Complement meets Tau: Exploring the effects of a novel C3‐targeting siRNA in a Tauopathy mouse model
Abstract Background Complement C3 is a potential therapeutic target in AD. Tau P301S (PS19) mice have emerged as a powerful tool in studying tau pathology. Complement C3aR has been shown to be critical in mediating immune homeostasis and tau pathology in this model, while C3 deficiency mitigated neurodegeneration and neuronal loss.
Maria‐Tzousi Papavergi +5 more
wiley +1 more source
The role of the complement system in traumatic brain injury: a review [PDF]
Traumatic brain injury (TBI) is an important cause of disability and mortality in the western world. While the initial injury sustained results in damage, it is the subsequent secondary cascade that is thought to be the significant determinant of ...
A Alawieh +124 more
core +1 more source
Cellular Communication Networks Mediated by Microglia in Ischemic Stroke
After ischemic stroke, microglia serve as central regulators within the neuroimmune network, engaging in dynamic crosstalk with neurons, astrocytes, vascular endothelial cells, and peripheral immune cells. By releasing cytokines, chemokines, extracellular vesicles, and transmitting mechanical signals, activated microglia coordinate inflammatory ...
Feiyu Ma +5 more
wiley +1 more source
Isomer Dependence in the Assembly and Lability of Silver(I) Trifluoromethanesulfonate Complexes of the Heteroditopic Ligands, 2-, 3-, and 4-[Di(1\u3cem\u3eH\u3c/em\u3e-pyrazolyl)methyl]phenyl(di-\u3cem\u3ep\u3c/em\u3e-tolyl)phosphine [PDF]
Three isomers of a new heteroditopic ligand that contains a di(1H-pyrazolyl)methyl (−CHpz2) moiety connected to a di(p-tolyl)phosphine group via a para-, meta-, or ortho-phenylene spacer (pL, mL, and oL, respectively) have been synthesized by using a ...
Gardinier, James R. +2 more
core +1 more source
HLDA Workshops were established 40 years ago to develop a standardized CD molecule nomenclature for leukocyte cell‐surface molecules by comparing monoclonal antibodies (mAbs) produced by different laboratories and companies. The HLDA11 Workshop focused on validating G‐protein‐coupled receptors (GPCRs) targeting mAbs and assessing cell‐type‐specific ...
Javier Fernández‐Calles +9 more
wiley +1 more source
Objective To investigate the effect of astrocyte-microglia crosstalk mediated by complement C3/C3aR signaling on hydrocephalus after germinal matrix hemorrhage (GMH) in newborn rats.
GENG Junjun +4 more
doaj +1 more source
Molecular mechanisms of inflammation and tissue injury after major trauma-is complement the "bad guy"? [PDF]
Trauma represents the leading cause of death among young people in industrialized countries. Recent clinical and experimental studies have brought increasing evidence for activation of the innate immune system in contributing to the pathogenesis of ...
Miriam D Neher +4 more
core +2 more sources
The C3-C3aR axis modulates trained immunity in alveolar macrophages
Abstract Complement protein C3 is crucial for immune responses in mucosal sites such as the lung, where it aids in microbe elimination and enhances inflammation. While trained immunity – enhanced secondary responses of innate immune cells after prior exposure – is well-studied, the role of the complement system in trained immune ...
Alexander P. Earhart +9 more
openaire +3 more sources
Cancer immunotherapy has made remarkable clinical advances in recent years. Antibodies targeting the immune checkpoint receptors PD-1 and CTLA-4 and adoptive cell therapy (ACT) based on ex vivo expanded peripheral CTLs, tumor infiltrating lymphocytes ...
Yu Wang, Hui Zhang, You-Wen He
doaj +1 more source
Calcareous nannofossil biostratigraphy of the M. del Casino section (northern Apennines, Italy) and paleoceanographic conditions at times of Late Miocene sapropel formation [PDF]
A detailed quantitative calcareous nannofossil analysis has been performed on 138 samples from the astronomically dated Monte del Casino section with the aim to identify and precisely date the most important calcareous nannofossil events across the ...
Giunta, S. +4 more
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