Tag Archives: pronormoblast

Morphology of Myeloid Precurssors

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The earliest morphologically distinct myeloid cell is a myeloblast. Cell with myeloid commitment at stages of differentiation between the pleuripotant stem cell and myeloblasts have been identified but these lack morphological characters of a myeloid lineage. Myeloid cells share a common precursors with the cells of the monocyte-macrophage system in the form of CFU-GM. CFU-GM matures into CFU-G, a precursor for myeloid cells and CFU-M, a precursor for cells of the monocyte-macrophage series. There are five morphological distinct stages of myeloid precursors, myeloblast, promyelocyte, myelocyte, metamyelocyte and the band form. Only the first three are capable of cell division. Myeloid cells in the peripheral blood are classified into neutrophils, eosinophils and basophils depending on the staining characteristics of the cytoplasmic granules. Morphological evidence of commitment one of the myeloid lines is seen at the myelocyte stage. Electron microscopically commitment can be seen at the promyelocyte stage.

Figure 1. Myeloblast, Myelocyte and Metamyelocyte

Myeloblast (Figure 1, 3 and 4): Cells 10-20μ in size with a large slightly round nucleus with fine chromatin showing no clumping. Fine chromatin gives the nucleus a sieve-like or a finely granular appearance. The nucleus shows 2-5 pale sky-blue nucleoli. The nuclear membrane is exceedingly thin. Lymphoblasts nucleus may be differentiated from myeloblasts by the coarser chromatin, fewer nucleoli and the clumping of chromatin near the nuclear membranes. The cytoplasm of a myeloblast is basophilic but the basophilia is less marked than the lymphoblast or pronormoblast. Of the three types of leukaemic lymphoblasts the L1 (small cells with few nucleoli and a thin rim of cytoplasm) and L3 (strongly basophilic cytoplasm with prominent vacuolation) can be easily differentiated from myeloblasts morphologically. Differentiation of myeloblasts from L2 blasts on morphological grounds alone may not be possible. Perinuclear clearing is a feature of pronormoblasts and is not seen in the myeloblast. By definition myeloblasts have no granules but some classify cells with a few granules as myeloblasts particularly in the presence of abnormal myelopoiesis. In addition to granulation leukaemic myeloblasts may show nuclear furrows and Auer rods. Three stages in the maturation of myeloblasts are recognized

  1. Type I: No granules
  2. Type II: Fewer than 20 granules, Auer rods may be seen
  3. Type III: More than 20 granules seen without a Golgi apparatus

Very immature blasts lack morphological features of any lineage making it impossible to classify them as myeloblast, monoblast, lymphoblast or pronormoblast. Lineage identification in such cases may be aided by the company they keep, immunophenotyping and staining for peroxidase and esterases.

Figure 2. Promyelocytes

Promyelocyte (Figure 2): Slightly larger than a myeloblast (15-25μ), the promyelocyte is the largest cell of the myeloid series. Its nucleus is slightly indented, has a fine chromatin (though coarser than the myeloblast) and has nucleoli. Later stages show a slight chromatin condensation along the nuclear membrane. The cytoplasm is basophilic with prominent primary azurophilic granules. Endoplasmic reticulum is prominent and takes the form of dilated vesicles. Cells have a perinuclear Golgi apparatus that manifests as a perinuclear halo, but only in normal cells. Tough it is not possible to differentiate the promyelocytes of the three granulocytic (neutrophilic, basophilic, eosinophilic) series on light microscopy, electron microscopic difference exist. Leukaemic promyelocytes may be of the hypergranular or the hypogranular variety. The hypergranular variety has numerous small granules and Auer rods. Patients usually present with pancytopenia. Apart from having few or no granules in the cytoplasm the hypogranular variety may have a bilobed or folded nucleus.

Figure 3. Myelocytes – Neutrophilic, Eosinophilic and Basophilic

Myelocytes (Figure 1,3, 4 and 5): Lineage specific granules appear in the myelocyte stage. The cell is slightly smaller (10-20μ) than the promyelocyte and has an eccentric nucleus, round to oval, flattened on one side. Nucleoli are small and are only seen on EM, chromatin is coarse. Primary (azurophilic) granules persist but as no new granules are synthesized their number decreases with each division. The ratio of primary to secondary granules in a mature neutrophil is 2-3:1. Primary granules contain myeloperoxidase. The granulation of the endoplasmic reticulum is lesser than promyelocyte and as myelocytes mature the cytoplasmic basophilia decreases and finally disappears. The myelocyte may be neutrophilic, eosinophilic or basophilic. The granules of neutrophilic myelocytes are lilac, eosinophilic myelocytes are orange-red and basophilic myelocytes are purple. The eosinophilic myelocyte may contain purple staining granules. These are structurally different from granules of basophilic myelocytes. Myelocytes are the last stage to have the capacity to divide.

Granulocyte granules

Table 1. Charecteristics of granulocyte granules. The colour of the letters is the same as that of the granules and the backgroung the colour of cytoplasm of the cell the granules are most prominant in.

Figure 4. Myeloblast, Myelocyte and Eosinophil

Metamyelocyte (figure 1): Myelocytes matures to a metamyelocyte with appearance of nuclear indentation. Metamyelocyte can not divide. Unlike the transformation of a promyelocyte to a myelocyte that is accompanied by distinct morphological changes (disappearance of nucleoli, appearance of secondary granules) the most pronounced change that takes place when a myelocyte transforms into a metamyelocyte is indentation of the nucleus. Time-lapse photography has shown that the myelocyte nucleus can developed pronounced indentation and then revert to an oval shape. The distinction between the two stages is physiological. Metamyelocytes can not synthesize DNA, myelocytes can. Fortunately the distinction between a myelocyte and metamyelocyte is of little clinical importance and the ability of the cell to synthesize DNA is only assayed for research.

Band and Segmented Granulocytes (Figure 3): The indentation of the nucleus characteristic of the metamyelocyte increases and the nucleus becomes ribbon shaped. The nucleus of this cell has parallel borders for most of its length, like a band, and the cell is thus known as the band form. As the cell matures the nucleus becomes segmented. The segments are connected by thin strands of nuclear material. A constriction of more than half or two-third is accepted as segmentation by some. Neutrophils usually have 2-5 segments and eosinophils usually have 2 segments. Segmentations of the basophil nucleus are obscured by the intensely granular cytoplasm. The basophil nucleus ahs 2-3 segments, appearing in the contain few granules

Figure 5. Basophilic Myelocyte and Metamyelocyte

Morphological Characteristics of Myeloid Precursors

Cell Size Nucleus Cytoplasm
Myeloblast 12-20μ Round, fine chromatin, nucleoli Blue usually without granules. Some azurophilic granules may be present
Promyelocyte 15-25μ Slightly indented nucleus often eccentrically placed. Chromatin coarser than a myeloblast. Nucleoli seen Blue cytoplasm with numerous azurophilic granules
Myelocyte 10-20μ Round to oval, indented, chromatin more coarse than promyelocyte, no nucleoli Most immature forms have less basophilia than the promyeloblast. Basophilia disappeaqs as cell matures. Secondary granules appear.
Metamyelocyte 12-18μ Indented, coarse clumped chromatin Pink with secondary granules.
Band Form 10-12μ Band shaped. Borders are parallel for most of the length. May be folded Pink with secondary granules

Morphology of Erythroid Precursors

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Figure 1. Maturation of erythroid cells in the bone marrow

Pleuripotent stem cells give rise to erythrocytes by the process of erythropoiesis. The stem cell looks like a small lymphocyte and lacks the functional capabilities of the erythrocyte. The stem cells have the capacity of infinite division something the mature cells lack. Some of the daughter cells arising from the stem cell acquire erythroid characters over generations and time. Most of the erythroid cells in the bone marrow have a distinct morphology but commitment to erythroid maturation is seen even in cells that have not acquired morphological features distinctive of the erythroid lineage. These cells are recognized by the type of colonies they form in vitro. Two such cells are recognized. Burst-forming unit erythroid (BFU-E) arise from the stem cell and gives rise to colony-forming unit erythroid (CFU-E). CFU-E gives rise to pronormoblast, the most immature of erythroid cells with a distinct morphology (figure 1). BFU-E and CFU-E form a very small fraction of bone marrow cells and are not important in diagnosis. Examination of Romanovsky stained (Giemsa, Wright’s) bone marrow smears is central to the haematological diagnosis. Morphologically five erythroid precursors are identifiable in the bone marrow stained with Romanovsky stains. The five stages from the most immature to the most mature are the proerythroblast, the basophilic normoblast (early erythroblast), polychromatophilic normoblast (intermediate erythroblast), orthochromatophilic normoblast (late erythroblast) and reticulocyte (figure 1). As the cell matures the following morphological changes take place

  1. Cell becomes smaller
  2. Nucleus becomes smaller, chromatin more clumped and the nucleoli disappear
  3. Cytoplasm shrinks
  4. The cytoplasmic basophilia decreases: Haemoglobin is a major constituent of the red cell takes a pink to red colour on staining with Romanovsky stains. The machinery to synthesize haemoglobin (ribosomes) must appear before haemoglobin. Ribosomes make the cytoplasm basophilic (blue) because of their RNA content. As the haemoglobin content approaches the desired levels the number of ribosomes decreases. The cytoplasm of the maturing erythroid cell captures these changes and changes from deep blue (mainly ribosomes) in basophilic normoblast to polychromatophilic (ribosomes and haemoglobin) in polychromatophilic normoblast and resembling that of a erythrocyte (mainly haemoglobin) in orthochromatophilic normoblast.
  5. The earliest nucleated stages are least numerous and the later stages the most numerous

Figure 2. Proerythroblasts. The nucleus has multiple nucleoli a feature that distinguishes this stage.

Proerythroblast: Proerythroblast (figure 2) is a large cell (12-20μm in size or about 1.5-3 times a normal erythrocyte) with a large nucleus that occupies almost 80% of the cell and a blue cytoplasm that forms a thin rim around the nucleus. The chromatin is finely granular and stripped. The nucleus shows multiple nucleoli (the multiple pale staining areas in the nucleus). The cytoplasm may show a small pale area that corresponds to the Golgi apparatus and may have a pale perinuclear halo. While it is usually possible to tell a proerythroblast from other blasts (myeloblasts, lymphoblasts and monoblasts) by it’s more homgenous of cytoplasm, larger size ,a chromatin that coarser and the perinuclear halo in very immature cells this distinction may be impossible.

Figure 3. Basophilic Normoblasts. All four cells have basophilic cytoplasm but lack nucleoli. Nucleoli are a feature of proerythroblasts. Out of the four cells seen the two on the left are larger, have a less clumped chromatin. The cytoplasm of all four cells shows no polychromasia.

Basophilic Normoblast: The basophilic normoblast (figure 3, 4 and 5) is a smaller (12-17μm) cell. The nucleus is round like that of a proerythroblast but lacks nucleoli. Condensation of chromatin with the appearance of heterochromatin begins at this stage giving the nucleus a coarse and granular appearance. The number of ribosomes peak at in basophilic normoblasts and this reflects in the cytoplasmic colour. The basophilic normoblast has one of the bluest cytoplasm amongst the bone marrow cells. It may have a perinuclear halo. The nucleus may assume a wheel spoke arrangement like a plasma cell. The spoke wheel arrangement, the blue cytoplasm and similar size makes the basophilic normoblast resemble a plasma cell (figure 4). The plasma cell is elliptical with an eccentric nucleus while the basophilic normoblast is round with a central nucleus.

Figure 4. A basophilic normoblast (1) with a polychromatophilic normoblast (2) which is smaller with a cytoplasm more like a mature erythrocyte and a nuclear chromatin that is more clumped

Figure 5. A basophilic normoblast with two plasm cells. The plasma cells have an eccentric nucleus and are elliptical

Polychoromatophilic Normoblast: The polychromatophilic normoblast (figure 4) is a smaller (12-15μm). The distinguishing feature of this stage is the appearance of haemoglobin which reduces the basophilia of the cytoplasm. The chromatin shows a greater degree of clumping and irregular dense areas of staining are seen in the nucleus. Nucleoli are nor seen. Figure 4 shows adjacent basophilic and polychromatophilic normoblasts to contrast the size, the clumping of the chromatin and cytoplasmic staining (see normoblast maturation for more images of maturing polychromatophilic normoblasts).

Figure 6. Orthochromatophilic Normoblast. The cell slightly larger than an erythrocyte, nucleus is condensed and the cytoplasm is almost the colour of the erythrocyte

Orthochromaphilic Normoblast: The process of haemoglobinization is almost complete by the stage of orthochromatophilic normoblast (figure 6). “Ortho-” in Greek means straight, upright or correct. Though orthochromatophilic suggests that the colour of the cytoplasm is the same as mature erythrocyte, this is not the case. The orthochromatophilic normoblast is the nucleated erythroid precursor that is closest to a mature erythrocyte in terms of size (8-12μm) and cytoplasmic staining. The cytoplasm however retains a blue tinge much like a reticulocyte. The nucleus is greatly condensed, shrunk and assumes a variety of bizarre shapes (buds, clover leaves, double spheres). The chromatin is greatly condensed and almost completely homogenous.

Figure 7. The Reticulocyte. Reticulocytes (blue arrows) are larger than the normal erythrocytes. Some

Reticulocyte: The Orthochromatophilic normoblasts finally extrudes the nucleus and reticulocyte (figure 7)is formed. The reticulocyte is about 20% larger (7-9μm) than the mature erythrocyte. The lifespan of the reticulocyte is about 3 days. It spends 2 of these in the bone marrow. A day after appearing in the peripheral blood the reticulocyte looses the blue colour and becomes a erythrocyte.

Table 1. The summary of morphological features of erythroid cells
Cell Size Nucleus Cytoplasm
BFU-E, CFU-E The two cells are indistingushible from blasts of other series. They posses no morphological characters that indicates their erythroid origin
Pronormoblast 12-20 μ Fine chromatin, many nucleoli Blue, a perinuclear halo and a small pale area (Golgi apparatus) may be seen
Basophilic Normoblast 12-17 μ Granular chromatin, no nucleoli Very deep blue, perinuclear halo may be seen.
Polychromatophilic Normoblast 12-15 μ Cromatin is visibly clumped with dark staining areas Basophilia reduced but still not as pink as an erythrocyte
Orthochromatophilic normoblast 8-12 μ A featureless nucleus with dense chromatin Almost the colour of a reticulocyte
Reticulocyte 7-9μ No Nucleus Slightly blue compared to an erythrocyte
The nucleus of the small lymphocyte and the normoblast are about 7.5μ
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