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Further studies on the mechanism of marrow granulocytic hyperplasia in mice chronically injected with endotoxin
Author(s) -
Levitt Lee J.,
Quesenberry Peter J.
Publication year - 1982
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/j.1365-2141.1982.tb01917.x
Subject(s) - granulopoiesis , bone marrow , in vivo , hyperplasia , granulocyte , immunology , biology , colony stimulating factor , progenitor cell , endocrinology , medicine , haematopoiesis , stem cell , microbiology and biotechnology
Marrow granulocytic hyperplasia occurs regularly in mice injected with endotoxin for 7‐30 d, despite minimal elevations of serum colony‐stimulating activity (CSA). Alterations in marrow granulocyte‐monocyte progenitor (CFU‐C) number or changes in marrow cell cycle status do not explain this hyperplasia. We have studied other mechanisms which may explain this increased granulopoiesis. CF 1 , BDF 1 or C57bl/6J mice were injected with 10 μg of S. typhosa , endotoxin i.p. daily for 7‐20 d. Control and endotoxin injected (tolerant) sera, each with identical levels of CSA, were assayed against control marrow cells stimulated with supramaximal amounts of CSA to assess the role of serum potentiators in augmenting granulopoiesis. In six separate experiments, tolerant sera, over a 30‐fold concentration range, produced a 1.7–4.0‐fold potentiation of colony growth compared to control sera (P<0.001). No increased tolerant sera potentiation was seen over a similar concentration range when assayed against tolerant marrow. Tolerant and control splenic conditioned media, both dialysed and non‐dialysed, failed to potentiate control marrow colony growth. Tolerant marrow stem cells did not show changes in CSA sensitivity, colony size distribution or differentiation, and tolerant bone or bone marrow cells did not produce increased amounts of CSA. We conclude that serum factors separate from CSA may in part explain the increased granulopoiesis seen in endotoxin injected mice. The failure of tolerant sera to potentiate tolerant marrow growth in vitro , may reflect prior in vivo , exposure of marrow to these potentiating factor(s).