Ultrastructural features of tumor‐associated mast cells in parasympathetic paragangliomas (chemodectomas) of the neck

Author:

Chekmaryova Irina12ORCID,Kalinin Dmitry1ORCID,Kostin Andrey2ORCID,Buchwalow Igor23ORCID,Tiemann Markus3ORCID,Elieh‐Ali‐Komi Daniel45ORCID,Atiakshin Dmitrii26ORCID

Affiliation:

1. Federal State Budgetary Institution “National Medical Research Center of Surgery named after A. Vishnevsky” Ministry of Health of the Russian Federation Moscow Russia

2. Research and Educational Resource Center for Immunophenotyping, Digital Spatial Profiling and Ultrastructural Analysis Innovative Technologies Peoples' Friendship University of Russia Moscow Russia

3. Institute for Hematopathology Hamburg Germany

4. Institute of Allergology, Charité—Universitätsmedizin Berlin Freie Universität Berlin and Humboldt‐Universität zu Berlin Berlin Germany

5. Allergology and Immunology Fraunhofer Institute for Translational Medicine and Pharmacology ITMP Berlin Germany

6. Research Institute of Experimental Biology and Medicine Burdenko Voronezh State Medical University Voronezh Russia

Abstract

AbstractThe mechanisms of the pathogenesis of neck paraganglioma (PGL) and the possible role of mast cells (MCs) in its development and metastasis are still poorly understood. We analyzed MCs' morphologic characterization, activation, and the properties of their cytoplasmic/released granules in PGLs, using light and transmission electron microscopy. Paragangliomas showed a large tumor‐associated MC population both in the connective tissue layers of the tumor and between the tumor cells. Notably, MCs were presented by a high expression of specific proteases, size variation, polymorphism, and variable ultrastructural phenotype of granules. A massive number of granules were released surrounding the degranulated MCs while the integrity of MC membrane was maintained. Granules were electron‐dense with or without a membrane, ranging from 0.2 to 0.8 μm in diameter. MC plasmalemma was not found at the site of MC‐collagen fibrils contact, whereas the secretome and fibrils were directly contacted. We observed direct and mediator‐based interactions between MCs and paraganglioma cells. The latter preserved their membrane integrity when MC granules were not in proximity. The effects of the MC secretome on the paraganglioma microenvironment demonstrated its pathogenetic role in tumor progression and allow its application to new diagnostic criteria and the development of protocols for personalized therapy.Research Highlights Ultrastructural analysis reveals novel regulatory effects of mast cells via diverse secretory pathways on the pathogenesis of parasympathetic paraganglioma, including fibrous extracellular matrix remodeling and mediator‐based interactions between MCs and cells of the tumor microenvironment.

Funder

Russian Science Foundation

Publisher

Wiley

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