Neuroinflammation related Antibody Products

Neuroinflammation related Antibody Products


Background

The central nervous system (CNS) initiates a range of responses to maintain homeostasis in both pathological and physiological states. This collection of responses, collectively termed "neuroinflammation," involves the coordinated actions of various cellular and molecular processes aimed at detecting potential threats, mitigating their effects, and repairing resultant damage. Amerigo Scientific offers a selection of internally developed and validated antibodies related to neuroinflammation, tailored to meet your specific research needs.

Overview of Neuroinflammation

Neuroinflammation refers to the inflammation of nervous tissue and can be triggered by various factors, including traumatic brain injury, toxic metabolites, infections, or autoimmune reactions, which disrupt the homeostasis of the central nervous system (CNS). The CNS is usually an immunologically privileged site, shielded by the blood-brain barrier (BBB) from peripheral immune cells. However, when the BBB is compromised, an amplified immune response originally aims to protect the CNS from pathogens, but results in extensive toxicity and widespread inflammation, further facilitating leukocyte migration through the BBB. Neuroinflammation involves numerous signaling pathways, receptors, and various cell types.

Fig.1 The initiation of neuroinflammation.Fig.1 The onset of neuroinflammation within the organism.Distributed under CC BY-SA 4.0, from Wiki, without modification.

Mechanisms of Neuroinflammation

Monocytes and clonotypic immune cells are pivotal in neuroinflammation, serving as physiological protectors against pathogens and particularly neurotropic viruses. These cells also play crucial roles in maintaining CNS structure and function, influencing development, and enhancing cognitive abilities. In neurodegenerative diseases, however, these immune cells become dysregulated, affecting both their levels and functions, leading to aberrant immune responses. This dysregulation often results in altered monocyte profiles and phenotypes, both peripherally and centrally, impacting their quantity and quality.

Fig.2 Important drivers of neuroinflammation.Fig.2 Recent insights on peripheral and infiltrating monocytes and clonotypic immune cells in neuroinflammation.1

Functions of Neuroinflammation

While neuroinflammation is often viewed negatively due to its association with pathology, it encompasses a spectrum of responses, some beneficial. In CNS injuries, a balance between inflammation and repair processes can aid functional recovery. The intensity and duration of inflammation determine whether immune signals support or harm the CNS. Beneficial responses include immune-to-brain signaling post-infection, which reorganizes host priorities, and interleukins like IL-1 and IL-4, which aid learning, memory, and recovery post-injury. Conversely, maladaptive responses involve chronic inflammation marked by cytokines (IL-1, TNF), reactive oxygen species, and peripheral immune cell recruitment, leading to neurodegeneration and cognitive decline.

Key Targets of Neuroinflammation Research

CCL2 CD200 CXCR1 IL10RA IL1RAP CXCL8 TLR4
CCL21 IL17A CXCR2 IL10RB IL2 ITGAM TLR5
CCL3 PTGS2 CXCR3 IL18 IL23A LTA TLR6
CCL5 CX3CL1 CXCR4 IL18R1 IL23R NFE2L2 TLR7
CCL14 CXCL1 GFAP IL1A IL2RA PTGES2 TLR8
CCR2 CXCL10 ICAM1 IL1B IL2RB TLR1 TLR9
CCR5 CXCL12 IFNG IL1R1 IL6 TLR2 TNF
CD2 CXCL2 IL10 IL1R2 IL6R TLR3 TNFRSF1A

Amerigo Scientific offers a comprehensive selection of recombinant antibodies across various species, isotypes, and configurations. If you are unable to locate the specific antibody required, our custom antibody engineering services are prepared to meet your needs. Browse our collection of antibodies related to neuroinflammation, or contact us for inquiries or quotes. We are keen to assist you.

Reference

  1. Balistreri, Carmela Rita, and Roberto Monastero. "Neuroinflammation and Neurodegenerative Diseases: How Much Do We Still Not Know?" Brain Sciences 14.1 (2023): 19. Distributed under Open Access license CC BY 4.0, without modification.

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