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Guanylate-binding proteins (GBPs) are a group interferon-inducible GTPases within the constellation of the dynamin GTPase superfamily. These proteins restrict the replication of intracellular pathogens in both immune and non-immune cells. GBPs and their related family members immunity-related GTPases target and lyse the membrane of the pathogen-containing vacuole, destroying the residential niche of vacuolar protozoal and bacterial pathogens. They also prevent virion infectivity and target replication complexes of ribonucleic acid viruses. The exciting concept that GBPs and immunity-related GTPases can directly target the membrane of bacteria and protozoa has emerged. Rupture and lysis of the pathogen membrane mediates liberation of concealed microbial ligands for activation of innate immune sensing pathways and the inflammasome. Further studies have demonstrated a capacity of GBPs to recruit additional antimicrobial factors, highlighting the complexity of the molecular mechanisms involved in pathogen killing. In this mini-review, we discuss recent advances describing the localisation and functions of GBPs on the host and pathogen membrane. We also highlight unresolved questions related to the regulation of GBPs in cell-autonomous immunity to intracellular pathogens.
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http://dx.doi.org/10.1111/cmi.12791 | DOI Listing |
New Phytol
August 2025
INRAE, Université de Bordeaux, UMR1332 Biologie du Fruit et Pathologie, Villenave d'Ornon, F-33140, France.
Guanylate-binding proteins (GBPs) are large GTPases that belong to the Dynamin Superfamily Protein family. In humans, GBPs are well-characterized interferon-induced GTPases, playing a central role in cell-autonomous innate immunity against infections, inflammation and cancer. GBPs orthologs have been identified in plants only recently.
View Article and Find Full Text PDFClin Chim Acta
August 2025
Laboratory Medicine, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou 510000, PR China; School of Medical Technology, Xuzhou Key Laboratory of Laboratory Diagnostics, Xuzhou Medical University, Xuzhou 221004 Jiangsu, PR China. Ele
Background: Early differentiation between Mycobacterium tuberculosis (MTB) and non-tuberculous mycobacteria (NTM) is critical due to distinct treatment protocols. Traditional diagnostic methods, including acid-fast staining, bacterial culture, and nucleic acid assays, often face challenges. This study evaluated the diagnostic value of Guanylate-Binding Protein 1 (GBP1), interferon-gamma (IFN-γ), and interleukin-2 (IL-2) in peripheral blood for distinguishing active TB, NTM infections, and cured TB.
View Article and Find Full Text PDFBlood Neoplasia
August 2025
Department of Medicine, Division of Oncology, Washington University School of Medicine, St. Louis, MO.
Mutations in the histone methyltransferase enhancer of zeste homolog 2 (EZH2), particularly the neomorphic Y641F hot spot mutation, are implicated in hematologic malignancies. However, how developmental timing and cellular context influence their oncogenic potential remains poorly understood. Here, we used a conditional allele with multiple tissue-specific Cre drivers to investigate the effects of these mutations across hematopoietic development.
View Article and Find Full Text PDFInfect Immun
September 2025
Department of Clinical Laboratory, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
The guanylate-binding protein (GBP) family, a group of interferon-induced GTPases, is pivotal in pathogen defense, inflammation regulation, and tumor immunity. Among them, GBP5 has emerged as a key player due to its distinctive roles in various diseases. However, existing studies reveal significant gaps, particularly regarding its expression, regulatory mechanisms, and functional dynamics across diverse diseases and patient populations, limiting its reliability as a biomarker or therapeutic target.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
August 2025
Department of Biomedical Sciences, School of Life Sciences, Tokyo University of Pharmacy and Life Sciences, Hachioji, Tokyo 192-0392, Japan.
The interferon (IFN)-inducible GTPases play a crucial role in cell autonomous immunity against intracellular pathogens. Particularly, these GTPases directly recognize the host membrane-derived vacuole containing pathogens and subsequently destroy it. Although it has been revealed that these GTPases target the membrane of ()-containing vacuole (LCV), molecular mechanism has been totally uncleared.
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