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Pattern Recognition Receptors: Innate Immunity and Beyond

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Immunology".

Deadline for manuscript submissions: closed (31 July 2021) | Viewed by 3430

Special Issue Editors


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Guest Editor
Department of Life Sciences, Brunel University London, Uxbridge, UK
Interests: innate immunity; nanomedicine; drug targeting; allergy; cancer; pregnancy; infection
Special Issues, Collections and Topics in MDPI journals

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Guest Editor
Department of Zoology, Cooch Behar Panchanan Barma University, West Bengal, India
Interests: innate immunity; cancer; pregnancy; hypersensitivity; immunotherapy with natural compounds

Special Issue Information

Dear Colleagues,

The initiation of the first line defense mechanism of the immune system, the innate immune defense, relies on the capacity of recognition molecules to recognize a variety of numerous invading microorganisms. These pattern recognition receptors (PRRs) include cellular pattern recognition receptors and extracellular soluble PRRs and can bind to highly conserved structures on microorganisms and altered self, termed as pathogen-associated molecular patterns (PAMPs) and damage-associated molecular patterns (DAMPs), respectively. PRRs are either present on many effector cells of the immune system and in non-immune cells, or are rapidly secreted in the serum by a variety of cells and tissues in response to pathogen invasion. The cellular PRRs, such as Toll-like receptors (TLRs), NOD-like receptors and RIG-I like receptors as well as soluble PRRs, such as collectins, ficolins, pentraxins, natural IgM antibodies and complement recognition subcomponents, play a crucial role in pathogen recognition. Upon PRRs recognition of evading microorganisms, immune responses are initiated that lead to elimination of pathogens through shared common mechanisms, such as the activation of the complement system, opsonization, neutralization and regulation of inflammation. Due to their high importance in immune defense, dysfunction or abnormal expression of PRRs may play an important role in the pathogenesis of human diseases. Although defined as the major players of the innate immune system, PRRs also profoundly influence the activation and regulation of the adaptive immunity. There are key events, such as PRR signalling, translocation of cytosolic PRRs to cell compartments, negative regulation of PRR and host chromatin remodelling, that connect the innate immune surveillance with subsequent adaptive immune response to infection and stress. Some PRRs have functions beyond their participation in the immune system. It is not surprising that their importance has been recognized in autoimmunity, pregnancy, reproduction, cancer, transplantation, vaccination.

For this Special Issue we invite researchers to contribute original research manuscripts and review articles that address the diverse functions of cellular and soluble PRRs in the normal physiology and disease conditions.

Prof. Dr. Uday Kishore
Dr. Hadida Yasmin
Guest Editors

Manuscript Submission Information

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Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. International Journal of Molecular Sciences is an international peer-reviewed open access semimonthly journal published by MDPI.

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Keywords

  • Innate immunity
  • Adaptive immunity
  • Pattern recognition receptors
  • Host–pathogen interaction
  • Autoimmune diseases
  • Pregnancy
  • Disease mechanisms
  • Complement

Published Papers (1 paper)

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Research

18 pages, 4814 KiB  
Article
Molecular Basis of Complement C1q Collagen-Like Region Interaction with the Immunoglobulin-Like Receptor LAIR-1
by Guillaume Fouët, Isabelle Bally, Anne Chouquet, Jean-Baptiste Reiser, Nicole M. Thielens, Christine Gaboriaud and Véronique Rossi
Int. J. Mol. Sci. 2021, 22(10), 5125; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms22105125 - 12 May 2021
Cited by 10 | Viewed by 2821
Abstract
The immune system homeostasis relies on a tight equilibrium of interconnected stimulatory and inhibitory signals. Disruption of this balance is characteristic of autoimmune diseases such as systemic lupus erythematosus (SLE). Aside from activating the classical complement pathway and enhancing pathogens and apoptotic cells [...] Read more.
The immune system homeostasis relies on a tight equilibrium of interconnected stimulatory and inhibitory signals. Disruption of this balance is characteristic of autoimmune diseases such as systemic lupus erythematosus (SLE). Aside from activating the classical complement pathway and enhancing pathogens and apoptotic cells phagocytosis, C1q has been recently shown to play an important role in immune modulation and tolerance by interacting with several inhibitory and stimulatory immune receptors. Due to its functional organization into collagen-like (CLR) and globular (GR) regions and its multimeric nature, C1q is able to interact simultaneously with several of these receptors and locally congregate pro- and anti-inflammatory signals, thus modulating the immune response. Leukocyte associated immunoglobulin-like (Ig-like) receptor 1 (LAIR-1), a ubiquitous collagen receptor expressed in many immune cell types, has been reported to interact with the CLR of C1q. In this study, we provide new insights into the molecular and structural determinants underlying C1q/LAIR-1 interaction. Recombinant LAIR-1 extracellular Ig-like domain was produced and tested for its interaction with C1q. A molecular dissection of C1q combined with competition assays reveals that LAIR-1 interacts with C1q’s CLR through a binding site close but different from the one of its associated C1r2s2 proteases tetramer. On the other side, we identified LAIR-1 residues involved in C1q interaction by site-directed mutational analysis. All together, these results lead to propose a possible model for C1q interaction with LAIR-1 and will contribute to the fundamental understanding of C1q-mediated immune tolerance. Full article
(This article belongs to the Special Issue Pattern Recognition Receptors: Innate Immunity and Beyond)
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