By Klaus Ley (auth.), Klaus Ley M.D. (eds.)
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Extra info for Physiology of Inflammation
1997). , 1998). , 1990). However, antibody studies can be confounded by toxicity or other effects of the antibody itself, and the relevance of in vitro assays to in vivo biology must of course always be tested. Indeed, in the case of CD44, data from work done with knockout mice are not easily reconciled with the in vitro data. , 1997), and reduced CFU-GM activity in the blood and spleen. If CD44 were required for myelopoiesis, as the in vitro data suggested, one would not expect elevated CFU-GM in the bone marrow of CD44 null animals.
A full review of the often-overlapping effects of these factors will not be attempted here, but is useful to try to place them in a conceptual framework. As discussed previously, some factors, such as SIF, TPO, and FL appear to affect HSC, directly or indirectly. Other, "late-acting" factors function in a lineage-specific manner on progenitors that are already committed to a lineage (for review, see Ogawa, 1993). G-CSF, among other functions, regulates proliferation and maturation of neutrophil precursors.
1996). In addition, although u 4 null T cells were able to migrate normally to lymph nodes, they were unable to colonize the Peyer's patches. Although NK cells and monocytes developed normally in the absence of u 4 integrin expression, B-cell development in the bone marrow of adult mice was blocked at an early stage. , 1996). , (1996) demonstrated that in the case of immigration of CD4 + CD3- cells into developing lymph nodes, alterations in interactions between adhesion molecules and their ligands can function as "developmen- Formation and Differentiation of Leukocytes 25 tal switches" by facilitating a function only in a specific window of time.
Physiology of Inflammation by Klaus Ley (auth.), Klaus Ley M.D. (eds.)