Processing and presentation of intact hen egg-white lysozyme by dendritic cells
β Scribed by Marloes L. H. De Bruijn; John D. Nieland; Clifford V. Harding; Cornelis J. M. Melief
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 754 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0014-2980
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β¦ Synopsis
Processing and presentation of intact hen egg-white lysozyme by dendritic cells* Dendritic cells in lymphoid tissues are of key importance as highly specialized antigen-presenting cells for the induction of T lymphocyte responses. Conflicting results have been published regarding antigen processing of intact proteins by dendritic cells. We now report that highly purified dendritic cells isolated from H-2k mouse spleens very efficiently generated immunogenic fragments of intact hen egg-white lysozyme (HEL) protein to present to an I-Ak-restricted T hybridoma cell line, specific for HEL peptide 46-61. Dendritic cells required 100 times less HEL protein than lipopolysaccharide-induced B cell blasts for effective presentation. Uptake of 1251-labeled HEL protein by dendritic cells and inhibition of presentation of HEL protein by chloroquine treatment was observed. This indicates an endocytotic process and the involvement of acidified compartments. Since the supernatant of dendritic cells, that were incubated with intact HEL protein, contained immunogenic fragments, further evidence for processing of HEL protein by dendritic cells was obtained. When HEL protein was covalently coupled to beads, dendritic cells were not able to ingest these beads, but could still process HEL protein for presentation. This suggests cell surface processing of HEL protein, although internalization of HEL protein released from the beads cannot be excluded.Taken together, these data show that H-2k dendritic cells are capable of processing and presenting intact HEL protein.
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The influence of the class II-associated invariant chain (Ii) on the presentation of the protein antigens hen egg-white lysozyme (HEL) and ribonuclease A (RNase) was investigated. For this purpose the Ii- rat-2 fibroblasts were transfected with I-Ak genes with or without Ii. Transfectants expressing
## Abstract Here we have studied the effects of apoptotic cell death induced by chemotherapic agents on tumor phagocytosis by dendritic cells (DC) and presentation of the relevant antigen to T lymphocytes. AnnexinβVβFITC (AnnβV) and propidium iodide (PI) staining was used to assess early apoptotic