TY - JOUR
T1 - Beyond the neuron
T2 - Role of non-neuronal cells in stress disorders
AU - Cathomas, Flurin
AU - Holt, Leanne M.
AU - Parise, Eric M.
AU - Liu, Jia
AU - Murrough, James W.
AU - Casaccia, Patrizia
AU - Nestler, Eric J.
AU - Russo, Scott J.
N1 - Funding Information:
Preparation of this review was supported by NIH grants R01MH114882-01 , R01MH104559 , and R01MH127820 (S.J.R.); P50MH096890 and R01MH051399 (E.J.N.); and R35NS111604 (P.C.); the Swiss National Science Foundation ( P400PM_186708 ) (F.C.); the Brain & Behavior Research Foundation ( 29104 ) (F.C.); the Brain & Behavior Research Foundation (30609) (E.M.P); and NINDS R35NS111604 (P.C.) . We would like to thank Ms. Ni-ka Ford, academic medical illustrator for the Icahn School of Medicine at Mount Sinai, for generating the figures for this review.
Funding Information:
Preparation of this review was supported by NIH grants R01MH114882-01, R01MH104559, and R01MH127820 (S.J.R.); P50MH096890 and R01MH051399 (E.J.N.); and R35NS111604 (P.C.); the Swiss National Science Foundation (P400PM_186708) (F.C.); the Brain & Behavior Research Foundation (29104) (F.C.); the Brain & Behavior Research Foundation (30609) (E.M.P); and NINDS R35NS111604 (P.C.). We would like to thank Ms. Ni-ka Ford, academic medical illustrator for the Icahn School of Medicine at Mount Sinai, for generating the figures for this review. The authors declare no competing interests.
Publisher Copyright:
© 2022 Elsevier Inc.
PY - 2022/4/6
Y1 - 2022/4/6
N2 - Stress disorders are leading causes of disease burden in the U.S. and worldwide, yet available therapies are fully effective in less than half of all individuals with these disorders. Although to date, much of the focus has been on neuron-intrinsic mechanisms, emerging evidence suggests that chronic stress can affect a wide range of cell types in the brain and periphery, which are linked to maladaptive behavioral outcomes. Here, we synthesize emerging literature and discuss mechanisms of how non-neuronal cells in limbic regions of brain interface at synapses, the neurovascular unit, and other sites of intercellular communication to mediate the deleterious, or adaptive (i.e., pro-resilient), effects of chronic stress in rodent models and in human stress-related disorders. We believe that such an approach may one day allow us to adopt a holistic “whole body” approach to stress disorder research, which could lead to more precise diagnostic tests and personalized treatment strategies. Stress is a major risk factor for many psychiatric disorders. Cathomas et al. review new insight into how non-neuronal cells mediate the deleterious effects, as well as the adaptive, protective effects, of stress in rodent models and human stress-related disorders.
AB - Stress disorders are leading causes of disease burden in the U.S. and worldwide, yet available therapies are fully effective in less than half of all individuals with these disorders. Although to date, much of the focus has been on neuron-intrinsic mechanisms, emerging evidence suggests that chronic stress can affect a wide range of cell types in the brain and periphery, which are linked to maladaptive behavioral outcomes. Here, we synthesize emerging literature and discuss mechanisms of how non-neuronal cells in limbic regions of brain interface at synapses, the neurovascular unit, and other sites of intercellular communication to mediate the deleterious, or adaptive (i.e., pro-resilient), effects of chronic stress in rodent models and in human stress-related disorders. We believe that such an approach may one day allow us to adopt a holistic “whole body” approach to stress disorder research, which could lead to more precise diagnostic tests and personalized treatment strategies. Stress is a major risk factor for many psychiatric disorders. Cathomas et al. review new insight into how non-neuronal cells mediate the deleterious effects, as well as the adaptive, protective effects, of stress in rodent models and human stress-related disorders.
UR - http://www.scopus.com/inward/record.url?scp=85125788642&partnerID=8YFLogxK
U2 - 10.1016/j.neuron.2022.01.033
DO - 10.1016/j.neuron.2022.01.033
M3 - Review article
C2 - 35182484
AN - SCOPUS:85125788642
SN - 0896-6273
VL - 110
SP - 1116
EP - 1138
JO - Neuron
JF - Neuron
IS - 7
ER -