## Abstract The high number (>10^8–10^) of primary human pro‐erythroblasts (CD36^high^/CD235a^low^) obtainable in HEMA culture (Migliaccio et al., 2002) is exploited here to analyse the expression of proteins implicated in erythropoietin (EPO)‐signalling (STATs, PI‐3K, and PLCs) during the process
Changes in the Expression of Membrane Antigens During the Differentiation of Chicken Erythroblasts
✍ Scribed by Michael J. Hayman; Hartmut Beug; Keith W. Savin
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 670 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0730-2312
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Chicken erythroblasts can be transformed by the avian retrovirus, avian erythroblastosis virus (AEV). Earlier studies have shown that the mechanism of transformation appears to involve a “block” in differentiation, in that when erythroblasts are transformed by a temperature‐sensitive mutant of __ts__34 AEV and incubated at the nonpermissive temperature, the cells start to differentiate and produce hemoglobin. We have decided to use this system to isolate pure populations of chicken erythroblasts and raise monoclonal antibodies against their cell surface proteins. Three monoclonal antibodies were isolated and tested for their ability to bind to various hematopoietic cell types; two were shown to be erythroid‐specific, whereas the other antibody bound to proliferating cells but not to erythrocytes or granulocytes. Of the erythroid‐specific antibodies, one precipitated a 94,000 molecular weight protein, whereas the other precipitated a 11,000 molecular weight protein that was tentatively identified as hemoglobin. The use of this system and approach to identify and evaluate changes that occur during the differentiation is discussed.
📜 SIMILAR VOLUMES
## Abstract In chickens, as in all vertebrates, tissue‐specific expression of aldolase isozymes A, B, and C is developmentally coordinated. These developmental transitions in aldolase expression have been studied most extensively by charting enzyme activity during normal and abnormal development of
## Abstract Erythrocyte membrane antigens have been detected on induced Friend erythroleukemic cells with a rabbit antiserum raised against mouse erythrocyte membranes. The antibody specificities of this antiserum have been quantitatively analyzed using a cellular radioimmunoassay. After absorption
Changes in the expression of a cell membrane antigen during hepatocarcinogenesis and In the developing liver were analyzed by HAM.4, a monoclonal antibody (MAb) against a membrane glycoprotein of normal rat hepatocyte. Of the precancerous lesions observed during hepatocarcinogenesis induced by dieth
## Abstract Spatial and temporal control of intracellular calcium signaling is essential for neuronal development and function. The termination of local Ca^2+^ signaling and the maintenance of basal Ca^2+^ levels require specific extrusion systems in the plasma membrane. In rat hippocampal neurons
## Abstract Chicken fetal antigen (CFA) describes a membrane developmental antigen system present on embryonic and fetal erythroid cells that is present during development, but is absent on erythrocytes of mature chickens. In this study, CFA was detected by indirect immunofluorescence and correlate