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Biomedical subjects

G A ACKERMAN

Publications and source records attributed to G A ACKERMAN.

At least 19 recordsLinked to original sources
PubMed1962

Electron microscopy of the bursa of Fabricius of the embryonic chick with particular reference to the lympho-epithelial nodules.

Electron microscopic studies of the bursa of Fabricius during the 15th and 16th day of embryonic development in the chick have shown the following findings in the submicroscopic structure of the cellular elements of the lympho-epithelial follicles. In the medulla, basal endodermal epithelial cells undergo mitosis and differentiation into lymphoblasts. During this transformation, there is a reduction in the amount of rough endoplasmic reticulum, an increase in the number or ribosomes, and frequently an enlargement of the Golgi complex. As lymphoblasts differentiate into medium lymphocytes there is a loss of endoplasmic reticulum, a reduction in the number of ribosomes and in the size of the Golgi complex, as well as a decrease in the number and size of mitochondria and in the size of the cell and nucleus. Cytoplasmic processes of reticular-epithelial cells extend between proliferating lymphocytic cells. Desmosomes connect stellate reticular-epithelial and basal epithelial cells but are not present in lymphocytic cells. Nuclear blebbing and vesiculation are frequently observed in the various cell forms of the developing lympho-epithelial nodules. Although lymphocytes and lymphocytopoietic activities in the cortex are sparse during this stage of embryonic development of the bursa, transitional forms between mesenchymal cells and lymphoblasts have been encountered. In addition, lymphoblasts and/or undifferentiated epithelial cells occasionally may pass through the basement membrane from the medulla into the cortical region of the developing nodule. That lymphocytes in the bursa of Fabricius originate from both endodermal and mesodermal derivatives during embryonic development appears to be consistent with both light and electron microscopic observations.

Animals↗
PubMed1962

Observations on the development of erythrocytes in mammalian fetal liver.

The fine structure of the erythrocyte during development in rabbit and human fetal liver has been studied. A morphologic description of representative erythropoietic cells and their relationship to the hepatic parenchyma is presented. Erythrocyte development was accompanied by a decrease in nuclear and cell size, fragmentation and eventual loss of nucleoli, and progressive clumping of chromatin at the nuclear margin. Mitochondria, endoplasmic reticulum, and Golgi elements decreased in size or abundance and eventually disappeared. Ribosome concentration initially increased, but subsequently diminished as the cytoplasm increased in electron opacity, probably through the accumulation of hemoglobin. Similar dense material, interpreted to be hemoglobin, infiltrated the nuclear annuli and, in some cases, appeared to extend into the interchromatin regions. There was a marked decrease in the number of annuli of the nuclear envelope. Possible relationships between nucleus and cytoplasm and of RNA to hemoglobin synthesis are discussed. In rabbits, erythroid and hepatic cells were separated by a 200 to 400 A space limited by the undulatory membranes of the respective cells. Membranes of adjacent erythropoietic cells were parallel and more closely apposed (100 to 200 A). In humans, relationship between various cells exhibited wide variation. Ferritin particles were observed within forming and formed "rhopheocytotic" vesicles.

Animals↗
PubMed1960

Histochemical demonstration of dehydrogenase activity in the cells of normal human blood and bone marrow.

Endogenous and succinic dehydrogenase activity was demonstrated in the living cells of normal human blood and bone marrow using a buffered nitro BT-succinate incubating solution. With this technique dehydrogenase activity was localized primarily in the granular leukocytes and the sites of enzymatic activity appeared to be non-mitochondrial. The addition of a non-ionic surface active agent to the incubating solution resulted in marked differences in the cellular and intracellular localization of dehydrogenase activity. With this method it was possible to demonstrate dehydrogenase activity in the mitochondria of most of the formed elements of the blood and bone marrow, including developing granulocytes and erythroid cells, agranulocytes, and blood platelets. Mature erythrocytes also exhibited a minimal dehydrogenase reaction with this procedure. This investigation indicated that in order adequately to demonstrate and evaluate dehydrogenase activity in the cells of the blood and bone marrow it was necessary to have increased cellular and mitochondrial permeability, as well as partially viable cells with an intact dehydrogenase system.

Blood Cells↗