Muscles, exercise and obesity: skeletal muscle as a secretory organ

肌动蛋白 医学 骨骼肌 内分泌学 内科学 旁分泌信号 脂肪组织 肌发生 肌生成抑制素 心肌细胞 自分泌信号 安普克 肌肉肥大 生物 细胞生物学 受体 蛋白激酶A 磷酸化
作者
Bente Klarlund Pedersen,Mark A. Febbraio
出处
期刊:Nature Reviews Endocrinology [Springer Nature]
卷期号:8 (8): 457-465 被引量:2312
标识
DOI:10.1038/nrendo.2012.49
摘要

During the past decade, skeletal muscle has been identified as a secretory organ. Accordingly, we have suggested that cytokines and other peptides that are produced, expressed and released by muscle fibres and exert either autocrine, paracrine or endocrine effects should be classified as myokines. The finding that the muscle secretome consists of several hundred secreted peptides provides a conceptual basis and a whole new paradigm for understanding how muscles communicate with other organs, such as adipose tissue, liver, pancreas, bones and brain. However, some myokines exert their effects within the muscle itself. Thus, myostatin, LIF, IL-6 and IL-7 are involved in muscle hypertrophy and myogenesis, whereas BDNF and IL-6 are involved in AMPK-mediated fat oxidation. IL-6 also appears to have systemic effects on the liver, adipose tissue and the immune system, and mediates crosstalk between intestinal L cells and pancreatic islets. Other myokines include the osteogenic factors IGF-1 and FGF-2; FSTL-1, which improves the endothelial function of the vascular system; and the PGC-1α-dependent myokine irisin, which drives brown-fat-like development. Studies in the past few years suggest the existence of yet unidentified factors, secreted from muscle cells, which may influence cancer cell growth and pancreas function. Many proteins produced by skeletal muscle are dependent upon contraction; therefore, physical inactivity probably leads to an altered myokine response, which could provide a potential mechanism for the association between sedentary behaviour and many chronic diseases.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

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
萱1988完成签到,获得积分10
刚刚
Ava应助喜悦香薇采纳,获得60
2秒前
3秒前
5秒前
xuyang完成签到,获得积分10
6秒前
坤坤完成签到,获得积分10
6秒前
星空完成签到,获得积分10
7秒前
慕冰蝶发布了新的文献求助10
7秒前
li1完成签到,获得积分20
8秒前
太阳风暴剑完成签到,获得积分10
9秒前
薄荷味的猫完成签到,获得积分10
9秒前
10秒前
尧九完成签到,获得积分10
10秒前
白衣修身完成签到,获得积分10
10秒前
坦率傲玉完成签到 ,获得积分10
11秒前
漂泊的思绪完成签到,获得积分10
11秒前
东郭谷雪发布了新的文献求助20
11秒前
光亮妙之完成签到,获得积分10
12秒前
Sun_Chen完成签到,获得积分10
12秒前
小二郎应助科研通管家采纳,获得30
12秒前
赘婿应助科研通管家采纳,获得10
12秒前
明亮囧完成签到 ,获得积分10
12秒前
诚心闭月完成签到,获得积分10
13秒前
exosome完成签到,获得积分20
13秒前
BaooooooMao完成签到,获得积分10
13秒前
11完成签到,获得积分10
13秒前
清醒完成签到,获得积分10
14秒前
liniubi发布了新的文献求助10
14秒前
苹果平安完成签到,获得积分10
15秒前
无心完成签到,获得积分10
16秒前
SCI完成签到 ,获得积分10
16秒前
昏睡的笑南完成签到,获得积分10
17秒前
切奇莉亚完成签到,获得积分10
18秒前
yousing发布了新的文献求助10
18秒前
万万应助喜东采纳,获得10
18秒前
东鱼鱼鱼完成签到,获得积分10
18秒前
隐形曼青应助Xiancai采纳,获得10
18秒前
pp完成签到,获得积分10
19秒前
lime完成签到,获得积分10
19秒前
微笑梦旋发布了新的文献求助10
19秒前
高分求助中
Evolution 10000
Sustainability in Tides Chemistry 2800
The Young builders of New china : the visit of the delegation of the WFDY to the Chinese People's Republic 1000
юрские динозавры восточного забайкалья 800
English Wealden Fossils 700
Foreign Policy of the French Second Empire: A Bibliography 500
Chen Hansheng: China’s Last Romantic Revolutionary 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3147003
求助须知:如何正确求助?哪些是违规求助? 2798336
关于积分的说明 7827807
捐赠科研通 2454956
什么是DOI,文献DOI怎么找? 1306492
科研通“疑难数据库(出版商)”最低求助积分说明 627808
版权声明 601565