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Blood, 15 April 2008, Vol. 111, No. 8, pp. 3914-3915.
IL6 to the rescueUNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL
In addition to classic homeostatic granulocyte production mediated by G-CSF and GM-CSF, an independent pathway stimulated by IL6 complexed with its soluble receptor (sIL6R) contributes to emergency granulopoiesis.
Accordingly, double-knockout G-CSF–/–/GM-CSF–/– mice show pro-found defects in neutrophil production and function.2 However, when challenged with microbial pathogens, these mice respond with increased production of both myeloid precursors and mature neutrophils, indi-cating an alternative pathway of "emergency" granulopoiesis. In this issue of Blood, Walker and colleagues have identified IL6/sIL6R complexes as the mediators of this pathway in an in vitro model of emergency granulopoiesis in the absence of G-CSF and GM-CSF. In vivo experiments using triple-knockout G-CSF–/–/GM-CSF–/–/IL6–/– mice proved infeasible due to their poor viability. Therefore, the authors developed an in vitro culture system using colony formation from G-CSF–/–/GM-CSF–/– bone marrow as a bioassay for neutrophil-promoting activity in conditioned media from LPS-stimulated G-CSF–/–/GM-CSF–/– embryonic fibroblasts. Previous studies had indicated essential roles for IL6 and, surprisingly, M-CSF for this activity, but neither was sufficient. The present work has elucidated a multicomponent pathway in which binding of IL6 to the soluble form of its receptor produces a transstimulatory IL6/sIL6R complex. The requirement for M-CSF may reflect its amplification of IL6 secretion or augmentation of sIL6R release by protease cleavage of membrane-bound IL6 receptor (mIL6R). The primary limitation of this work, as the authors acknowledge, is the in vitro model system that proved essential for identification of the neutrophil-promoting complex, but which lacked proof of in vivo applicability. Due to the redundancy of cytokine controls for neutrophil production, future studies may more easily demonstrate that IL6/sIL6R complexes are sufficient rather than that they are necessary for emergency granulopoiesis in vivo. In the future, the physiological role of IL6/sIL6R complexes will undoubtedly be compared with that of IL6, the only form of the cytokine heretofore associated with hematopoiesis. IL6 directly binds to mIL6R, and the resultant multimer associates with the signal transduction protein gp130 (reviewed in Scheller et al3). mIL6R expression is limited to hepatocytes and some hematopoietic cells, but the ubiquitous expression of gp130, which also responds to IL6/sIL6R, renders nearly all cells potentially responsive to the IL6/sIL6R complex. mIL6R has been detected in myeloid progenitor cells in vitro, and increases with their differentiation.4 If its expression is dependent upon G-CSF or GM-CSF, then IL6/sIL6R would provide a bypass mechanism unique to double-knockout cells. However, the soluble complex could also represent an independent physiological signal to myeloid precursors from tissue stromal and immune cells encountering microbial pathogens. The current study helps to solve the mystery of the neutrophil response in double-knockout mice. Further studies must determine whether the pathway is a phenomenon of cell culture or an important emergency signal from infected or stressed tissue to the bone marrow.
Footnotes
Conflict-of-interest disclosure: The author declares no competing financial interests.
REFERENCES
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