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PGD2 and CRTH2 counteract Type 2 cytokine-elicited intestinal epithelial responses during helminth infection.PGD2 和 CRTH2 可拮抗寄生虫感染期间 2 型细胞因子诱导的肠道上皮细胞反应。
J Exp Med. 2021 Sep 6;218(9). doi: 10.1084/jem.20202178. Epub 2021 Jul 20.
2
Succinate Produced by Intestinal Microbes Promotes Specification of Tuft Cells to Suppress Ileal Inflammation.肠道微生物产生的琥珀酸促进肠绒毛细胞的特化以抑制回肠炎症。
Gastroenterology. 2020 Dec;159(6):2101-2115.e5. doi: 10.1053/j.gastro.2020.08.029. Epub 2020 Aug 21.
3
Tuft-Cell-Derived Leukotrienes Drive Rapid Anti-helminth Immunity in the Small Intestine but Are Dispensable for Anti-protist Immunity.簇细胞衍生的白三烯在小肠中迅速引发抗寄生虫免疫,但对抗原生动物免疫不是必需的。
Immunity. 2020 Mar 17;52(3):528-541.e7. doi: 10.1016/j.immuni.2020.02.005. Epub 2020 Mar 10.
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The Taste Receptor TAS1R3 Regulates Small Intestinal Tuft Cell Homeostasis.味觉受体TAS1R3调节小肠簇状细胞内环境稳定。
Immunohorizons. 2020 Jan 24;4(1):23-32. doi: 10.4049/immunohorizons.1900099.
5
Distribution pattern and molecular signature of cholinergic tuft cells in human gastro-intestinal and pancreatic-biliary tract.人类胃肠胰胆道胆碱能簇细胞的分布模式和分子特征。
Sci Rep. 2019 Nov 25;9(1):17466. doi: 10.1038/s41598-019-53997-3.
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Single-cell transcriptome analysis reveals differential nutrient absorption functions in human intestine.单细胞转录组分析揭示了人类肠道中不同的营养吸收功能。
J Exp Med. 2020 Feb 3;217(2). doi: 10.1084/jem.20191130.
7
Regulation of immune responses by tuft cells.被毛细胞调节免疫反应。
Nat Rev Immunol. 2019 Sep;19(9):584-593. doi: 10.1038/s41577-019-0176-x.
8
Schistosome Egg Migration: Mechanisms, Pathogenesis and Host Immune Responses.血吸虫卵迁移:机制、发病机制和宿主免疫反应。
Front Immunol. 2018 Dec 20;9:3042. doi: 10.3389/fimmu.2018.03042. eCollection 2018.
9
Schistosoma "Eggs-Iting" the Host: Granuloma Formation and Egg Excretion.血吸虫“鸡蛋-激动人心”宿主:肉芽肿形成和卵排泄。
Front Immunol. 2018 Oct 29;9:2492. doi: 10.3389/fimmu.2018.02492. eCollection 2018.
10
Schistosomiasis.血吸虫病。
Nat Rev Dis Primers. 2018 Aug 9;4(1):13. doi: 10.1038/s41572-018-0013-8.

慢性血吸虫病期间人大肠杯状细胞和微绒毛细胞的丰度和形态。

The abundance and morphology of human large intestinal goblet and tuft cells during chronic schistosomiasis.

机构信息

Department of Pathology, Stanford University School of Medicine, Palo Alto, California, USA.

Department of Microbiology and Immunology, Stanford University School of Medicine, Palo Alto, California, USA.

出版信息

Parasite Immunol. 2023 Jun;45(6):e12981. doi: 10.1111/pim.12981. Epub 2023 Apr 11.

DOI:10.1111/pim.12981
PMID:37038837
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10192203/
Abstract

Schistosomiasis affects nearly 240 million people in predominately low- and middle-income countries and ranks second in the number of cases and socio-economic burden among all parasitic diseases. Despite the enormous burden posed by schistosomes, our understanding of how schistosomiasis impacts infected human tissues remains limited. Intestinal schistosomiasis in animal models leads to goblet cell hyperplasia, likely increasing mucus production and reflecting an intestinal type 2 immune response. However, it is unknown whether these same changes occur in schistosome-infected humans. Using immunofluorescence and light microscopy, we compared the abundance and morphology of goblet cells in patients diagnosed with schistosomiasis to uninfected controls. The mucin-containing vesicles in goblet cells from schistosome-infected patients were significantly larger (hypertrophic) than uninfected individuals, although goblet cell hyperplasia was absent in chronic human schistosomiasis. In addition, we examined tuft cells in the large intestinal epithelium of control and schistosome-infected patients. Tuft cell numbers expand during helminth infection in mice, but these cells have not been characterized in human parasite infections. We found no evidence of tuft cell hyperplasia during human schistosome infection. Thus, our study provides novel insight into schistosome-associated changes to the intestinal epithelium in humans, suggesting an increase in mucus production by large intestinal goblet cells but relatively minor effects on tuft cell numbers.

摘要

血吸虫病影响着全球近 2.4 亿人口,主要集中在中低收入国家,在所有寄生虫病中,其病例数和社会经济负担均位居第二。尽管血吸虫对人类造成了巨大的负担,但我们对血吸虫病如何影响受感染的人体组织仍然知之甚少。动物模型中的肠道血吸虫病可导致杯状细胞增生,这可能增加了黏液的产生,并反映了肠道 2 型免疫反应。然而,目前尚不清楚这些相同的变化是否发生在受感染的人类身上。我们通过免疫荧光和光学显微镜,比较了诊断为血吸虫病的患者和未感染对照者的杯状细胞数量和形态。与未感染个体相比,来自血吸虫感染患者的杯状细胞中含有黏液的囊泡明显更大(肥大),尽管慢性人类血吸虫病中不存在杯状细胞增生。此外,我们还检查了对照组和血吸虫感染患者的大肠上皮中的微绒毛细胞。在小鼠的寄生虫感染过程中,微绒毛细胞的数量会增加,但这些细胞在人类寄生虫感染中尚未被描述。我们在人类血吸虫感染期间没有发现微绒毛细胞增生的证据。因此,我们的研究为人类肠道上皮中与血吸虫相关的变化提供了新的见解,表明大肠杯状细胞的黏液产生增加,但对微绒毛细胞数量的影响相对较小。