Evidence for Increased Proteolysis in Intact β Thalassemia Erythroid Cells
- 1 January 1981
- journal article
- research article
- Published by Taylor & Francis in Hemoglobin
- Vol. 5 (6) , 549-564
- https://doi.org/10.3109/03630268108991686
Abstract
Mxh excess u chain is synthesized, but little accumlates in the erythroid ells of patients with hanozycpus B thalassda. To dew if the proteases Imam to exist in erythmid cells play a role in the destruction or alteration of any of this excess α dmin, thalassemic and nmthalassemic erythroid cells were incubated for 90 minutes with 3H-leucine. The cells wxe then washed, and incubated Wioe for 15 minutes in 100 volunes of add leucine-rich media, a pmcedure which eliminates alrost all intracœllular TCA soluble radioadety. After these incubations levels of TCA soluble and TCA precipitable radioactivity in the cell lysates were detmdmdI and cells incubated for 120 minutes move in tm volumes of Ieucinerich media. At the end of this incubation, total Kl soluble and precipitable radioactivity was again determiraed in the œll lysate, and also in the tm hour incubaticn media. Tb total increase in TCA soluble radioactivity in the ells and their media was divided by the 0 time TCA precipitable radioactivity, to detadne the percmt proteolysis labelled globin chains. In five mtml patients Perœnt proteolysis ranged from 0 to 3.10 (* = 1.50); in four sewre and three mild thalassemia patients percent pmteolysis ranged fran 5.80 to 14.1 (X = 11.0). The difference between the control and thalassemia groups was significant at ap of <0.002. This data is the first direct evidence that more proteolysis takes place in intact thalassemia œlls than in non-thalassemia cells.This publication has 12 references indexed in Scilit:
- PROTEOLYSIS IN THALASSEMIA: STUDIES WITH PROTEASE INHIBITORS*Annals of the New York Academy of Sciences, 1980
- Protease activity in the human erythrocyte: localization to the cell membraneBlood, 1979
- Proteolytic activity in erythrocyte precursorsProceedings of the National Academy of Sciences, 1978
- A soluble ATP-dependent proteolytic system responsible for the degradation of abnormal proteins in reticulocytes.Proceedings of the National Academy of Sciences, 1977
- Role of the intrinsic transglutaminase in the Ca2+-mediated crosslinking of erythrocyte proteins.Proceedings of the National Academy of Sciences, 1976
- A kinetic study in vitro of the reoxidation of interchain disulfide bonds in a human immunoglobulin IgGLk. Correlation between sulfhydryl disappearance and intermediates in covalent assembly of H2L2.Proceedings of the National Academy of Sciences, 1975
- Intracellular Loss of Free α Chains in β ThalassaemiaNature, 1969
- The Pattern of Disordered Haemoglobin Synthesis in Homozygous and Heterozygous β-ThalassaemiaBritish Journal of Haematology, 1969
- Excess α Chain Synthesis Relative to β Chain Synthesis in Thalassaemia Major and MinorNature, 1966
- Peptide analysis of the inclusions of erythroid cells in β-thalassemiaBiochimica et Biophysica Acta (BBA) - General Subjects, 1966