
Endothelial microvesicles in hypoxic hypoxia diseases
Author(s) -
Deng Fan,
Wang Shuang,
Xu Riping,
Yu Wenqian,
Wang Xianyu,
Zhang Liangqing
Publication year - 2018
Publication title -
journal of cellular and molecular medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.44
H-Index - 130
eISSN - 1582-4934
pISSN - 1582-1838
DOI - 10.1111/jcmm.13671
Subject(s) - hypoxia (environmental) , microvesicles , medicine , immunology , biology , chemistry , microrna , biochemistry , oxygen , organic chemistry , gene
Hypoxic hypoxia, including abnormally low partial pressure of inhaled oxygen, external respiratory dysfunction‐induced respiratory hypoxia and venous blood flow into the arterial blood, is characterized by decreased arterial oxygen partial pressure, resulting in tissue oxygen deficiency. The specific characteristics include reduced arterial oxygen partial pressure and oxygen content. Hypoxic hypoxia diseases ( HHD s) have attracted increased attention due to their high morbidity and mortality and mounting evidence showing that hypoxia‐induced oxidative stress, coagulation, inflammation and angiogenesis play extremely important roles in the physiological and pathological processes of HHD s‐related vascular endothelial injury. Interestingly, endothelial microvesicles ( EMV s), which can be induced by hypoxia, hypoxia‐induced oxidative stress, coagulation and inflammation in HHD s, have emerged as key mediators of intercellular communication and cellular functions. EMV s shed from activated or apoptotic endothelial cells ( EC s) reflect the degree of EC s damage, and elevated EMV s levels are present in several HHD s, including obstructive sleep apnoea syndrome and chronic obstructive pulmonary disease. Furthermore, EMV s have procoagulant, proinflammatory and angiogenic functions that affect the pathological processes of HHD s. This review summarizes the emerging roles of EMV s in the diagnosis, staging, treatment and clinical prognosis of HHD s.