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Granulopoiesis

A single common myeloid progenitor differentiates into all of the hemopoietic cell lines, with the exception of lymphocytes (Fig. 1.1, Chapter 1. Erythrocytes). The bone marrow is the most effective and common site for hemopoiesis, including leukocyte production, in domestic animals. However, extramedullary production can also occur in other organs, such as the spleen and liver.

The production of granulocytes from bone marrow stem cells through to mature neutrophils, eosinophils, and basophils is known as granulopoiesis. Granulocytes are mobile leukocytes with the ability to phagocytose, degrade, and/or kill microorganisms, depending on the offending agent and granulocyte lineage.The commitment to neutrophilic, eosinophilic, or basophilic leukocytes occurs at an early level of common myeloid progenitor differentiation and is dependent on the presence and relative concentrations of several growth factors and cytokines. The most important of these are granulocyte-colony stimulating factor (G-CSF) for neutrophils; interleukin(IL)-5 for eosinophils; and stem cell factor (SCF) for basophils.

The earliest committed granulocyte precursor that can be recognized by light microscopy is the myeloblast (see Chapter 3. Hemopoietic Neoplasia, Fig. 3.8). Myeloblasts are agranular primitive cells which differentiate to promyelocytes with the synthesis of primary (azurophilic) granules. Primary granule contents include myeloperoxidase, lysozyme, and defensins. Synthesis of secondary (specific) granules defines the developing granulocyte as a neutrophilic, eosinophilic, or basophilic myelocyte. Secondary neutrophilic granule contents include lysozyme, lactoferrin, and gelatinase which, together with cytoplasmic organelles, enable phagocytosis and killing of microbes. Up to five mitotic divisions occur from myeloblast to myelocyte stages, and the total time in the mitotic (proliferating) phase of granulopoiesis is about 3 days. The post-mitotic (maturation and storage) phase comprises metamyelocytes, bands, and mature granulocytes. The interval from metamyelocyte to mature segmented granulocyte is also about 3 days for most animals (Fig. 2.1).

Figure 2.1 Neutrophil kinetics in health. The committed neutrophil precursor differentiates to the myeloblast which divides and differentiates to a mature neutrophil. Myeloblast to myelocyte represents the mitotic (proliferating) neutrophil pool, and metamyelocyte to mature neutrophil represents the post-mitotic (maturation and storage) neutrophil pool. In health, the total time in the mitotic phase is about 3 days. The interval from metamyelocyte to mature neutrophil in the post-mitotic phase is also about 3 days, in most animals. Peripheral blood neutrophils are in either the circulating pool (free in the circulation) or marginating pool (shown bound to receptors on the vascular endothelium). The marginating pool is positioned to migrate into tissues as required. Blood is collected by venipuncture from the circulating neutrophil pool. (Courtesy of Dr. Juliane Deubner, Medical Illustrator, Western College of Veterinary Medicine, University of Saskatchewan.)
Figure 2.1 Neutrophil kinetics in health. The committed neutrophil precursor differentiates to the myeloblast which divides and differentiates to a mature neutrophil. Myeloblast to myelocyte represents the mitotic (proliferating) neutrophil pool, and metamyelocyte to mature neutrophil represents the post-mitotic (maturation and storage) neutrophil pool. In health, the total time in the mitotic phase is about 3 days. The interval from metamyelocyte to mature neutrophil in the post-mitotic phase is also about 3 days, in most animals. Peripheral blood neutrophils are in either the circulating pool (free in the circulation) or marginating pool (shown bound to receptors on the vascular endothelium). The marginating pool is positioned to migrate into tissues as required. Blood is collected by venipuncture from the circulating neutrophil pool. (Courtesy of Dr. Juliane Deubner, Medical Illustrator, Western College of Veterinary Medicine, University of Saskatchewan.)
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Veterinary Clinical Pathology: An Introduction Copyright © by Marion Jackson; Beverly Kidney; and Nicole Fernandez is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, except where otherwise noted.