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CXCL9
Mammalian protein found in Homo sapiens From Wikipedia, the free encyclopedia
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Chemokine (C-X-C motif) ligand 9 (CXCL9) is a small cytokine belonging to the CXC chemokine family that is also known as monokine induced by gamma interferon (MIG). The CXCL9 is one of the chemokine which plays role to induce chemotaxis, promote differentiation and multiplication of leukocytes, and cause tissue extravasation.[5]
It is closely related to two other CXC chemokines called CXCL10 and CXCL11, whose genes are located near the gene for CXCL9 on human chromosome 4.[6][7] CXCL9, CXCL10 and CXCL11 all elicit their chemotactic functions by interacting with the chemokine receptor CXCR3.[8]
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Structre
Chemokine (C-X-C motif) ligand 9 (CXCL9) exhibits the classic structure of CXC chemokines, characterized by a short and flexible N-terminal region, a well-ordered core stabilized by two disulfide bonds, three antiparallel beta-strands, and a C-terminal alpha-helix.[9] This conserved tertiary structure provides both stability and the necessary conformational flexibility at the N- and C-termini, enabling effective interactions with its receptor, CXCR3, and facilitating signal transduction essential for immune cell migration and activation.[9] The structural core is highly conserved among CXC chemokines, while variations in the loop regions contribute to differences in receptor binding and functional specificity.[9]
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Function
Summarize
Perspective
The CXCL9/CXCR3 receptor regulates immune cell migration, differentiation, and activation. Immune reactivity occurs through recruitment of immune cells, such as cytotoxic lymphocytes (CTLs), natural killer (NK) cells, NKT cells, and macrophages. Th1 polarization also activates the immune cells in response to IFN-γ.[10] Tumor-infiltrating lymphocytes are a key for clinical outcomes and prediction of the response to checkpoint inhibitors.[11] In vivo studies suggest the axis plays a tumorigenic role by increasing tumor proliferation and metastasis.[citation needed] CXCL9 predominantly mediates lymphocytic infiltration to the focal sites and suppresses tumor growth.[12]
Immune modulation
In immune cell differentiation, several reports indicate that CXCL9 promotes T helper 1 (Th1) polarization through CXCR3.[13] An in vivo model by Zohar et al. demonstrated that CXCL9 increased the transcription of T-bet and RORγ, leading to the polarization of Foxp3− type 1 regulatory (Tr1) cells or Th17 cells from naïve T cells via STAT1, STAT4, and STAT5 phosphorylation.[13]
Several studies have shown that tumor-associated macrophages (TAMs) exert modulatory effects in the tumor microenvironment (TME), with the CXCL9/CXCR3 axis influencing TAM polarization. TAMs can exhibit opposing effects: M1 macrophages promote anti-tumor activity, while M2 macrophages support tumor progression. Oghumu et al. found that mice deficient in CXCR3 displayed increased IL-4 production and M2 polarization in a murine breast cancer model, accompanied by reduced innate and immune cell-mediated anti-tumor responses.[14]
Regarding immune cell activation, CXCL9 stimulates Th1 polarization and activation, leading to the production of IFN-γ, TNF-α, and IL-2. This enhances anti-tumor immunity by activating cytotoxic T lymphocytes (CTLs), NK cells, and macrophages.[15] Additionally, the IFN-γ-dependent immune activation loop further promotes CXCL9 release.[5] Immune cells such as Th1 cells, CTLs, NK cells, and NKT cells exert anti-tumor effects against cancer cells via paracrine CXCL9/CXCR3 signaling in tumor models.[12] In contrast, autocrine CXCL9/CXCR3 signaling in cancer cells has been implicated in promoting cancer cell proliferation, angiogenesis, and metastasis.[citation needed]
Immune checkpoint regulation
The relationship between the CXCL9/CXCR3 axis and the PD-L1/PD-1 pathway is important in immune regulation. Programmed cell death protein 1 (PD-1) expression is increased on T cells within the tumor site compared to T cells in peripheral blood. Anti-PD-1 therapy can inhibit "immune escape" and enhance immune activation.[16] Peng et al. demonstrated that anti-PD-1 therapy not only enhanced T cell-mediated tumor regression but also increased the expression of IFN-γ, though not CXCL9, in bone marrow-derived cells.[16] Blockade of the PD-L1/PD-1 axis in T cells may induce a positive feedback loop at the tumor site through the CXCL9/CXCR3 axis. Additionally, treatment with an anti-CTLA4 antibody led to a significant upregulation of this axis in pretreatment melanoma lesions from patients who exhibited a favorable clinical response to ipilimumab.[17]
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Clinical signficance
Biomarkers
CXCL9, -10, -11 have proven to be valid biomarkers for the development of heart failure and left ventricular dysfunction, suggesting an underlining pathophysiological relation between levels of these chemokines and the development of adverse cardiac remodeling.[18][19]
This chemokine has also been associated as a biomarker for diagnosing Q fever infections.[20]
Melanoma
CXCL9 has also been identified as candidate biomarker of adoptive T cell transfer therapy in metastatic melanoma.[21] The role of CXCL9/CXCR3 in TME and immune response - this plays a critical role in immune activation through paracrine signaling, impacting efficacy of cancer treatments.[5]
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External links
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