Influence of adipose tissue immune dysfunction on childhood obesity. (June 2022)
- Record Type:
- Journal Article
- Title:
- Influence of adipose tissue immune dysfunction on childhood obesity. (June 2022)
- Main Title:
- Influence of adipose tissue immune dysfunction on childhood obesity
- Authors:
- Dai, Wanlin
Liu, Xiyan
Su, Han
Li, Xuan
Xu, Yingxi
Yu, Yang - Abstract:
- Abstract: In recent decades, a dramatic rise has been observed in the prevalence of obesity in childhood and adolescence, along with an increase in fetal microsomia rates. The increased risk of obesity during this key period in development negatively affects the health of the individual later in life. Immune cells residing and recruited to white adipose tissue have been highlighted as important factors contributing to the pathogenesis of childhood obesity. Immune dysfunction in the context of obesity begins early in childhood, which is different from the pathological characteristics and influencing factors of adipose immunity in adults. Here, we explore the current understanding of the roles of childhood and early life events that result in high risks for obesity by influencing adipose tissue immune dysfunction under the pathological condition of obesity. Such knowledge will help in determining the mechanisms of childhood and early life obesity in efforts to ameliorate chronic inflammation-related metabolic diseases. Graphical Abstract: Overview of influence of adipose tissue immune dysfunction on childhood obesity. Obesity in childhood and early life lies in both genetic predisposition and obesogenic nurturing environment. Initially, unhealthy lifestyles, such as poor dietary patterns, insufficient exercise, and inadequate sleep, are proved to be negative factors for obesity prevention from an early age. Next in importance, the variety of obesity-related genomic alterationsAbstract: In recent decades, a dramatic rise has been observed in the prevalence of obesity in childhood and adolescence, along with an increase in fetal microsomia rates. The increased risk of obesity during this key period in development negatively affects the health of the individual later in life. Immune cells residing and recruited to white adipose tissue have been highlighted as important factors contributing to the pathogenesis of childhood obesity. Immune dysfunction in the context of obesity begins early in childhood, which is different from the pathological characteristics and influencing factors of adipose immunity in adults. Here, we explore the current understanding of the roles of childhood and early life events that result in high risks for obesity by influencing adipose tissue immune dysfunction under the pathological condition of obesity. Such knowledge will help in determining the mechanisms of childhood and early life obesity in efforts to ameliorate chronic inflammation-related metabolic diseases. Graphical Abstract: Overview of influence of adipose tissue immune dysfunction on childhood obesity. Obesity in childhood and early life lies in both genetic predisposition and obesogenic nurturing environment. Initially, unhealthy lifestyles, such as poor dietary patterns, insufficient exercise, and inadequate sleep, are proved to be negative factors for obesity prevention from an early age. Next in importance, the variety of obesity-related genomic alterations is extensive and is still being studied. What's more, there are particularly obvious correlations between adiposity at birth or infancy and the progression of obesity or metabolic diseases across the whole life stages. Maternal obesity, exposure to endocrine disruptors during pregnancy, and insufficient breastfeeding possibly result in dysfunctional adipose tissue and defective immune function during the very early stages of life, and even lasting until adulthood. Finally, dysregulation of gut microbiota is regarded as an early trigger to the development of obesity and related systemic low-grade inflammation. Interactions between gut microbiota alterations and lipid dysmetabolism plays an important role in individual subsequent adipose tissue development and exerting immune or endocrine function. ga1 Highlights: Adipose immune function is defined in early stage of life, and its disorder will lead to a series of chronic diseases in adulthood. Cytokines derived by obese adipose immune cells aggravate insulin resistance and the whitening of brown and beige adipocytes. Unhealthy lifestyles play key roles in childhood obesity by affecting adipose immunity. … (more)
- Is Part Of:
- Cytokine & growth factor reviews. Volume 65(2022)
- Journal:
- Cytokine & growth factor reviews
- Issue:
- Volume 65(2022)
- Issue Display:
- Volume 65, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 65
- Issue:
- 2022
- Issue Sort Value:
- 2022-0065-2022-0000
- Page Start:
- 27
- Page End:
- 38
- Publication Date:
- 2022-06
- Subjects:
- ANT-2 adenine nucleotide translocase-2 -- ATDC adipose tissue dendritic cell -- ATM adipose tissue macrophage -- BAT brown adipose tissue -- cDC conventional DC -- CLS crown-like structure -- CRP C-reactive protein -- DC dendritic cell -- EAA essential amino acid -- EDC endocrine-disrupting chemical -- GLUT4 glucose transporter 4 -- HFD high-fat diet -- HIF-1α hypoxia-inducible factor-1α -- IFN-γ interferon-γ -- IL-6 interleukin 6 -- IRS-1 insulin receptor substrate-1 -- JNK c-Jun N-terminal kinase -- KLF4 kruppel-like factor 4 -- MAIT cell mucosa associated invariant T cell -- MAPK mitogen activated protein kinase -- MetS metabolic syndrome -- MHC-II class II major histocompatibility complex -- NCR1 NK-cell-activating receptor -- NK cell natural killer cell -- NF-κB nuclear factor kappa beta -- pDC plasmacytoid DC -- PPARγ peroxisome proliferator-activated receptor γ -- RBP4 retinol binding protein 4 -- RXR retinoic acid X receptor -- SAT subcutaneous adipose tissue -- SNP single-nucleotide polymorphism -- TNF-α tumor necrosis factor-α -- Treg cell regulatory T cell -- UCP-1 uncoupling protein-1 -- WAT white adipose tissue
Childhood obesity -- Adipose immunity -- Inflammation -- Early life events
Cytokines -- Periodicals
571.84 - Journal URLs:
- http://www.sciencedirect.com/science/journal/13596101 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.cytogfr.2022.04.008 ↗
- Languages:
- English
- ISSNs:
- 1359-6101
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3506.778500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21559.xml