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Localization of mucosal mast cells in W/W V mice after reconstitution with bone marrow cells or cultured mast cells, and its relation to the protective capacity to Strongyloides ratti infection
Author(s) -
ABE T.,
NAWA Y.
Publication year - 1987
Publication title -
parasite immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.795
H-Index - 75
eISSN - 1365-3024
pISSN - 0141-9838
DOI - 10.1111/j.1365-3024.1987.tb00524.x
Subject(s) - mast cell , lamina propria , biology , bone marrow , crypt , immunology , epithelium , stem cell factor , intestinal epithelium , microbiology and biotechnology , pathology , stem cell , haematopoiesis , medicine , endocrinology , genetics
Summary Localization of mast cells in the intestinal epithelium, villous lamina propria and basal lamina propria of mast cell‐deficient WBB6F 1 (W/W v ) mice reconstituted with either bone marrow cells or with cultured mast cells (BMMC) was compared to that of mast cell‐sufficient C57 BL/6 or C57 BL/6‐bg j /bg j (beige) mice after infection with Strongyloides ratti. In mast cell‐sufficient C57 BL/6 or beige mice, the maximum number of intestinal mucosal mast cells (MMC) was more than 160 MMC/10 villus crypt units (VCU) and more than 90% of MMC were located in the intestinal epithelium. When W/W V mice were reconstituted with bone marrow cells of beige mice, worm expulsion was hastened and the MMC response became comparable to that of mast cell‐sufficient mice in terms of cell numbers and their intra‐epithelial localization. On the other hand, when W/W v mice were reconstituted with BMMC of beige mice, only a few donor type MMC were detected in the intestine. The proportion of intra‐epithelial MMC was lower than that of mast cell‐sufficient mice or of marrow‐reconstituted W/W v mice. Even repeated injection of BMMC could not fully restore the number of intra‐epithelial MMC to the level of that observed in mast cell‐sufficient mice. Since mast cell‐growth factor‐producing activity of W/W v mice was comparable to that of mast cell‐sufficient mice, the ineffectiveness of BMMC‐transfer in restoring protective activity or MMC responses in W/W V mice seems to be attributed to the functional immaturity or inactivity of BMMC.