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人 PILRA 抗体对
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人 PILRA 抗体对

01AB03428

Paired immunoglobin like type 2 receptor alpha (PILRA) is a type I transmembrane glycoprotein primarily expressed on myeloid cells, including microglia and macrophages. It functions as an inhibitory receptor that negatively regulates inflammatory responses through its intracellular immunoreceptor tyrosine-based inhibitory motif. PILRA recognizes and binds O-glycosylated ligands, such as complement component 4A and herpes simplex virus-1 glycoprotein B, via a sialic acid-binding pocket in its extracellular Ig-like domain. This interaction is crucial for modulating innate immune signaling and maintaining immune homeostasis. Clinically, the G78R genetic variant of PILRA is well-established as a protective factor against Alzheimer's disease, as it reduces ligand affinity and limits microglial inhibition. Additionally, PILRA serves as an entry receptor for HSV-1, and its dysregulation is linked to altered susceptibility to viral infections and inflammatory conditions, emphasizing its role as a key checkpoint in myeloid cell activation.

Human
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技术参数

靶点基因名
PILRA
蛋白别名
paired immunoglobin like type 2 receptor alpha; PILRA
UniProt
Q9UKJ1
物种
Human

产品详情

靶点名称
PILRA
蛋白名称
paired immunoglobin like type 2 receptor alpha
蛋白别名
Paired immunoglobulin-like type 2 receptor alpha; Cell surface receptor FDF03; Inhibitory receptor PILR-alpha
靶点基因名
PILRA
UniProt
Q9UKJ1
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

Paired immunoglobin like type 2 receptor alpha (PILRA) is a type I transmembrane glycoprotein primarily expressed on myeloid cells, including microglia and macrophages. It functions as an inhibitory receptor that negatively regulates inflammatory responses through its intracellular immunoreceptor tyrosine-based inhibitory motif. PILRA recognizes and binds O-glycosylated ligands, such as complement component 4A and herpes simplex virus-1 glycoprotein B, via a sialic acid-binding pocket in its extracellular Ig-like domain. This interaction is crucial for modulating innate immune signaling and maintaining immune homeostasis. Clinically, the G78R genetic variant of PILRA is well-established as a protective factor against Alzheimer's disease, as it reduces ligand affinity and limits microglial inhibition. Additionally, PILRA serves as an entry receptor for HSV-1, and its dysregulation is linked to altered susceptibility to viral infections and inflammatory conditions, emphasizing its role as a key checkpoint in myeloid cell activation.