Lymphocyte antigen 96

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Toll-like receptor pathways revised

Lymphocyte antigen 96 (LY96), also known as MD-2, is a protein that in humans is encoded by the LY96 gene. LY96 is a key component in the immune system, playing a crucial role in the body's defense mechanism against pathogens. It is closely associated with Toll-like receptor 4 (TLR4) and is essential for the recognition and signal transduction of lipopolysaccharides (LPS), molecules found on the outer membrane of Gram-negative bacteria.

Function[edit | edit source]

LY96 is a membrane protein that, together with TLR4, forms a complex that can recognize and bind to lipopolysaccharides. This binding is a critical step in the innate immune response, leading to the activation of nuclear factor kappa B (NF-κB) and the production of pro-inflammatory cytokines. These cytokines play a significant role in the immune system's response to infection by promoting inflammation and recruiting other immune cells to the site of infection.

Structure[edit | edit source]

The LY96 protein is small, consisting of approximately 160 amino acids. It has a unique structure that allows it to bind tightly to TLR4, facilitating the recognition of LPS. The LY96-TLR4 complex is located on the surface of immune cells, such as macrophages and dendritic cells, which are among the first cells to respond to bacterial invasion.

Clinical Significance[edit | edit source]

Alterations in the expression or function of LY96 can lead to abnormal immune responses. For example, overactivation of the LY96-TLR4 pathway can result in excessive inflammation, contributing to the pathogenesis of various inflammatory and autoimmune diseases. Conversely, a deficiency in LY96 function can impair the body's ability to detect and respond to bacterial infections, leading to increased susceptibility to these infections.

Research into LY96 has also highlighted its potential role in the development of new therapeutic strategies for treating inflammatory diseases and sepsis. By targeting the LY96-TLR4 signaling pathway, it may be possible to modulate the immune response, reducing harmful inflammation while still fighting off infection.

See Also[edit | edit source]

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Contributors: Prab R. Tumpati, MD