Non-mammalian Erythrocytes Research Articles

Origins of the Vertebrate Erythro/Megakaryocytic System.

Vertebrate erythrocytes and thrombocytes arise from the common bipotent thrombocytic-erythroid progenitors (TEPs). Even though nonmammalian erythrocytes and thrombocytes are phenotypically very similar to each other, mammalian species have developed some key evolutionary improvements in the process of erythroid and thrombocytic differentiation, such as erythroid enucleation, megakaryocyte endoreduplication, and platelet formation. This brings up a few questions that we try to address in this review. Specifically, we describe the ontology of erythro-thrombopoiesis during adult hematopoiesis with focus on the phylogenetic origin of mammalian erythrocytes and thrombocytes (also termed platelets). Although the evolutionary relationship between mammalian and nonmammalian erythroid cells is clear, the appearance of mammalian megakaryocytes is less so. Here, we discuss recent data indicating that nonmammalian thrombocytes and megakaryocytes are homologs. Finally, we hypothesize that erythroid and thrombocytic differentiation evolved from a single ancestral lineage, which would explain the striking similarities between these cells.

The cytomorphic system of anucleate non-mammalian erythrocytes

Cytomorphic structure was studied in erythrocytes ofBatrachoseps salamanders, a genus unique among non-mammalian vertebrates because most of the erythrocytes are anucleate. These anucleate erythrocytes are highly flattened, quite variable in size, and generally elliptical. All of them were found to contain marginal bands of microtubules (MBs), as observed in phase contrast and darkfield after Triton lysis. The MBs of larger cells typically twisted into figure-8 forms upon lysis. Whole mounts of the lysed anucleate cells consisted only of the MB plus a trans-MB network of material (TBM), as observed by electron microscopy. If lysis was carried out in the presence of 0.5 M KCl, all of the MBs circularized immediately and none were twisted. The network (TBM) was now missing, suggesting that it is needed for maintenance of MB ellipticity and plays a role in MB twisting. Small numbers of living anucleate erythrocytes were constricted in their mid-region, and others were pointed at one end. Correspondingly pointed MBs were observed after lysis, exhibiting a range of forms compatible with the mechanism proposed byEmmel (1924) in which the anucleate erythrocytes arise by amitotic division of nucleated ones. The results show that these erythrocytes retain the typical nonmammalian cytomorphic system, and are thus unlike those of adult mammals. The network component (TBM) is present even though nuclei are absent, making it unlikely that it functions simply to position the nucleus. The observations are consistent with the hypothesis that the flattened, elliptical shape of non-mammalian vertebrate erythrocytes is generated by TBM tension applied across the faces of the MB “frame”, and that excessive tension induced by lysis (without KCl) produces MB twisting.

Failure of in vivo and in vitro resialosylation of VCN-desialylated erythrocytes in mammalian and non-mammalian species: Evidence from agglutination studies with peanut-agglutinin

1. 1. In distinction to mammalian erythrocytes, splitting of sialic acids of non-mammalian erythrocytes (chicken and newt) by Vibrio cholearae neuraminidase (VCN) does not lead to a dramatic decrease in their viability. 2. 2. One of the possibilities to explain this discrepancy is the ability of chicken and newt desialosylated erythrocytes to repair the enzymatic injury. 3. 3. To test this hypothesis we used the property of peanut agglutinin (PNA) to agglutinate desialosylated erythrocytes. 4. 4. Desialosylated erythrocytes of all the species tested remain PNA-agglutinable throughout their whole life time in the blood stream. The absence of effect of VCN on chicken and newt erythrocytes is therefore not due to their resialosylation.

Quantitation of cellular deoxyribonucleic acid by flow microfluorometry.

This report characterizes for the first time an easy, reproducible means of standardizing the relative fluorescent units normally reported for flow microfluorometry. Absolute values for deoxyribonucleic acid/cell are obtained by using nucleated red blood cells as references. Cell were selected and characterized for the quantitative analysis of deoxyribonucleic acid per cell over a range from 2 pg/cell to 93 pg/cell using literature values for species having nucleated erythrocytes. Fluorescence staining by either acridine-orange (green wavelength) or propidium iodide (red wavelength) gave linear curves over the entire range investigated only when "gain controls" and current are optimized. The range was equivalent to mammalian cell values from 1 N (=3.5 pg deoxyribonucleic acid/cell) to 28 N (=91 pg deoxyribonucleic acid/cell). The standard curves obtained with nonmammalian erythrocytes were compared to mammalian free-cell preparations of bovine thymus and liver cells which fell at 6.8 and 6.9 pg deoxyribonucleic acid/cell, respectively. The routine use of these easily obtainable red blood cells will allow ready comparisons on the basis of absolute values for deoxyribonucleic acid per cell for work between experiments, work between staining procedures and dye types and work between laboratories.