Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, Queensland, Australia.
Immunol Cell Biol. 2012 Oct;90(9):889-95. doi: 10.1038/icb.2012.24. Epub 2012 May 29.
The distribution and function of the C-type lectin Mincle has not previously been investigated in human cells, although mouse models have demonstrated a non-redundant role for Mincle in the host response to fungal infections. This study identified an unusual pattern of reciprocal expression of Mincle on peripheral blood monocytes or neutrophils isolated from the same donor. Expression on monocytes was inversely correlated with phagocytosis and yeast killing, but was necessary for the induction of inflammatory cytokines in response to ex vivo Candida challenge. In contrast, Mincle expression on neutrophils was associated with phagocytic and candidacidal potential of those cells. Candida challenge upregulated Mincle expression but only in Mincle+ cells. These data highlight species-specific differences between the regulation of Mincle expression in mouse and man. Reciprocal expression of Mincle modified the candidacidal potential of monocytes or neutrophils, suggesting it may also polarize the type of host response to fungal infection.
虽然小鼠模型已经证明了 Mincle 在宿主对真菌感染的反应中具有非冗余的作用,但此前尚未在人类细胞中研究过 C 型凝集素 Mincle 的分布和功能。本研究在同一供体分离的外周血单核细胞或中性粒细胞中鉴定出 Mincle 表达的一种不寻常的相互关系模式。单核细胞上的表达与吞噬作用和酵母杀伤呈负相关,但对于诱导对体外念珠菌挑战的炎症细胞因子是必需的。相比之下,中性粒细胞上的 Mincle 表达与这些细胞的吞噬作用和念珠菌杀伤能力相关。念珠菌挑战上调了 Mincle 的表达,但仅在 Mincle+细胞中。这些数据突出了小鼠和人类中 Mincle 表达调控的种间差异。Mincle 的相互表达改变了单核细胞或中性粒细胞的念珠菌杀伤能力,表明它也可能使宿主对真菌感染的反应类型发生极化。