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Lipopolysaccharides and Innate Immunity: Potential Usefulness

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

Deadline for manuscript submissions: closed (30 June 2022) | Viewed by 2252

Special Issue Editor


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Guest Editor
Control of Innate Immunity Collaborative Research Association, FROM KAGAWA 3F, Bio laboratory, 2217-16, Hyashi-cho Takamatsu-shi, Kagawa 761-0301, Japan
Interests: LPS; function of tissue macrophages; mode of action of oral administration of LPS; cognitive dysfunction; reverse aging
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Special Issue Information

Dear Colleagues,

Lipopolysaccharide (LPS) has historically been referred to as an endotoxin because its intravascular injection induces dramatic inflammatory responses.

However, with the elucidation of the mechanisms of innate immunity, LPS has come to be regarded as a substance that can regulate innate immune function, and thus, play a preventive role against various diseases, including modern ones. For example, it has been demonstrated that LPS exposure is helpful for the prevention of allergic asthma among children; LPS exerts its effects on the mucosal tissues of the oral cavity, intestinal tract, and skin; while antibiotic-induced impairment of innate immune function can be prevented, or immune function may be restored by LPS intake. These factors suggest that a paradigm shift is underway to re-examine the physiological role of LPS.

In this Special Issue, we will focus on the role of LPS as a regulator of innate immune functioning and have introduced basic and applied approaches, with special attention to the potential usefulness of LPS.

The regulation of innate immune functioning will be a crucial issue in the future for the prevention and treatment of various diseases, including the prevention of COVID-19. In this context, it is timely to highlight the powerful innate immune regulatory effects of LPS as a means of maintaining good health.

Dr. Gen-Ichiro Soma
Guest Editor

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Keywords

  • oral administration of LPS
  • physiological role of LPS
  • TLR-4
  • mechanism(s) of LPS in control of innate immunity
  • structure and functional relationship of LPS

Published Papers (1 paper)

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Research

14 pages, 3442 KiB  
Article
Amniotic LPS-Induced Apoptosis in the Fetal Brain Is Suppressed by Vaginal LPS Preconditioning but Is Promoted by Continuous Ischemic Reperfusion
by Yupeng Dong, Yoshitaka Kimura and Nobuo Yaegashi
Int. J. Mol. Sci. 2022, 23(3), 1787; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms23031787 - 04 Feb 2022
Cited by 2 | Viewed by 1688
Abstract
Chorioamnionitis (CAM) is an increasingly common disease affecting pregnant women which derives from bacterial vaginosis. In different clinical cases, it has been shown that CAM can cause multiple risk factors for fetal brain damage, such as infection, and intra-uterine asphyxia. However, the molecular [...] Read more.
Chorioamnionitis (CAM) is an increasingly common disease affecting pregnant women which derives from bacterial vaginosis. In different clinical cases, it has been shown that CAM can cause multiple risk factors for fetal brain damage, such as infection, and intra-uterine asphyxia. However, the molecular mechanism remains unknown. In this study, we established a novel CAM mouse model by exposing pregnant mice to a combination of three risk factors: vaginal lipopolysaccharides (LPS), amniotic LPS, and ischemic reperfusion. We found amniotic LPS caused Parkinson’s disease-like fetal brain damage, in a dose and time-dependent manner. Moreover, the mechanism of this fetal brain damage is apoptosis induced by amniotic LPS but it was inhibited by being pretreated with a vaginal LPS challenge before amniotic LPS injection. In contrast, amniotic LPS with continuous ischemic reperfusion caused a higher level of apoptotic cell death than amniotic LPS alone. In particular, a potential neuroprotective biomarker phosphorylation (p)-CREB (ser133) appeared in only vaginal LPS preconditioned before amniotic LPS, whereas ischemic reperfusion triggered IKK phosphorylation after amniotic LPS. Despite the need for many future investigations, this study also discussed a developed understanding of the molecular mechanism of how these phenotypes occurred. Full article
(This article belongs to the Special Issue Lipopolysaccharides and Innate Immunity: Potential Usefulness)
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