Exosome‐derived long noncoding RNAs: Mediators of host–Plasmodium parasite communication

Author:

Chen Jin‐guang1ORCID,Liu Shuang‐chun2,Nie Qing3,Du Yun‐ting4,Lv Yin‐yi1,He Lian‐ping1ORCID,Chen Guang1ORCID

Affiliation:

1. Taizhou Central Hospital (Taizhou University Hospital), Taizhou University Taizhou China

2. Municipal Hospital Affiliated to Medical School of Taizhou University Taizhou China

3. Weifang Centers for Disease Control and Prevention Weifang Shandong Province China

4. Department of Laboratory Medicine Cancer Hospital of China Medical University, Liaoning Cancer Hospital & Institute Shenyang China

Abstract

AbstractOvercoming challenges associated with malaria eradication proves to be a formidable task due to the complicated life cycle exhibited by the malaria parasite and the lack of safe and enduring vaccines against malaria. Investigating the interplay between Plasmodium parasites and their mammalian hosts is crucial for the development of novel vaccines. Long noncoding RNAs (lncRNAs) derived from Plasmodium parasites or host cells have emerged as potential signaling molecules involved in the trafficking of proteins, RNA (mRNAs, miRNAs, and ncRNAs), and DNA. These lncRNAs facilitate the interaction between hosts and parasites, impacting normal physiology or pathology in malaria‐infected individuals. Moreover, they possess the capacity to regulate immune responses and associated signaling pathways, thus potentially influencing chromatin organization, epigenetic modifications, mRNA processing, splicing, and translation. However, the functional role of exosomal lncRNAs in malaria remains poorly understood. This review offers a comprehensive analysis of lncRNA and exosomal lncRNA profiles during malaria infection. It presents an overview of recent progress in elucidating the involvement of exosomal lncRNAs in host–parasite interactions. Additionally, potential exosomal lncRNAs linked to the domains of innate and adaptive immunity in the context of malaria are proposed. These findings may contribute to the discovery of new diagnostic and therapeutic strategies for malaria. Furthermore, the need for additional research was highlighted that aimed to elucidate the mechanisms underlying lncRNA transportation into host cells and their targeting of specific genes to regulate the host's immune response. This knowledge gap presents an opportunity for future investigations, offering innovative approaches to enhance malarial control.This article is categorized under: RNA Interactions with Proteins and Other Molecules > Small Molecule‐RNA Interactions RNA Interactions with Proteins and Other Molecules > Protein‐RNA Interactions: Functional Implications RNA in Disease and Development > RNA in Disease

Funder

National Natural Science Foundation of China

Natural Science Foundation of Zhejiang Province

Taizhou Municipal Science and Technology Bureau

Publisher

Wiley

Subject

Molecular Biology,Biochemistry

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