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Human adenosine deaminase 2 induces differentiation of monocytes into macrophages and stimulates proliferation of T helper cells and macrophages

Authors :
Nicolas Glaichenhaus
Andrey V. Zavialov
Eduard Gracia
Anton V. Zavialov
Grégoire Lauvau
Rafael Franco
Immunologie des maladies infectieuses allergiques et autoimmunes
Université Nice Sophia Antipolis (... - 2019) (UNS)
COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Institut National de la Santé et de la Recherche Médicale (INSERM)
Laboratory of Immune Regulation
Singapore Immunology Network (SIgN)
Centro de Investigacion Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED)
Instituto de Salud Carlos III [Madrid] (ISC)
Department of Molecular Biology
Swedish University of Agricultural Sciences (SLU)
Source :
Biochemical and Biophysical Research Communications, Biochemical and Biophysical Research Communications, Elsevier, 2010, 388 (3), epub ahead of print. ⟨10.1189/jlb.1109764⟩
Publication Year :
2010
Publisher :
HAL CCSD, 2010.

Abstract

Discovery of the growth factor activity of ADA2. ADAs play a pivotal role in regulating the level of adenosine, a signaling molecule controlling a variety of cellular responses by binding to and activating four ADRs. Two enzymes, ADA1 and ADA2, are known to possess ADA activity in humans. Although the structure of ADA1 and its role in lymphocytic activation have been known for a long time, the structure and function of ADA2, a member of ADGF, remain enigmatic. Here, we found that ADA2 is secreted by monocytes undergoing differentiation into macrophages or DCs and that it binds to the cell surface via proteoglycans and ADRs. We demonstrate that ADA1 and ADA2 increase the rate of proliferation of monocyte-activated CD4+ T cells independently of their catalytic activity. We also show that ADA2 induces T cell-dependent differentiation of monocytes into macrophages and stimulates macrophage proliferation. Our discovery of the growth factor-like activity of ADA2 explains clinical observations and suggests that this enzyme could be used as a drug candidate to modulate the immune responses during inflammation and cancer.

Details

Language :
English
ISSN :
0006291X and 10902104
Database :
OpenAIRE
Journal :
Biochemical and Biophysical Research Communications, Biochemical and Biophysical Research Communications, Elsevier, 2010, 388 (3), epub ahead of print. ⟨10.1189/jlb.1109764⟩
Accession number :
edsair.doi.dedup.....6e082c06b6efcda67b0f1664ea542372
Full Text :
https://doi.org/10.1189/jlb.1109764⟩