Affiliation:
1. Institute of Tissue Medicine and Pathology University of Bern Bern Switzerland
2. Graduate School for Cellular and Biomedical Sciences University of Bern Bern Switzerland
Abstract
AbstractPhosphoinositide‐3‐kinase/AKT (PI3K/AKT) signaling plays key roles in the regulation of cellular activity in both health and disease. In immune cells, this PI3K/AKT pathway is critically regulated by the phosphoinositide phosphatase SHIP1, which has been reported to modulate the function of most immune subsets. In this review, we summarize our current knowledge of SHIP1 with a focus on innate immune cells, where we reflect on the most pertinent aspects described in the current literature. We also present several small‐molecule agonists and antagonists of SHIP1 developed over the last two decades, which have led to improved outcomes in several preclinical models of disease. We outline these promising findings and put them in relation to human diseases with unmet medical needs, where we discuss the most attractive targets for immune therapies based on SHIP1 modulation.
Funder
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Lungenliga Schweiz
Subject
Immunology,Immunology and Allergy
Cited by
5 articles.
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