Scanning electron microscopy of cultured human megakaryocytes. 1984

S Chen, and M I Barnhart

Human megakaryocytes (MK) from rib marrows of 16 patients with normal hematological patterns were isolated by Percoll density centrifugation followed by velocity sedimentation. The surface features of freshly isolated MK and the unseparated marrow suspensions were examined by SEM. A wide range of surface morphology for MK was noted depending on their size and maturation stages. Megakaryoblasts had a relatively smooth surface. During maturation, MK became villous and some had small blebs. In late maturation, many MK had complex surface processes including typical discs, slightly sphered projections, tear drop projections, putative sheet-like platelets or combinations of two or more of such surface features. Both unseparated and MK-rich fractions (F); specifically F1 lower, F2 lower and F3 were cultured up to 19 days. MK maintained their spherical shape in culture. At different time intervals (2, 5, 9 and 19 days), some cultures were terminated. MK retained their characteristic surface features. Promegakaryocytes and young adult MK were seen in short term cultures. The majority of cultured MK had platelet-like bodies on their surface in the prolonged cultures. Sometimes a few morphologically recognizable platelets were seen in the culture media. Differential counts of MK were done in all preparations of both unseparated and MK enriched fractions. F3, having no morphologically recognizable MK, had many MK present after culturing in vitro for 19 days. These MK had typical platelets or platelet-like processes on their surface. This suggests some MK progenitors originally present in the isolated F3 fraction became mature in cultures.

UI MeSH Term Description Entries
D008533 Megakaryocytes Very large BONE MARROW CELLS which release mature BLOOD PLATELETS. Megakaryocyte
D008855 Microscopy, Electron, Scanning Microscopy in which the object is examined directly by an electron beam scanning the specimen point-by-point. The image is constructed by detecting the products of specimen interactions that are projected above the plane of the sample, such as backscattered electrons. Although SCANNING TRANSMISSION ELECTRON MICROSCOPY also scans the specimen point by point with the electron beam, the image is constructed by detecting the electrons, or their interaction products that are transmitted through the sample plane, so that is a form of TRANSMISSION ELECTRON MICROSCOPY. Scanning Electron Microscopy,Electron Scanning Microscopy,Electron Microscopies, Scanning,Electron Microscopy, Scanning,Electron Scanning Microscopies,Microscopies, Electron Scanning,Microscopies, Scanning Electron,Microscopy, Electron Scanning,Microscopy, Scanning Electron,Scanning Electron Microscopies,Scanning Microscopies, Electron,Scanning Microscopy, Electron
D001853 Bone Marrow The soft tissue filling the cavities of bones. Bone marrow exists in two types, yellow and red. Yellow marrow is found in the large cavities of large bones and consists mostly of fat cells and a few primitive blood cells. Red marrow is a hematopoietic tissue and is the site of production of erythrocytes and granular leukocytes. Bone marrow is made up of a framework of connective tissue containing branching fibers with the frame being filled with marrow cells. Marrow,Red Marrow,Yellow Marrow,Marrow, Bone,Marrow, Red,Marrow, Yellow
D002469 Cell Separation Techniques for separating distinct populations of cells. Cell Isolation,Cell Segregation,Isolation, Cell,Cell Isolations,Cell Segregations,Cell Separations,Isolations, Cell,Segregation, Cell,Segregations, Cell,Separation, Cell,Separations, Cell
D002478 Cells, Cultured Cells propagated in vitro in special media conducive to their growth. Cultured cells are used to study developmental, morphologic, metabolic, physiologic, and genetic processes, among others. Cultured Cells,Cell, Cultured,Cultured Cell
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

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