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Unrevealing the Mystery of Latent Leishmaniasis: What Cells Can Host ?

作者信息

Valigurová Andrea, Kolářová Iva

机构信息

Department of Botany and Zoology, Faculty of Science, Masaryk University, Kotlářská 2, 611 37 Brno, Czech Republic.

Department of Parasitology, Faculty of Science, Charles University, Albertov 6, 128 44 Prague, Czech Republic.

出版信息

Pathogens. 2023 Feb 3;12(2):246. doi: 10.3390/pathogens12020246.


DOI:10.3390/pathogens12020246
PMID:36839518
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9967396/
Abstract

spp. (Kinetoplastida) are unicellular parasites causing leishmaniases, neglected tropical diseases of medical and veterinary importance. In the vertebrate host, parasites multiply intracellularly in professional phagocytes, such as monocytes and macrophages. However, their close relative with intracellular development--can unlock even non-professional phagocytes. Since and have similar organelle equipment, is it possible that can invade and even proliferate in cells other than the professional phagocytes? Additionally, could these cells play a role in the long-term persistence of in the host, even in cured individuals? In this review, we provide (i) an overview of non-canonical host cells and (ii) an insight into the strategies that may use to enter them. Many studies point to fibroblasts as already established host cells that are important in latent leishmaniasis and disease epidemiology, as they support transformation into amastigotes and even their multiplication. To invade them, causes damage to their plasma membrane and exploits the subsequent repair mechanism via lysosome-triggered endocytosis. Unrevealing the interactions between and its non-canonical host cells may shed light on the persistence of these parasites in vertebrate hosts, a way to control latent leishmaniasis.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cf/9967396/ae1ba8e679e1/pathogens-12-00246-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cf/9967396/9d50f146d93a/pathogens-12-00246-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cf/9967396/ae1ba8e679e1/pathogens-12-00246-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cf/9967396/9d50f146d93a/pathogens-12-00246-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84cf/9967396/ae1ba8e679e1/pathogens-12-00246-g002.jpg

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Unrevealing the Mystery of Latent Leishmaniasis: What Cells Can Host ?

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[9]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Superparamagnetic Iron Oxide-Labeled Can Be Traced in Fibroblasts.

J Parasitol Res. 2023-1-4

[2]
Transcriptional Profiling of Infected Dendritic Cells: Insights into the Role of Immunometabolism in Host-Parasite Interaction.

Microorganisms. 2022-6-22

[3]
In vivo transcriptional analysis of mice infected with Leishmania major unveils cellular heterogeneity and altered transcriptomic profiling at single-cell resolution.

PLoS Negl Trop Dis. 2022-7

[4]
Visceral Leishmaniasis and the Skin: Dermal Parasite Transmission to Sand Flies.

Pathogens. 2022-5-24

[5]
Sand flies: Basic information on the vectors of leishmaniasis and their interactions with Leishmania parasites.

Commun Biol. 2022-4-4

[6]
Causative Agents of American Tegumentary Leishmaniasis Are Able to Infect 3T3-L1 Adipocytes .

Front Cell Infect Microbiol. 2022

[7]
Hide-and-Seek: A Game Played between Parasitic Protists and Their Hosts.

Microorganisms. 2021-11-25

[8]
Promastigotes Enhance Neutrophil Recruitment through the Production of CXCL8 by Endothelial Cells.

Pathogens. 2021-10-26

[9]
Identification of adipocytes as target cells for Leishmania infantum parasites.

Sci Rep. 2021-10-28

[10]
The Paradox of a Phagosomal Lifestyle: How Innate Host Cell- Interactions Lead to a Progressive Chronic Disease.

Front Immunol. 2021

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