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Updated: Dec 6, 2025

Murine Model of CD40-activation of B cells
Published on: March 5, 2010
Implications of CD39 in immune-related diseases
Jianrui Zeng1, Zhaochen Ning1, Yuzhong Wang2
1Institute of Immunology and Molecular Medicine, Jining Medical University, Shandong 272067, China.
Abstract:
Extracellular adenosine triphosphate (eATP) mediates pro-inflammatory responses by recruiting and activating inflammatory cells. CD39 can hydrolyze eATP into adenosine monophosphate (AMP), while CD73 can convert AMP into the immunosuppressive nucleoside adenosine (ADO). CD39 is a rate-limiting enzyme in this cascade, which is regarded as an immunological switch shifting the ATP-mediated pro-inflammatory environment to the ADO- mediated anti-inflammatory status. The CD39 expression can be detected in a wide spectrum of immunocytes, which is under the influence of environmental and genetic factors. It is increasingly suggested that, CD39 participates in some pathophysiological processes, like inflammatory bowel disease (IBD), sepsis, multiple sclerosis (MS), allergic diseases, ischemia-reperfusion (I/R) injury, systemic lupus erythematosus (SLE), diabetes and cancer. Here, we focus on the current understanding of CD39 in immunity, and comprehensively illustrate the diverse CD39 functions within a variety of disorders.
Insights
CD39 is an enzyme that acts as an immunological switch, converting pro-inflammatory extracellular ATP into anti-inflammatory adenosine. This review details CD39
Area of Science:
- Immunology
- Biochemistry
- Molecular Biology
Background:
- Extracellular adenosine triphosphate (eATP) promotes inflammation by recruiting immune cells.
- CD39 and CD73 enzymes sequentially metabolize eATP to adenosine, an immunosuppressive molecule.
- CD39 acts as a critical regulator, modulating the immune response from pro-inflammatory to anti-inflammatory states.
Purpose of the Study:
- To review the current understanding of CD39's role in immunity.
- To comprehensively illustrate the diverse functions of CD39 in various pathological conditions.
Main Methods:
- Literature review of studies on CD39 function in immunity and disease.
- Analysis of the enzymatic cascade involving CD39 and CD73.
- Examination of CD39 expression in different immune cells and its regulation.
Main Results:
- CD39 is a rate-limiting enzyme in the eATP to adenosine pathway.
- CD39 expression is found on various immune cells and influenced by multiple factors.
- CD39 is implicated in the pathophysiology of inflammatory bowel disease, sepsis, multiple sclerosis, and other disorders.
Conclusions:
- CD39 plays a pivotal role as an immunological switch.
- Understanding CD39 function is crucial for developing therapeutic strategies for inflammatory and autoimmune diseases.
- Further research into CD39's diverse roles in pathology is warranted.
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