Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Gewählte Publikation:
SHR Neuro Krebs Kardio Lipid Stoffw Microb
Zhang, H; Zhu, X; Friesen, TJ; Kwak, JW; Pisarenko, T; Mekvanich, S; Velasco, MA; Randolph, TW; Kargl, J; Houghton, AM.
Annexin A2/TLR2/MYD88 pathway induces arginase 1 expression in tumor-associated neutrophils.
J Clin Invest. 2022; 132(22):
Doi: 10.1172/JCI153643
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- Kargl Julia
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- Abstract:
- Myeloid lineage cells suppress T cell viability through arginine depletion via arginase 1 (ARG1). Despite numerous studies exploring the mechanisms by which ARG1 perturbs lymphocyte function, the cellular populations responsible for its generation and release remain poorly understood. Here, we showed that neutrophil lineage cells and not monocytes or macrophages expressed ARG1 in human non-small cell lung cancer (NSCLC). Importantly, we showed that approximately 40% of tumor-associated neutrophils (TANs) actively transcribed ARG1 mRNA. To determine the mechanism by which ARG1 mRNA is induced in TANs, we utilized FPLC followed by MS/MS to screen tumor-derived factors capable of inducing ARG1 mRNA expression in neutrophils. These studies identified ANXA2 as the major driver of ARG1 mRNA expression in TANs. Mechanistically, ANXA2 signaled through the TLR2/MYD88 axis in neutrophils to induce ARG1 mRNA expression. The current study describes what we believe to be a novel mechanism by which ARG1 mRNA expression is regulated in neutrophils in cancer and highlights the central role that neutrophil lineage cells play in the suppression of tumor-infiltrating lymphocytes.
- Find related publications in this database (using NLM MeSH Indexing)
- Humans - administration & dosage
- Annexin A2 - genetics
- Arginase - metabolism
- Carcinoma, Non-Small-Cell Lung - genetics
- Lung Neoplasms - genetics
- Myeloid Differentiation Factor 88 - genetics, metabolism
- Neutrophils - metabolism
- RNA, Messenger - administration & dosage
- Tandem Mass Spectrometry - administration & dosage
- Toll-Like Receptor 2 - genetics, metabolism