Innate immunity and neuroinflammation

Copyright © 2013 Abhishek Shastri et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.Inflammation of central nervous system (CNS) is usually associated with trauma and infection. Neuroinflammation occurs in close relation to trauma, infection, and neurodegenerative diseases. Low-level neuroinflammation is considered to have beneficial effects whereas chronic neuroinflammation can be harmful. Innate immune system consisting of pattern-recognition receptors, macrophages, and complement system plays a key role in CNS homeostasis following injury and infection. Here, we discuss how innate immune components can also contribute to neuroinflammation and neurodegeneration

Hemispheric lateralisation and immune function: A systematic review of human research

This is the post-print version of the final paper published in Journal of Neuroimmunology. The published article is available from the link below. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. Copyright @ 2011 Elsevier B.V.Past studies examined relationships between hemispheric lateralisation (HL) and immune system functioning. However, there has been no up-dated systematic review of this research area. This article reviews relevant published studies, evaluates study quality and effect sizes. Eleven studies were selected: three revealing a relationship between weaker left hemisphere function and poorer immune function, three describing a relationship between weaker right hemisphere function and stronger immune functioning, and five describing both relationships. Mean effect-size of the studies was r = 0.536 (range 0.280–0.866). Collectively, studies point at left-HL and stronger immunity relationships. Limitations, mechanisms and clinical implications are discussed

Huntington's disease: An immune perspective

Copyright © 2011 Annapurna Nayaketal. This article has been made available through the Brunel Open Access Publishing Fund.Huntington's disease (HD) is a progressive neurodegenerative disorder that is caused by abnormal expansion of CAG trinucleotide repeats. Neuroinflammation is a typical feature of most neurodegenerative diseases that leads to an array of pathological changes within the affected areas in the brain. The neurodegeneration in HD is also caused by aberrant immune response in the presence of aggregated mutant huntingtin protein. The effects of immune activation in HD nervous system are a relatively unexplored area of research. This paper summarises immunological features associated with development and progression of HD.U. Kishore acknowledges funding via BRIEF and Brunel University’s strategic funding for the Centre of Infection, Immunity and Disease Mechanisms

Omicron: The new variant of concern needs preparedness, not panic

SARS-CoV-2 continues to be a Public Health Emergency of International Concern. On November 26, the World Health Organization (WHO) labeled the omicron type as a covid-19 variant of concern, prompting travel restrictions, a rush to accelerate booster immunization programmes, and new attempts to address vaccination disparities. According to the WHO, omicron is a "very high" concern throughout the world, and preliminary research indicates that it may be a more transmissible type, leading to infection surges (1,2). The Indian government keeps a close eye on the issue and gives appropriate guidelines as needed. Omicron threat will depend on its transmissibility, Virulence, and capacity to evade immunity in those previously vaccinated or infected. Even if the disease is milder, the rapid onslaught of the virus could overwhelm health care systems (doubling time of 2.5 days means 50X increase in 2 weeks) (3). We should ensure mitigation plans are in place to maintain essential health services and that necessary resources are in place to respond to potential surges

Transcriptional factor PU.1 regulates decidual C1q expression in early pregnancy in human

"Copyright: © 2015 Madhukaran, Kishore, Jamil, Teo, Choolani and Lu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms."C1q is the first recognition subcomponent of the complement classical pathway, which in addition to being synthesized in the liver, is also expressed by macrophages and dendritic cells (DCs). Trophoblast invasion during early placentation results in accumulation of debris that triggers the complement system. Hence, both early and late components of the classical pathway are widely distributed in the placenta and decidua. In addition, C1q has recently been shown to significantly contribute to feto-maternal tolerance, trophoblast migration, and spiral artery remodeling, although the exact mechanism remains unknown. Pregnancy in mice, genetically deficient in C1q, mirrors symptoms similar to that of human preeclampsia. Thus, regulated complement activation has been proposed as an essential requirement for normal successful pregnancy. Little is known about the molecular pathways that regulate C1q expression in pregnancy. PU.1, an Ets-family transcription factor, is required for the development of hematopoietic myeloid lineage immune cells, and its expression is tissue-specific. Recently, PU.1 has been shown to regulate C1q gene expression in DCs and macrophages. Here, we have examined if PU.1 transcription factor regulates decidual C1q expression. We used immune-histochemical analysis, PCR, and immunostaining to localize and study the gene expression of PU.1 transcription factor in early human decidua. PU.1 was highly expressed at gene and protein level in early human decidual cells including trophoblast and stromal cells. Surprisingly, nuclear as well as cytoplasmic PU.1 expression was observed. Decidual cells with predominantly nuclear PU.1 expression had higher C1q expression. It is likely that nuclear and cytoplasmic PU.1 localization has a role to play in early pregnancy via regulating C1q expression in the decidua during implantation

Properdin and factor H: Opposing players on the alternative complement pathway "see-saw"

This article has been made available through the Brunel Open Access Publishing Fund.Properdin and factor H are two key regulatory proteins having opposite functions in the alternative complement pathway. Properdin up-regulates the alternative pathway by stabilizing the C3bBb complex, whereas factor H downregulates the pathway by promoting proteolytic degradation of C3b. While factor H is mainly produced in the liver, there are several extrahepatic sources. In addition to the liver, factor H is also synthesized in fetal tubuli, keratinocytes, skin fibroblasts, ocular tissue, adipose tissue, brain, lungs, heart, spleen, pancreas, kidney, muscle, and placenta. Neutrophils are the major source of properdin, and it is also produced by monocytes, T cells and bone marrow progenitor cell line. Properdin is released by neutrophils from intracellular stores following stimulation by N-formyl-methionine-leucine-phenylalanine (fMLP) and tumor necrosis factor alpha (TNF-α). The HEP G2 cells derived from human liver has been found to produce functional properdin. Endothelial cells also produce properdin when induced by shear stress, thus is a physiological source for plasma properdin. The diverse range of extrahepatic sites for synthesis of these two complement regulators suggests the importance and need for local availability of the proteins. Here, we discuss the significance of the local synthesis of properdin and factor H. This assumes greater importance in view of recently identified unexpected and novel roles of properdin and factor H that are potentially independent of their involvement in complement regulation

(R1501) Rotational and Hall Current Effects on a Free Convection MHD Flow with Radiation and Inclined Magnetic Field

Rotational and Hall current effects on a free convection MHD flow with Radiation and inclined magnetic field are studied here. Electrically conducting, viscous, and incompressible fluid is taken. The flow is modelled with the help of partial differential equations. The analytical solutions for the velocity, concentration, and temperature are solved by the Laplace integral transform method. The outcomes acquired have been examined with the help of graphs drawn for different parameters like Hartmann number, Hall current parameter, inclination of magnetic field, angular velocity and radiation parameter, etc. The variation of the Nusselt number has been shown graphically. It is observed that Hall current parameter and inclination of magnetic field reduces the resistive effect of the applied external magnetic field. Such a study assumes importance because both rotation and Hall current induce secondary flow in the flow-field. The conclusion of the study may be useful in the field of solar physics, rotating magnetic stars, rotating MHD induction machine energy generator and many industrial applications

Effect of thermal cycling on the mechanical properties of 350-grade maraging steel

The effects of retained austenite produced by thermal cycling on the mechanical properties of a precipitation-hardened 350-grade commercial maraging steel were examined. The presence of retained austenite caused decreases in the yield strength (YS) and ultimate tensile strength (UTS) and effected a significant increase in the tensile ductility. Increased impact toughness was also produced by this treatment. The mechanical stability of retained austenite was evaluated by tension and impact tests at subambient temperatures. A deformation-induced transformation of the austenite was manifested as load drops on the load-elongation plots at subzero temperatures. This transformation imparts excellent low-temperature ductility to the material. A wide range of strength, ductility, and toughness can be obtained by subjecting the steel to thermal cycling before the precipitation-hardening treatment