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Mast cells in renal inflammation and fibrosis: Lessons learnt from animal studies

2014; Elsevier BV; Volume: 63; Issue: 1 Linguagem: Inglês

10.1016/j.molimm.2014.03.002

1872-9142

Lydia Celia Madjène, Maguelonne Pons, Luca Danelli, Julien Claver, Liza Ali, Iris K. Madera‐Salcedo, Asma Kassas, Christophe Pellefigues, Florian Marquet, Albert Dadah, Tarik Attout, Alaa El‐Ghoneimi, Grégory Gautier, Marc Benhamou, Nicolas Charles, Éric Daugas, Pierre Launay, Ulrich Blank,

Renal Diseases and Glomerulopathies

Mast cells are hematopoietic cells involved in inflammation and immunity and have been recognized also as important effector cells in kidney inflammation. In humans, only a few mast cells reside in kidneys constitutively but in progressive renal diseases their numbers increase substantially representing an essential part of the interstitial infiltrate of inflammatory cells. Recent data obtained in experimental animal models have emphasized a complex role of these cells and the mediators they release as they have been shown both to promote, but also to protect from disease and fibrosis development. Sometimes conflicting results have been reported in similar models suggesting a very narrow window between these activities depending on the pathophysiological context. Interestingly in mice, mast cell or mast cell mediator specific actions became also apparent in the absence of significant mast cell kidney infiltration supporting systemic or regional actions via draining lymph nodes or kidney capsules. Many of their activities rely on the capacity of mast cells to release, in a timely controlled manner, a wide range of inflammatory mediators, which can promote anti-inflammatory actions and repair activities that contribute to healing, but in some circumstances or in case of inappropriate regulation may also promote kidney disease.