新冠肺炎大流行期间环境压力的变化可能导致与Krtcap3相关的肥胖表型复制失败。

IF 2.5 4区 生物学 Q3 CELL BIOLOGY
Physiological genomics Pub Date : 2023-10-01 Epub Date: 2023-07-17 DOI:10.1152/physiolgenomics.00019.2023
Alexandria M Szalanczy, Gina Giorgio, Emily Goff, Osborne Seshie, Michael Grzybowski, Jason Klotz, Aron M Geurts, Eva E Redei, Leah C Solberg Woods
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引用次数: 0

摘要

我们之前在雌性大鼠中鉴定了角质形成细胞相关蛋白3 Krtcap3是一种肥胖相关基因,当喂食高脂饮食(HFD)时,与野生型(WT)对照相比,全身Krtcap3-敲除(KO)导致肥胖增加。我们试图复制这项工作,以更好地理解Krtcap3的功能,但无法复制肥胖表型。在目前的研究中,与先前研究中的WT相比,WT雌性大鼠吃得更多,体重和脂肪量相应增加,而KO雌性大鼠的这些指标在研究之间没有变化。先前的研究是在新冠肺炎大流行之前进行的,而当前的研究是从最初的封锁令之后开始的,并在大流行期间在通常压力较小的环境中完成。我们假设环境变化影响了压力水平,并可能解释未能复制我们的结果。安乐死时皮质酮(CORT)的分析显示,通过基因型相互作用进行的一项重要研究表明,在研究1中,WT的CORT显著高于KO,在研究2中没有差异。这些数据表明,降低Krtcap3的表达可能会改变环境应激反应,从而影响肥胖。我们还发现,在这两项研究中,KO大鼠(而不是WT)在其笼友被移除后,CORT显著增加,这表明它们与社会行为压力有单独的联系。未来的工作有必要证实和阐明这些关系的精细机制,但这些数据表明Krtcap3有可能成为一种新的应激基因。新的和值得注意的肥胖与遗传和压力等环境因素有关。Krtcap3先前已被鉴定为与肥胖相关的基因,我们在这里的工作表明,环境压力可能影响Krtcap3-在食物摄入和肥胖中的作用。肥胖在很大程度上受到人类压力的影响,因此识别出将压力和肥胖联系起来的新基因将大大促进我们对这种疾病的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Changes in environmental stress over COVID-19 pandemic likely contributed to failure to replicate adiposity phenotype associated with Krtcap3.

We previously identified keratinocyte-associated protein 3, Krtcap3, as an obesity-related gene in female rats where a whole body Krtcap3 knockout (KO) led to increased adiposity compared to wild-type (WT) controls when fed a high-fat diet (HFD). We sought to replicate this work to better understand the function of Krtcap3 but were unable to reproduce the adiposity phenotype. In the current work, WT female rats ate more compared to WT in the prior study, with corresponding increases in body weight and fat mass, while there were no changes in these measures in KO females between the studies. The prior study was conducted before the COVID-19 pandemic, while the current study started after initial lockdown orders and was completed during the pandemic in a generally less stressful environment. We hypothesize that the environmental changes impacted stress levels and may explain the failure to replicate our results. Analysis of corticosterone (CORT) at euthanasia showed a significant study-by-genotype interaction where WT had significantly higher CORT relative to KO in study 1, with no differences in study 2. These data suggest that decreasing Krtcap3 expression may alter the environmental stress response to influence adiposity. We also found that KO rats in both studies, but not WT, experienced a dramatic increase in CORT after their cage mate was removed, suggesting a separate connection to social behavioral stress. Future work is necessary to confirm and elucidate the finer mechanisms of these relationships, but these data indicate the possibility of Krtcap3 as a novel stress gene.NEW & NOTEWORTHY Obesity is linked to both genetics and environmental factors such as stress. Krtcap3 has previously been identified as a gene associated with adiposity, and our work here demonstrates that environmental stress may influence the role of Krtcap3 on both food intake and adiposity. Obesity is strongly influenced by stress in humans, so the identification of novel genes that link stress and obesity will greatly advance our understanding of the disease.

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来源期刊
Physiological genomics
Physiological genomics 生物-生理学
CiteScore
6.10
自引率
0.00%
发文量
46
审稿时长
4-8 weeks
期刊介绍: The Physiological Genomics publishes original papers, reviews and rapid reports in a wide area of research focused on uncovering the links between genes and physiology at all levels of biological organization. Articles on topics ranging from single genes to the whole genome and their links to the physiology of humans, any model organism, organ, tissue or cell are welcome. Areas of interest include complex polygenic traits preferably of importance to human health and gene-function relationships of disease processes. Specifically, the Journal has dedicated Sections focused on genome-wide association studies (GWAS) to function, cardiovascular, renal, metabolic and neurological systems, exercise physiology, pharmacogenomics, clinical, translational and genomics for precision medicine, comparative and statistical genomics and databases. For further details on research themes covered within these Sections, please refer to the descriptions given under each Section.
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