TY - JOUR
T1 - Nitric oxide in cellular adaptation and disease
AU - Gantner, Benjamin N.
AU - LaFond, Katy M.
AU - Bonini, Marcelo G.
N1 - Funding Information:
The authors are grateful for support from the Dr. Nancy Laning Sobczak Fund for Breast Cancer (to BNG), the MCW Cancer Center through the Research and Education Program Fund, a component of the Advancing a Healthier Wisconsin endowment (to BNG and MGB), a grant from the MCW Research Affairs Committee (to BNG), RO1CA216882 (to MGB), RO1AI131267 (to MGB), RO1ES028149 (to MGB), DOD 71138LS (to MGB), the Wisconsin Breast Cancer Showhouse (to MGB and BNG). The authors thank Jennifer Keane for editing and critical reading of the manuscript.
Publisher Copyright:
© 2020 The Authors
PY - 2020/7
Y1 - 2020/7
N2 - Nitric oxide synthases are the major sources of nitric oxide, a critical signaling molecule involved in a wide range of cellular and physiological processes. These enzymes comprise a family of genes that are highly conserved across all eukaryotes. The three family members found in mammals are important for inter- and intra-cellular signaling in tissues that include the nervous system, the vasculature, the gut, skeletal muscle, and the immune system, among others. We summarize major advances in the understanding of biochemical and tissue-specific roles of nitric oxide synthases, with a focus on how these mechanisms enable tissue adaptation and health or dysfunction and disease. We highlight the unique mechanisms and processes of neuronal nitric oxide synthase, or NOS1. This was the first of these enzymes discovered in mammals, and yet much remains to be understood about this highly conserved and complex gene. We provide examples of two areas that will likely be of increasing importance in nitric oxide biology. These include the mechanisms by which these critical enzymes promote adaptation or disease by 1) coordinating communication by diverse cell types within a tissue and 2) directing cellular differentiation/activation decisions processes.
AB - Nitric oxide synthases are the major sources of nitric oxide, a critical signaling molecule involved in a wide range of cellular and physiological processes. These enzymes comprise a family of genes that are highly conserved across all eukaryotes. The three family members found in mammals are important for inter- and intra-cellular signaling in tissues that include the nervous system, the vasculature, the gut, skeletal muscle, and the immune system, among others. We summarize major advances in the understanding of biochemical and tissue-specific roles of nitric oxide synthases, with a focus on how these mechanisms enable tissue adaptation and health or dysfunction and disease. We highlight the unique mechanisms and processes of neuronal nitric oxide synthase, or NOS1. This was the first of these enzymes discovered in mammals, and yet much remains to be understood about this highly conserved and complex gene. We provide examples of two areas that will likely be of increasing importance in nitric oxide biology. These include the mechanisms by which these critical enzymes promote adaptation or disease by 1) coordinating communication by diverse cell types within a tissue and 2) directing cellular differentiation/activation decisions processes.
KW - Adaptation
KW - Intercellular signaling
KW - Intracellular signaling
KW - Nitic oxide synthase
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U2 - 10.1016/j.redox.2020.101550
DO - 10.1016/j.redox.2020.101550
M3 - Review article
C2 - 32438317
AN - SCOPUS:85084644297
SN - 2213-2317
VL - 34
JO - Redox Biology
JF - Redox Biology
M1 - 101550
ER -