The FlowCellect™ GPCR identification kits are designed for flow cytometry applications, which can be used for the identification and quantification of the surface expression level of GPCRs on any cells. The kit uses a GPCR antibody validated for flow cytometry to detect receptor expression, and also includes both positive and negative control cells with well characterized receptor expression levels for the purpose of quantification.
Chemokine receptors are very attractive targets because they are highly expressed on immune cells and regulate leukocyte activation and trafficking. Many of these targets have been indicated to play a key role in certain diseases states such as HIV infection, Rheumatoid Arthritis, and Diabetes. The expression levels of these receptors often reflect the different states of infectious diseases and inflammation.
Chemokine receptors are seven transmembrane G-Protein coupled receptors (GPCRs). The chemokine receptor family comprises of eighteen GPCR targets, in which ten are CC chemokine receptors, seven are CXC chemokine receptors, and one is a CX3C chemokine receptor. Currently, Millipore has launched 12 GPCR surface identification kits with an initial focus on the chemokine receptor family.
The chemokine SDF-1 and its GPCR receptor CXCR4 have a one-to-one specificity that is unique among chemokines and their receptors. SDF-1 binds to CXCR4 expressed on hematopoietic and lymphopoietic cells, and directs their trafficking to and retention in hemato-and lymphatopoietic organs and sites of inflammation [3]. CXCR4 is expressed on several tumor cell lineages and might be responsible for metastasis to sites of SDF-1 expression, such as bone and lymph nodes [4]. In addition, CXCR4 is a co-receptor for the HIV envelope glycoprotein gp120 [2]. Small molecule antagonists of CXCR4 have been developed and shown to inhibit infectivity of T-tropic HIV strains and to impair growth of brain tumors [1,7].
The control cells provided in the kit are based on the commercially available ChemiScreen™ GPCR stable cell lines from Millipore. Both the positive and negative control cell lines have been fully characterized using Pharmacology techniques such as radioligand binding assay to determine the receptor number for each cell type [6]. Using this information, now the researcher can determine the number of receptors per cell on any given cell type.