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Blood, 1 February 2004, Vol. 103, No. 3, pp. 1050-1058.
Prepublished online as a Blood First Edition Paper on October 2, 2003; DOI 10.1182/blood-2003-03-0707.
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NEOPLASIA
Lymphodepletion in the ApcMin/+ mouse model of intestinal tumorigenesis
P. Louise Coletta,
Albrecht M. Müller,
Elena A. Jones,
Bettina Mühl,
Sarah Holwell,
Deborah Clarke,
Josephine L. Meade,
Graham P. Cook,
Gillian Hawcroft,
Frederique Ponchel,
Wai K. Lam,
Ken A. MacLennan,
Mark A. Hull,
Constanze Bonifer, and
Alexander F. Markham
From the Molecular Medicine Unit, University of Leeds, Clinical Sciences Building, St James's University Hospital, Leeds, United Kingdom; and Institüt für Medizinische Strahlenkunde und Zellforschung (MSZ), Universität Würzburg, Würzburg, Germany.
Germ line mutations in the Adenomatous polyposis coli tumor suppressor gene cause a hereditary form of intestinal tumorigenesis in both mice and man. Here we show that in ApcMin/+ mice, which carry a heterozygous germ line mutation at codon 850 of Apc, there is progressive loss of immature and mature thymocytes from approximately 80 days of age with complete regression of the thymus by 120 days. In addition, ApcMin/+ mice show parallel depletion of splenic natural killer (NK) cells, immature B cells, and B progenitor cells in bone marrow due to complete loss of interleukin 7 (IL-7)-dependent B-cell progenitors. Using bone marrow transplantation experiments into wild-type recipients, we have shown that the capacity of transplanted ApcMin/+ bone marrow cells for T- and B-cell development appears normal. In contrast, although the ApcMin/+ bone marrow microenvironment supported short-term reconstitution with wild-type bone marrow, ApcMin/+ animals that received transplants subsequently underwent lymphodepletion. Fibroblast colony-forming unit (CFU-F) colony assays revealed a significant reduction in colony-forming mesenchymal progenitor cells in the bone marrow of ApcMin/+ mice compared with wild-type animals prior to the onset of lymphodepletion. This suggests that an altered bone marrow microenvironment may account for the selective lymphocyte depletion observed in this model of familial adenomatous polyposis. (Blood. 2004;103:1050-1058)

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