Publication | Open Access
bcl-2 inhibits apoptosis of neutrophils but not their engulfment by macrophages.
282
Citations
30
References
1994
Year
Programmed DeathApoptosisImmunologyImmune RegulationCell DeathPathologyImmunotherapyCell Death MechanismsInflammationHematological MalignancyHematologyBcl-2 Inhibits ApoptosisMature NeutrophilsBone MarrowAutoimmune DiseaseGranulocyteAutoimmunityCell BiologyPhagocyteCytokineMalignant Blood DisorderMedicine
Neutrophils, the most common inflammatory leukocytes, have the most limited life span of all blood cells. After they undergo apoptosis, they are recognized and engulfed by macrophages. bcl-2, a proto-oncogene rearranged and deregulated in B cell lymphomas bearing the t(14;18) translocation, is known to inhibit programmed death. bcl-2 expression is localized in early myeloid cells of the bone marrow but is absent in mature neutrophils. Transgenic mice that expressed bcl-2 in mature neutrophils showed that bcl-2 blocked neutrophil apoptosis. Despite this, homeostasis of neutrophil population is essentially unaffected. In fact, macrophage uptake of neutrophils expressing bcl-2 still occurred. This transgenic model indicates that the mechanism that triggers phagocytosis of aging neutrophils operates independently of the process of apoptosis regulated by bcl-2.
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