Immunomodulatory properties of medicinal mushrooms: differential effects of water and ethanol extracts on NK cell-mediated cytotoxicity.

Innate Immun

Center for Molecular and Clinical Immunology, Chang Gung University, Taoyuan, Taiwan, Republic of China Laboratory of Nanomaterials, Chang Gung University, Taoyuan, Taiwan, Republic of China Chang Gung Biotechnology Corporation, Taipei, Taiwan, Republic of China Biochemical Engineering Research Center, Ming Chi University of Technology, New Taipei City, Taiwan, Republic of China Laboratory of Cellular Physiology and Immunology, Rockefeller University, New York, NY, USA

Published: October 2016

Medicinal mushrooms have been used for centuries in Asian countries owing to their beneficial effects on health and longevity. Previous studies have reported that a single medicinal mushroom may produce both stimulatory and inhibitory effects on immune cells, depending on conditions, but the factors responsible for this apparent dichotomy remain obscure. We show here that water and ethanol extracts of cultured mycelium from various species (Agaricus blazei Murrill, Antrodia cinnamomea, Ganoderma lucidum and Hirsutella sinensis) produce opposite effects on NK cells. Water extracts enhance NK cell cytotoxic activity against cancer cells, whereas ethanol extracts inhibit cytotoxicity. Water extracts stimulate the expression and production of cytolytic proteins (perforin and granulysin) and NKG2D/NCR cell surface receptors, and activate intracellular signaling kinases (ERK, JNK and p38). In contrast, ethanol extracts inhibit expression of cytolytic and cell surface receptors. Our results suggest that the mode of extraction of medicinal mushrooms may determine the nature of the immunomodulatory effects produced on immune cells, presumably owing to the differential solubility of stimulatory and inhibitory mediators. These findings have important implications for the preparation of medicinal mushrooms to prevent and treat human diseases.

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Source
http://dx.doi.org/10.1177/1753425916661402DOI Listing

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