Mast Cells as a Potential Target of Molecular Hydrogen in Regulating the Local Tissue Microenvironment

Knowledge of the biological effects of molecular hydrogen (H2), hydrogen gas, is constantly advancing, giving a reason for the optimism in several healthcare practitioners regarding the management of multiple diseases, including socially significant ones (malignant neoplasms, diabetes mellitus, viral hepatitis, mental and behavioral disorders). However, mechanisms underlying the biological effects of H2 are still being actively debated. In this review, we focus on mast cells as a potential target for H2 at the specific tissue microenvironment level. H2 regulates the processing of pro-inflammatory components of the mast cell secretome and their entry into the extracellular matrix; this can significantly affect the capacity of the integrated-buffer metabolism and the structure of the immune landscape of the local tissue microenvironment. The analysis performed highlights several potential mechanisms for developing the biological effects of H2 and offers great opportunities for translating the obtained findings into clinical practice. © 2023 by the authors.

Авторы
Atiakshin D. , Kostin A. , Volodkin A. , Nazarova A. , Shishkina V. , Esaulenko D. , Buchwalow I. , Tiemann M. , Noda M.
Журнал
Издательство
MDPI AG
Номер выпуска
6
Язык
Английский
Статус
Опубликовано
Номер
817
Том
16
Год
2023
Организации
  • 1 Research and Educational Resource Center for Immunophenotyping, Digital Spatial Profiling and Ultrastructural Analysis Innovative Technologies, Peoples’ Friendship University of Russia Named after Patrice Lumumba, Moscow, 117198, Russian Federation
  • 2 Research Institute of Experimental Biology and Medicine, Burdenko Voronezh State Medical University, Voronezh, 394036, Russian Federation
  • 3 Institute for Hematopathology, Fangdieckstr. 75a, Hamburg, 22547, Germany
  • 4 Laboratory of Pathophysiology, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, 816-0811, Japan
Ключевые слова
inflammation; local tissue microenvironment; mast cells; molecular hydrogen; reactive oxygen intermediates; secretome; specific mast cell proteases
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