IL-6 regulates adipose deposition and homeostasis in lymphedema

脂肪组织 淋巴系统 淋巴水肿 炎症 平衡 医学 内分泌学 内科学 淋巴管新生 病理 癌症 转移 乳腺癌
作者
Daniel Cuzzone,Evan Weitman,Nicholas J. Albano,Swapna Ghanta,Ira L. Savetsky,Jason C. Gardenier,Walter J. Joseph,Jeremy S. Torrisi,Jacqueline Bromberg,Waldemar L. Olszewski,Stanley G. Rockson,Babak J. Mehrara
出处
期刊:American Journal of Physiology-heart and Circulatory Physiology [American Physical Society]
卷期号:306 (10): H1426-H1434 被引量:79
标识
DOI:10.1152/ajpheart.01019.2013
摘要

Lymphedema (LE) is a morbid disease characterized by chronic limb swelling and adipose deposition. Although it is clear that lymphatic injury is necessary for this pathology, the mechanisms that underlie lymphedema remain unknown. IL-6 is a known regulator of adipose homeostasis in obesity and has been shown to be increased in primary and secondary models of lymphedema. Therefore, the purpose of this study was to determine the role of IL-6 in adipose deposition in lymphedema. The expression of IL-6 was analyzed in clinical tissue specimens and serum from patients with or without LE, as well as in two mouse models of lymphatic injury. In addition, we analyzed IL-6 expression/adipose deposition in mice deficient in CD4 + cells (CD4KO) or IL-6 expression (IL-6KO) or mice treated with a small molecule inhibitor of IL-6 or CD4 depleting antibodies to determine how IL-6 expression is regulated and the effect of changes in IL-6 expression on adipose deposition after lymphatic injury. Patients with LE and mice treated with lymphatic excision of the tail had significantly elevated tissue and serum expression of IL-6 and its downstream mediator. The expression of IL-6 was associated with adipose deposition and CD4 + inflammation and was markedly decreased in CD4KO mice. Loss of IL-6 function resulted in significantly increased adipose deposition after tail lymphatic injury. Our findings suggest that IL-6 is increased as a result of adipose deposition and CD4 + cell inflammation in lymphedema. In addition, our study suggests that IL-6 expression in lymphedema acts to limit adipose accumulation.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
神勇的悟空完成签到,获得积分10
1秒前
anna521212发布了新的文献求助10
1秒前
FODCOC完成签到,获得积分10
1秒前
沧海一笑完成签到 ,获得积分10
2秒前
1499yqq完成签到 ,获得积分10
2秒前
柳惊完成签到,获得积分10
2秒前
xuluo发布了新的文献求助10
2秒前
睡觉不失眠完成签到 ,获得积分10
3秒前
六月完成签到,获得积分10
4秒前
李天磊发布了新的文献求助10
4秒前
故事的小红花完成签到,获得积分10
5秒前
qw发布了新的文献求助10
6秒前
6秒前
哈哈完成签到,获得积分10
6秒前
大个应助悠悠采纳,获得10
6秒前
houxufeng发布了新的文献求助10
6秒前
frankyeah完成签到,获得积分10
8秒前
8秒前
zhangxin发布了新的文献求助10
9秒前
共享精神应助晚风采纳,获得10
9秒前
蒋彩艳完成签到 ,获得积分10
9秒前
柠檬草完成签到,获得积分10
10秒前
感动白开水完成签到,获得积分10
11秒前
积极行天完成签到,获得积分10
12秒前
12秒前
gg完成签到,获得积分10
13秒前
wwawi完成签到,获得积分10
13秒前
13秒前
FI发布了新的文献求助10
14秒前
我住隔壁我姓王完成签到,获得积分10
15秒前
15秒前
稳重的书双完成签到,获得积分10
16秒前
hmjhj发布了新的文献求助10
16秒前
猪haha发布了新的文献求助10
17秒前
西瓜宝宝发布了新的文献求助10
17秒前
xiaoqi666完成签到 ,获得积分0
18秒前
蕾蕾完成签到,获得积分10
18秒前
0911完成签到,获得积分20
19秒前
蘧蘧发布了新的文献求助10
19秒前
慕青应助乌兰巴托没有海采纳,获得10
19秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Cosmos as Art Object: Studies in Plato's Timaeus and Other Dialogues 500
What is the Future of Psychotherapy in Digital Age? Technology, AI Bots, and Psychotherapy after Covid 444
Management and the Arts 310
Teaching Social and Emotional Learning in Physical Education 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7634978
求助须知:如何正确求助?哪些是违规求助? 9208984
关于积分的说明 19750549
捐赠科研通 7202906
什么是DOI,文献DOI怎么找? 3275138
关于科研通互助平台的介绍 2436999
邀请新用户注册赠送积分活动 2272068