Abstract

Mast cells (MCs) are an evolutionary well-conserved type of cells, mediating and modulating allergic responses in innate immunity and tissue remodeling after chronic inflammation. Among other tissues, they inhabit both the testis and epididymis. In the testis, MCs usually appear in the interstitial compartment in humans, but not in other standard experimental models, like rats and mice. MCs seem to be responsible for testicular tissue fibrosis in different causes of infertility. Although experimental animal models follow the effect on MC activation or penetration to the interstitial tissue like in humans to some extent, there is an inconsistency in the available literature regarding experimental design, animal strain, and detection methods used. This comprehensive review offers an insight into the literature on MCs in mammalian testes and epididymides. We aimed to find the most suitable model for research on MC and offer recommendations for future experimental designs. When using in vivo animal models, tunica albuginea incorporation and standard histological assessment need to be included. Domesticated boar strains kept in modified controlled conditions exhibit the highest similarity to the MC distribution in the human testis. 3D testicular models are promising but need further fine-tuning to become a valid model for MC investigation.

Highlights

  • Mast cells (MCs) have a crucial role in promoting hypersensitivity reactions and reactions to parasitic diseases

  • Mast cell precursor population originates at the yolk sac [4], while in adult tissues, MC precursors reside in the bone marrow and migrate to tissues where they further differentiate and serve as sentinel cells under the influence of intrinsic and external stimuli [5]

  • There is a great interest in finding an animal or in vitro model, which could be used in experiments analyzing the impact of various stimuli on MC activation

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Summary

Introduction

Mast cells (MCs) have a crucial role in promoting hypersensitivity reactions and reactions to parasitic diseases. They are essential in developing autoimmune diseases, promoting acute and chronic inflammatory responses [1,2], and recognized as critical regulators of immune modulation, capable of suppressing allergic reactions and chronic inflammation [3]. Mast cell hematopoietic progenitors express CD34+ on their surface, and both KIT (type III receptor tyrosine kinase, CD117) and interleukin (IL) 3 initiate their differentiation in the bone marrow [6,7]. C-kit, which encodes for KIT (CD117), is essential in regulating all aspects of MC biology besides differentiation: survival, proliferation, secretory functions, and migration. Unlike MCs, most hematopoietic cells lose their KIT expression in the process of differentiation. The stem cell factor (SCF) functions as its specific ligand and has several other names—steel factor, MC growth factor, or, most

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