家鸡(Gallus domesticus)对脂多糖的急性期反应中,蜕皮抑制促炎细胞因子的产生。

IF 2.4 3区 农林科学 Q1 FISHERIES
A.M. DeRogatis, R.A. Hernandez, J.C. Suico, K.C. Klasing
{"title":"家鸡(Gallus domesticus)对脂多糖的急性期反应中,蜕皮抑制促炎细胞因子的产生。","authors":"A.M. DeRogatis,&nbsp;R.A. Hernandez,&nbsp;J.C. Suico,&nbsp;K.C. Klasing","doi":"10.1016/j.dci.2025.105461","DOIUrl":null,"url":null,"abstract":"<div><div>There are a variety of nutritionally costly life stages that birds must balance with investments in the immune system, yet much remains unknown about how the process of molt impacts immunity. For chickens, similar to other birds, molt is characterized by periodic feather shedding and replacement along with broader physiological changes like reproductive quiescent. To investigate how molt modulates innate immunity, mRNA expression and the plasma concentration of key cytokines were evaluated following an acute phase response induced by lipopolysaccharide (LPS-APR). Laying hens were challenged with an intraperitoneal injection of LPS at 1.5 mg/kg of body weight during the peak feather production period of an induced molt. Cytokine expression was evaluated in the liver, spleen, and plasma 4 h post-injection. Molting hens had reduced expression of certain pro-inflammatory cytokines, with the most significant reduction occurring in expression of IL-6 in the liver. This trend occurred even when the number of molted feathers varied in the fully feather UCD-003 or sparsely feathered Scaleless High hens. Importantly, molting hens failed to significantly increase plasma levels of IL-1β and IL-6 to those observed in the non-molting birds in response to LPS. A reduction in the expression of key pro-inflammatory cytokines, especially those involved in the febrile response and hepatic immune function, suggest that molt may reduce the availability of nutrients and energy needed to support the acute phase response to LPS. This attenuation is likely a mechanism to allow both molt and an innate immune response to progress during an energetic or nutritional bottleneck.</div></div>","PeriodicalId":11228,"journal":{"name":"Developmental and comparative immunology","volume":"172 ","pages":"Article 105461"},"PeriodicalIF":2.4000,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Molt dampens pro-inflammatory cytokine production during the acute phase response to lipopolysaccharide in the domestic chicken (Gallus domesticus)\",\"authors\":\"A.M. DeRogatis,&nbsp;R.A. Hernandez,&nbsp;J.C. Suico,&nbsp;K.C. Klasing\",\"doi\":\"10.1016/j.dci.2025.105461\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>There are a variety of nutritionally costly life stages that birds must balance with investments in the immune system, yet much remains unknown about how the process of molt impacts immunity. For chickens, similar to other birds, molt is characterized by periodic feather shedding and replacement along with broader physiological changes like reproductive quiescent. To investigate how molt modulates innate immunity, mRNA expression and the plasma concentration of key cytokines were evaluated following an acute phase response induced by lipopolysaccharide (LPS-APR). Laying hens were challenged with an intraperitoneal injection of LPS at 1.5 mg/kg of body weight during the peak feather production period of an induced molt. Cytokine expression was evaluated in the liver, spleen, and plasma 4 h post-injection. Molting hens had reduced expression of certain pro-inflammatory cytokines, with the most significant reduction occurring in expression of IL-6 in the liver. This trend occurred even when the number of molted feathers varied in the fully feather UCD-003 or sparsely feathered Scaleless High hens. Importantly, molting hens failed to significantly increase plasma levels of IL-1β and IL-6 to those observed in the non-molting birds in response to LPS. A reduction in the expression of key pro-inflammatory cytokines, especially those involved in the febrile response and hepatic immune function, suggest that molt may reduce the availability of nutrients and energy needed to support the acute phase response to LPS. This attenuation is likely a mechanism to allow both molt and an innate immune response to progress during an energetic or nutritional bottleneck.</div></div>\",\"PeriodicalId\":11228,\"journal\":{\"name\":\"Developmental and comparative immunology\",\"volume\":\"172 \",\"pages\":\"Article 105461\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2025-09-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Developmental and comparative immunology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0145305X25001508\",\"RegionNum\":3,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"FISHERIES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Developmental and comparative immunology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0145305X25001508","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"FISHERIES","Score":null,"Total":0}
引用次数: 0

摘要

鸟类必须在免疫系统的投资中平衡各种营养昂贵的生命阶段,但关于蜕皮过程如何影响免疫力,仍有很多未知。对于鸡来说,与其他鸟类相似,蜕皮的特征是周期性的羽毛脱落和替换,以及更广泛的生理变化,如生殖静止。为了研究蜕皮对先天免疫的调节作用,在脂多糖(LPS-APR)诱导的急性期反应后,研究了mRNA表达和血浆中关键细胞因子的浓度。在诱导蜕皮的产羽高峰期,蛋鸡腹腔注射1.5 mg/kg体重的LPS。注射后4小时检测肝脏、脾脏和血浆中细胞因子的表达。换羽母鸡某些促炎细胞因子的表达降低,其中肝脏中IL-6的表达降低最为显著。即使在全羽UCD-003或稀疏羽无鳞高蛋鸡的蜕皮羽毛数量发生变化时,这种趋势也发生了。重要的是,在LPS的作用下,蜕皮母鸡血浆中IL-1β和IL-6的水平并没有提高。关键促炎细胞因子的表达减少,特别是那些参与发热反应和肝脏免疫功能的细胞因子的表达减少,表明蜕皮可能减少了支持LPS急性期反应所需的营养和能量的可用性。这种衰减可能是一种机制,允许蜕皮和先天免疫反应在能量或营养瓶颈期间取得进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molt dampens pro-inflammatory cytokine production during the acute phase response to lipopolysaccharide in the domestic chicken (Gallus domesticus)
There are a variety of nutritionally costly life stages that birds must balance with investments in the immune system, yet much remains unknown about how the process of molt impacts immunity. For chickens, similar to other birds, molt is characterized by periodic feather shedding and replacement along with broader physiological changes like reproductive quiescent. To investigate how molt modulates innate immunity, mRNA expression and the plasma concentration of key cytokines were evaluated following an acute phase response induced by lipopolysaccharide (LPS-APR). Laying hens were challenged with an intraperitoneal injection of LPS at 1.5 mg/kg of body weight during the peak feather production period of an induced molt. Cytokine expression was evaluated in the liver, spleen, and plasma 4 h post-injection. Molting hens had reduced expression of certain pro-inflammatory cytokines, with the most significant reduction occurring in expression of IL-6 in the liver. This trend occurred even when the number of molted feathers varied in the fully feather UCD-003 or sparsely feathered Scaleless High hens. Importantly, molting hens failed to significantly increase plasma levels of IL-1β and IL-6 to those observed in the non-molting birds in response to LPS. A reduction in the expression of key pro-inflammatory cytokines, especially those involved in the febrile response and hepatic immune function, suggest that molt may reduce the availability of nutrients and energy needed to support the acute phase response to LPS. This attenuation is likely a mechanism to allow both molt and an innate immune response to progress during an energetic or nutritional bottleneck.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
6.20
自引率
6.90%
发文量
206
审稿时长
49 days
期刊介绍: Developmental and Comparative Immunology (DCI) is an international journal that publishes articles describing original research in all areas of immunology, including comparative aspects of immunity and the evolution and development of the immune system. Manuscripts describing studies of immune systems in both vertebrates and invertebrates are welcome. All levels of immunological investigations are appropriate: organismal, cellular, biochemical and molecular genetics, extending to such fields as aging of the immune system, interaction between the immune and neuroendocrine system and intestinal immunity.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信