL-1 cells were successfully engrafted into both the NOD background and non-NOD background; however, the volume of ascites of the NOD background was significantly higher than that of the non-NOD background. Moreover, the organ invasion of PEL cells was suppressed in non-NOD background mice. Thus, the NOD genetic background is considered to contribute to more lymphomatous effusion and the infiltration of PEL cells than a non-NOD background. Our results showed that the NOD background allowed more lymphomatous effusion and infiltration than other backgrounds and peritoneal macrophages played a critical role in preventing the growth and infiltration of PEL cells.