TY - JOUR
T1 - The diversity and coexistence of extracellular mitochondria in circulation
T2 - A friend or foe of the immune system
AU - Caicedo, Andrés
AU - Zambrano, Kevin
AU - Sanon, Serena
AU - Luis Vélez, Jorge
AU - Montalvo, Mario
AU - Jara, Fernando
AU - Moscoso, Santiago Aguayo
AU - Vélez, Pablo
AU - Maldonado, Augusto
AU - Velarde, Gustavo
N1 - Publisher Copyright:
© 2021 Elsevier B.V. and Mitochondria Research Society. All rights reserved.
PY - 2021/5
Y1 - 2021/5
N2 - The diversity and coexistence of extracellular mitochondria may have a key role in the maintenance of health and progression of disease. Studies report that active mitochondria can be found physiologically outside of cells and circulating in the blood without inducing an inflammatory response. In addition, inactive or harmed mitochondria have been recognized as activators of immune cells, as they play an essential role in diseases characterized by the metabolic deregulation of these cells, such as sepsis. In this review we analyze key aspects regarding the existence of a diversity of extracellular mitochondria, their coexistence in body fluids and their effects on various immune cells. Additionally, we introduce models of how extracellular mitochondria could be interacting to maintain health and affect disease prognosis. Unwrapped mitochondria (freeMitos) can exist as viable, active, inactive or harmed organelles. Mitochondria can also be found wrapped in a membrane (wrappedMitos) that may differ depending on the cell of origin. Mitochondrial fragments can also be present in various body fluids as DAMPs, as mtDNA enclosed in vesicles or as circulating-cell-free mtDNA (ccf-mtDNA). Interestingly, the great quantity of evidence regarding the levels of ccf-mtDNA and their correlation with aging and disease allows for the identification of the diversity, but not type, of extracellular mitochondria. The existence of a diversity of mitochondria and their effects on immune cells opens a new concept in the biomedical field towards the understanding of health, the progression of disease and the development of mitochondria as therapeutic agents.
AB - The diversity and coexistence of extracellular mitochondria may have a key role in the maintenance of health and progression of disease. Studies report that active mitochondria can be found physiologically outside of cells and circulating in the blood without inducing an inflammatory response. In addition, inactive or harmed mitochondria have been recognized as activators of immune cells, as they play an essential role in diseases characterized by the metabolic deregulation of these cells, such as sepsis. In this review we analyze key aspects regarding the existence of a diversity of extracellular mitochondria, their coexistence in body fluids and their effects on various immune cells. Additionally, we introduce models of how extracellular mitochondria could be interacting to maintain health and affect disease prognosis. Unwrapped mitochondria (freeMitos) can exist as viable, active, inactive or harmed organelles. Mitochondria can also be found wrapped in a membrane (wrappedMitos) that may differ depending on the cell of origin. Mitochondrial fragments can also be present in various body fluids as DAMPs, as mtDNA enclosed in vesicles or as circulating-cell-free mtDNA (ccf-mtDNA). Interestingly, the great quantity of evidence regarding the levels of ccf-mtDNA and their correlation with aging and disease allows for the identification of the diversity, but not type, of extracellular mitochondria. The existence of a diversity of mitochondria and their effects on immune cells opens a new concept in the biomedical field towards the understanding of health, the progression of disease and the development of mitochondria as therapeutic agents.
KW - Biomarker
KW - Extracellular mitochondria
KW - Immunoregulation
KW - Inflammation
KW - Sepsis
KW - Therapeutic agent
UR - http://www.scopus.com/inward/record.url?scp=85104328183&partnerID=8YFLogxK
U2 - 10.1016/j.mito.2021.02.014
DO - 10.1016/j.mito.2021.02.014
M3 - Artículo de revisión
C2 - 33662580
AN - SCOPUS:85104328183
SN - 1567-7249
VL - 58
SP - 270
EP - 284
JO - Mitochondrion
JF - Mitochondrion
ER -