Methodologies and tools to shed light on erythrophagocytosis
Red blood cells (RBC) are the most abundant circulating cell of the human body. RBC are constantly exposed to multiple stresses in the circulation, leading to molecular and structural impairments and death. The physiological process of RBC senescence or ageing is referred to as eryptosis. At the end...
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Veröffentlicht in: | Biochimie 2022-11, Vol.202, p.166-179 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Red blood cells (RBC) are the most abundant circulating cell of the human body. RBC are constantly exposed to multiple stresses in the circulation, leading to molecular and structural impairments and death. The physiological process of RBC senescence or ageing is referred to as eryptosis. At the end of their lifespan, aged RBC are recognized and removed from the blood by professional phagocytes via a phenomenon called erythrophagocytosis (EP); the phagocytosis of RBC. Some genetic and acquired diseases can influence eryptosis, thereby affecting RBC lifespan and leading to hemolytic anemia. In some diseases, such as diabetes and atherosclerosis, eryptosis and EP can participate in disease progression with both professional and non-professional phagocytes. Therefore, investigating the process of EP in vivo and in vitro, as well as in different cell types, will not only contribute to the understanding of the physiological steps of EP, but also to the deciphering of the specific mechanisms involving RBC and EP that underlie certain pathologies. In this review, the process of EP is introduced and the different methods for studying EP are discussed together with examples of the experimental procedures and materials required.
•Erythrocytes are central players in the development and progression of atherosclerosis.•Erythrophagocytosis within the atherosclerotic plaque contributes to its rupture.•The study of erythrophagocytosis is important to decipher mechanisms involving erythrocytes.•This review highlights and describe the different methods for studying erythrophagocytosis. |
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ISSN: | 0300-9084 1638-6183 |
DOI: | 10.1016/j.biochi.2022.07.017 |