Wick M J, Pfeifer J D, Findlay K A, Harding C V, Normark S J
Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri 63110.
Infect Immun. 1993 Nov;61(11):4848-56. doi: 10.1128/iai.61.11.4848-4856.1993.
The effect of abundance and compartmentalization of antigenic epitopes expressed in Escherichia coli on phagocytic processing was studied by expressing fusion proteins containing the epitope from positions 52 to 61 of hen egg white lysozyme [HEL(52-61)], which binds the I-Ak murine major histocompatibility complex class II (MHC-II) molecule or the epitope from positions 257 to 264 of chicken egg ovalbumin [OVA(257-264]), which binds the Kb murine MHC-I molecule. Epitopes expressed as fusion proteins in the outer membrane protein LamB allowed exposure of the epitopes either at the bacterial surface, in the periplasmic space, or in the cytoplasm. Regardless of epitope compartmentalization within the bacterium, MHC-II-restricted or MHC-I-restricted presentation to T hybridoma cells occurred after macrophages phagocytosed bacteria producing the HEL(52-61) epitope or the OVA(257-264) epitope, respectively. Increased epitope abundance within a given microbial compartment resulted in increased processing and presentation to epitope-specific T hybridoma cells. Minor differences in the efficiency of epitope processing between the constructs was observed, and the HEL or OVA epitope exposed in the periplasmic space was processed most efficiently compared with the surface- or cytoplasm-localized epitopes. These differences could be overcome by increasing the amount of epitope per bacterium as little as two to five times. The minor differences in processing efficiency may be due to differing protein contexts of the epitope as well as differing epitope compartmentalizations within the bacteria. Thus, production of abundant epitope is the important parameter influencing processing of epitopes expressed in E. coli to induce T-cell responses rather than targeting of an epitope to a specific bacterial compartment.
通过表达含有来自鸡蛋清溶菌酶[HEL(52 - 61)]第52至61位氨基酸的表位(其与I - Ak小鼠主要组织相容性复合体II类(MHC - II)分子结合)或来自鸡卵清蛋白[OVA(257 - 264)]第257至264位氨基酸的表位(其与Kb小鼠MHC - I分子结合)的融合蛋白,研究了在大肠杆菌中表达的抗原表位的丰度和区室化对吞噬处理的影响。以外膜蛋白LamB中的融合蛋白形式表达的表位可使表位暴露于细菌表面、周质空间或细胞质中。无论表位在细菌内的区室化情况如何,巨噬细胞吞噬产生HEL(52 - 61)表位或OVA(257 - 264)表位的细菌后,分别发生MHC - II限制或MHC - I限制的向T杂交瘤细胞的呈递。给定微生物区室内表位丰度的增加导致向表位特异性T杂交瘤细胞的处理和呈递增加。观察到构建体之间表位处理效率的微小差异,与表面或细胞质定位的表位相比,周质空间中暴露的HEL或OVA表位处理效率最高。将每个细菌的表位量增加至仅两到五倍即可克服这些差异。处理效率的微小差异可能是由于表位的不同蛋白质背景以及细菌内不同的表位区室化。因此,丰富表位的产生是影响大肠杆菌中表达的表位处理以诱导T细胞反应的重要参数,而不是将表位靶向特定的细菌区室。