1. Tubulin is retained throughout the human hematopoietic/erythroid cell differentiation process and plays a structural role in sedimentable fraction of mature erythrocytes.
- Author
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Nigra AD, Santander VS, Dircio-Maldonado R, Amaiden MR, Monesterolo NE, Flores-Guzmán P, Muhlberger T, Rivelli JF, Campetelli AN, Mayani H, and Casale CH
- Subjects
- Adult, Blood Sedimentation drug effects, Erythrocytes drug effects, Female, Humans, Male, Nocodazole pharmacology, Paclitaxel pharmacology, Spectrin metabolism, Tubulin chemistry, Erythrocytes cytology, Erythrocytes metabolism, Hematopoiesis drug effects, Tubulin metabolism
- Abstract
We investigated the properties of tubulin present in the sedimentable fraction ("Sed-tub") of human erythrocytes, and tracked the location and organization of tubulin in various types of cells during the process of hematopoietic/erythroid differentiation. Sed-tub was sensitive to taxol/nocodazole (drugs that modify microtubule assembly/disassembly), but was organized as part of a protein network rather than in typical microtubule form. This network had a non-uniform "connected-ring" structure, with tubulin localized in the connection areas and associated with other proteins. When tubulin was eliminated from Sed-tub fraction, this connected-ring structure disappeared. Spectrin, a major protein component in Sed-tub fraction, formed a complex with tubulin. During hematopoietic differentiation, tubulin shifts from typical microtubule structure (in pro-erythroblasts) to a disorganized structure (in later stages), and is retained in reticulocytes following enucleation. Thus, tubulin is not completely lost when erythrocytes mature; it continues to play a structural role in the Sed-tub fraction., (Copyright © 2017 Elsevier Ltd. All rights reserved.)
- Published
- 2017
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