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冬眠达乌尔黄鼠的钠钾-ATP 酶、钙-ATP 酶和 SERCA 的显著可塑性有助于抵抗肌肉废用性萎缩。

Remarkable plasticity of Na, K-ATPase, Ca-ATPase and SERCA contributes to muscle disuse atrophy resistance in hibernating Daurian ground squirrels.

机构信息

Key Laboratory of Resource Biology and Biotechnology in Western China (Northwest University), Ministry of Education, Xi'an, 710069, China.

Shaanxi Sci-Tech University, School of Biological Science and Engineering, Hanzhong, 723001, China.

出版信息

Sci Rep. 2017 Sep 5;7(1):10509. doi: 10.1038/s41598-017-10829-6.

DOI:10.1038/s41598-017-10829-6
PMID:28874726
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5585226/
Abstract

We investigated cytosolic calcium (Ca) and sarcoplasmic reticulum Ca regulation in skeletal muscle fibers of hibernating Daurian ground squirrels (Spermophilus dauricus), non-hibernating hindlimb-unloaded (HLU) squirrels, and HLU rats to clarify the molecular mechanisms involved in preventing muscle atrophy in hibernators. The Na, K-ATPase and Ca-ATPase activities in the soleus muscle (SOL) of squirrels were maintained in hibernation, decreased during interbout arousal (IB-A), and increased to autumn/pre-hibernation (AUT/Pre-H) levels in torpor after interbout arousal (Post-IBA), whereas activities in the extensor digitorum longus muscle (EDL) were stable during hibernation, but increased during post-hibernation (Post-H). Activities increased in the SOL of HLU rats, but were stable in HLU squirrels. Sarco/endoplasmic reticulum Ca-ATPase (SERCA) activity in the SOL decreased in IB-A squirrels, but returned to AUT/Pre-H levels in the Post-IBA group; no significant changes were found in the EDL. SERCA activity increased in the EDL of HLU squirrels and SOL of HLU rats. Compared with AUT/Pre-H, SERCA type 2 protein expression increased in the SOL and EDL of IB-A and Post-IBA squirrels, but increased in the SOL only in HLU animals. We also describe the protein kinase A changes in this paper. Thus, hibernating ground squirrels displayed remarkable Na, K-ATPase, Ca-ATPase, and SERCA plasticity.

摘要

我们研究了冬眠达乌尔黄鼠(Spermophilus dauricus)、非冬眠后肢去负荷(hindlimb-unloaded,HLU)松鼠和 HLU 大鼠骨骼肌纤维的细胞质钙(Ca)和肌浆网 Ca 调节,以阐明参与防止冬眠动物肌肉萎缩的分子机制。在冬眠期间,松鼠比目鱼肌(soleus muscle,SOL)中的 Na,K-ATP 酶和 Ca-ATP 酶活性得以维持,在觉醒间隔(interbout arousal,IB-A)期间减少,并在觉醒后间隔(post-interbout arousal,Post-IBA)的蛰伏期间增加到秋季/冬眠前(autumn/pre-hibernation,AUT/Pre-H)水平,而伸趾长肌(extensor digitorum longus muscle,EDL)中的活性在冬眠期间保持稳定,但在冬眠后增加。HLU 大鼠的 SOL 活性增加,而 HLU 松鼠则保持稳定。SOL 中的肌浆/内质网 Ca-ATP 酶(sarco/endoplasmic reticulum Ca-ATPase,SERCA)活性在 IB-A 松鼠中减少,但在 Post-IBA 组中恢复到 AUT/Pre-H 水平;在 EDL 中未发现明显变化。HLU 松鼠的 EDL 和 HLU 大鼠的 SOL 中的 SERCA 活性增加。与 AUT/Pre-H 相比,IB-A 和 Post-IBA 松鼠的 SOL 和 EDL 中 SERCA 类型 2 蛋白表达增加,但仅在 HLU 动物的 SOL 中增加。我们还在本文中描述了蛋白激酶 A 的变化。因此,冬眠达乌尔黄鼠表现出显著的 Na,K-ATP 酶、Ca-ATP 酶和 SERCA 可塑性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557f/5585226/8ae824381016/41598_2017_10829_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557f/5585226/9ef8b66bd72c/41598_2017_10829_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557f/5585226/cc98fe7bdf67/41598_2017_10829_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557f/5585226/14c5747aaece/41598_2017_10829_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557f/5585226/e9bc5036350e/41598_2017_10829_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557f/5585226/0cab76f6cec9/41598_2017_10829_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557f/5585226/f5aaa1da7465/41598_2017_10829_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557f/5585226/570d5f812b83/41598_2017_10829_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557f/5585226/8ae824381016/41598_2017_10829_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557f/5585226/9ef8b66bd72c/41598_2017_10829_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557f/5585226/cc98fe7bdf67/41598_2017_10829_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557f/5585226/14c5747aaece/41598_2017_10829_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557f/5585226/e9bc5036350e/41598_2017_10829_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557f/5585226/0cab76f6cec9/41598_2017_10829_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557f/5585226/f5aaa1da7465/41598_2017_10829_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557f/5585226/570d5f812b83/41598_2017_10829_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557f/5585226/8ae824381016/41598_2017_10829_Fig8_HTML.jpg

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