• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

血清和黄体中 APN 的表达:黄体甾体生成作用的调节可能依赖于山羊的 AdipoR2/AMPK 通路。

APN Expression in Serum and Corpus Luteum: Regulation of Luteal Steroidogenesis Is Possibly Dependent on the AdipoR2/AMPK Pathway in Goats.

机构信息

College of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.

出版信息

Cells. 2023 May 15;12(10):1393. doi: 10.3390/cells12101393.

DOI:10.3390/cells12101393
PMID:37408227
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10217118/
Abstract

Adiponectin (APN) is an essential adipokine for a variety of reproductive processes. To investigate the role of APN in goat corpora lutea (CLs), CLs and sera from different luteal phases were collected for analysis. The results showed that the APN structure and content had no significant divergence in different luteal phases both in CLs and sera; however, high molecular weight APN was dominant in serum, while low molecular weight APN was more present in CLs. The luteal expression of both AdipoR1/2 and T-cadherin (T-Ca) increased on D11 and 17. APN and its receptors (AdipoR1/2 and T-Ca) were mainly expressed in goat luteal steroidogenic cells. The steroidogenesis and APN structure in pregnant CLs had a similar model as in the mid-cycle CLs. To further explore the effects and mechanisms of APN in CLs, steroidogenic cells from pregnant CLs were isolated to detect the AMPK-mediated pathway by the activation of APN (AdipoRon) and knockdown of APN receptors. The results revealed that P-AMPK in goat luteal cells increased after incubation with APN (1 μg/mL) or AdipoRon (25 μM) for 1 h, and progesterone (P4) and steroidogenic proteins levels (STAR/CYP11A1/HSD3B) decreased after 24 h. APN did not affect the steroidogenic protein expression when cells were pretreated with Compound C or SiAMPK. APN increased P-AMPK and reduced the CYP11A1 expression and P4 levels when cells were pretreated with SiAdipoR1 or SiT-Ca, while APN failed to affect P-AMPK, the CYP11A1 expression or the P4 levels when pretreated with SiAdipoR2. Therefore, the different structural forms of APN in CLs and sera may possess distinct functions; APN might regulate luteal steroidogenesis through AdipoR2 which is most likely dependent on AMPK.

摘要

脂联素(APN)是多种生殖过程中必不可少的脂肪细胞因子。为了研究 APN 在山羊黄体(CL)中的作用,收集了不同黄体期的 CL 和血清进行分析。结果表明,CL 和血清中不同黄体期的 APN 结构和含量没有明显差异;然而,高分子量 APN 在血清中占优势,而低分子量 APN 在 CL 中更为常见。AdipoR1/2 和 T-钙黏蛋白(T-Ca)在 D11 和 17 时黄体表达增加。APN 及其受体(AdipoR1/2 和 T-Ca)主要在山羊黄体甾体生成细胞中表达。妊娠 CL 中的甾体生成和 APN 结构与中期 CL 中的相似。为了进一步探讨 APN 在 CL 中的作用和机制,从妊娠 CL 中分离出甾体生成细胞,通过 APN(AdipoRon)的激活和 APN 受体的敲低来检测 AMPK 介导的途径。结果表明,在孵育 1 小时后,山羊黄体细胞中的 P-AMPK 在加入 APN(1 μg/mL)或 AdipoRon(25 μM)后增加,而在 24 小时后,孕酮(P4)和甾体生成蛋白水平(STAR/CYP11A1/HSD3B)降低。当细胞用 Compound C 或 SiAMPK 预处理时,APN 不影响甾体生成蛋白的表达。当细胞用 SiAdipoR1 或 SiT-Ca 预处理时,APN 增加 P-AMPK,降低 CYP11A1 表达和 P4 水平,而当用 SiAdipoR2 预处理时,APN 不能影响 P-AMPK、CYP11A1 表达或 P4 水平。因此,CL 和血清中 APN 的不同结构形式可能具有不同的功能;APN 可能通过 AdipoR2 调节黄体甾体生成,而 AdipoR2 可能依赖于 AMPK。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f052/10217118/03ac9629e4f3/cells-12-01393-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f052/10217118/5aa38f917e4a/cells-12-01393-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f052/10217118/6f5a219e00bd/cells-12-01393-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f052/10217118/1f488d1ed14f/cells-12-01393-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f052/10217118/b6914cce9216/cells-12-01393-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f052/10217118/06da37adbe02/cells-12-01393-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f052/10217118/9408c2f66ce3/cells-12-01393-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f052/10217118/599f145ca97f/cells-12-01393-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f052/10217118/03ac9629e4f3/cells-12-01393-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f052/10217118/5aa38f917e4a/cells-12-01393-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f052/10217118/6f5a219e00bd/cells-12-01393-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f052/10217118/1f488d1ed14f/cells-12-01393-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f052/10217118/b6914cce9216/cells-12-01393-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f052/10217118/06da37adbe02/cells-12-01393-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f052/10217118/9408c2f66ce3/cells-12-01393-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f052/10217118/599f145ca97f/cells-12-01393-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f052/10217118/03ac9629e4f3/cells-12-01393-g008.jpg

相似文献

1
APN Expression in Serum and Corpus Luteum: Regulation of Luteal Steroidogenesis Is Possibly Dependent on the AdipoR2/AMPK Pathway in Goats.血清和黄体中 APN 的表达:黄体甾体生成作用的调节可能依赖于山羊的 AdipoR2/AMPK 通路。
Cells. 2023 May 15;12(10):1393. doi: 10.3390/cells12101393.
2
Autophagic and apoptotic proteins in goat corpus luteum and the effect of Adiponectin/AdipoRon on luteal cell autophagy and apoptosis.羊黄体中自噬和凋亡蛋白及脂联素/脂联素受体对黄体细胞自噬和凋亡的影响。
Theriogenology. 2024 Jan 15;214:245-256. doi: 10.1016/j.theriogenology.2023.11.001. Epub 2023 Nov 3.
3
Abundance of adiponectin mRNA transcript in the buffalo corpus luteum during the estrous cycle and effects on progesterone secretion in vitro.在发情周期中水牛黄体中脂联素 mRNA 转录本的丰度及其对体外孕激素分泌的影响。
Anim Reprod Sci. 2019 Sep;208:106110. doi: 10.1016/j.anireprosci.2019.106110. Epub 2019 Jun 26.
4
Luteal P4 synthesis in early pregnant gilts after induction of estrus with PMSG/hCG.用孕马血清促性腺激素/人绒毛膜促性腺激素诱导发情后,早期妊娠后备母猪的黄体孕酮合成。
Anim Reprod Sci. 2016 Mar;166:28-35. doi: 10.1016/j.anireprosci.2016.01.001. Epub 2016 Jan 6.
5
Relationships between size, steroidogenesis and miRNA expression of the bovine corpus luteum.牛黄体的大小、类固醇生成和 miRNA 表达之间的关系。
Theriogenology. 2020 Mar 15;145:226-230. doi: 10.1016/j.theriogenology.2019.10.033. Epub 2019 Oct 31.
6
PKA and AMPK Signaling Pathways Differentially Regulate Luteal Steroidogenesis.PKA 和 AMPK 信号通路对黄体甾体生成作用的调控存在差异。
Endocrinology. 2021 Apr 1;162(4). doi: 10.1210/endocr/bqab015.
7
Effect of oestrus synchronization with PGF2α/eCG/hCG on luteal P4 synthesis in early pregnant gilts.前列腺素F2α/孕马血清促性腺激素/人绒毛膜促性腺激素同期发情对早期妊娠后备母猪黄体孕酮合成的影响。
Reprod Domest Anim. 2014 Dec;49(6):1034-42. doi: 10.1111/rda.12433. Epub 2014 Oct 8.
8
Melatonin promotes progesterone secretion in sheep luteal cells by regulating autophagy via the AMPK/mTOR pathway.褪黑素通过 AMPK/mTOR 通路调控自噬促进绵羊黄体细胞分泌孕酮。
Theriogenology. 2024 Jan 15;214:342-351. doi: 10.1016/j.theriogenology.2023.11.010. Epub 2023 Nov 13.
9
NR4A1-mediated regulation of lipid droplets in progesterone synthesis in goat luteal cells†.NR4A1 介导调控脂滴在山羊黄体细胞孕激素合成中的作用。
Biol Reprod. 2024 Sep 14;111(3):640-654. doi: 10.1093/biolre/ioae085.
10
Corpora lutea of pregnant and pseudopregnant domestic cats reveal similar steroidogenic capacities during the luteal life span.怀孕和假孕家猫的黄体在黄体期显示出相似的类固醇生成能力。
J Steroid Biochem Mol Biol. 2014 Oct;144 Pt B:373-81. doi: 10.1016/j.jsbmb.2014.08.010. Epub 2014 Aug 17.

本文引用的文献

1
Soluble T-cadherin promotes pancreatic β-cell proliferation by upregulating Notch signaling.可溶性T-钙黏蛋白通过上调Notch信号促进胰腺β细胞增殖。
iScience. 2022 Nov 7;25(11):105404. doi: 10.1016/j.isci.2022.105404. eCollection 2022 Nov 18.
2
Adiponectin affects uterine steroidogenesis during early pregnancy and the oestrous cycle: An in vitro study.脂联素对早孕和发情周期子宫甾体生成的影响:一项体外研究。
Anim Reprod Sci. 2022 Oct;245:107067. doi: 10.1016/j.anireprosci.2022.107067. Epub 2022 Sep 6.
3
IL11 stimulates ERK/P90RSK to inhibit LKB1/AMPK and activate mTOR initiating a mesenchymal program in stromal, epithelial, and cancer cells.
白细胞介素11刺激细胞外信号调节激酶/90kDa核糖体S6激酶抑制肝脏激酶B1/AMP活化蛋白激酶并激活雷帕霉素靶蛋白,从而在基质细胞、上皮细胞和癌细胞中启动间充质程序。
iScience. 2022 Jul 20;25(8):104806. doi: 10.1016/j.isci.2022.104806. eCollection 2022 Aug 19.
4
Phosphoproteomics reveals that camel and goat milk improve glucose homeostasis in HDF/STZ-induced diabetic rats through activation of hepatic AMPK and GSK3-GYS axis.磷酸化蛋白质组学揭示,骆驼奶和羊奶通过激活肝 AMPK 和 GSK3-GYS 轴改善 HDF/STZ 诱导的糖尿病大鼠的葡萄糖稳态。
Food Res Int. 2022 Jul;157:111254. doi: 10.1016/j.foodres.2022.111254. Epub 2022 Apr 16.
5
Expression pattern and cellular localization of two critical non-nuclear progesterone receptors in the ovine corpus luteum during the estrous cycle and early pregnancy.在绵羊发情周期和早期妊娠期间,两个关键的非核孕激素受体在黄体中的表达模式和细胞定位。
Anim Reprod Sci. 2022 Aug;243:107026. doi: 10.1016/j.anireprosci.2022.107026. Epub 2022 Jun 15.
6
Expression patterns of genes in steroidogenic, cholesterol uptake, and liver x receptor-mediated cholesterol efflux pathway regulating cholesterol homeostasis in natural and PGF2α induced luteolysis as well as early pregnancy in ovine corpus luteum.类固醇生成、胆固醇摄取以及肝 X 受体介导的胆固醇外排途径中基因的表达模式在绵羊黄体自然和 PGF2α 诱导的黄体溶解以及早期妊娠中的胆固醇动态平衡调节。
Anim Reprod Sci. 2022 May;240:106988. doi: 10.1016/j.anireprosci.2022.106988. Epub 2022 May 5.
7
FSH mediates estradiol synthesis in hypoxic granulosa cells by activating glycolytic metabolism through the HIF-1α-AMPK-GLUT1 signaling pathway.促卵泡生成素通过缺氧诱导因子-1α-腺苷酸活化蛋白激酶-葡萄糖转运蛋白1信号通路激活糖酵解代谢,从而介导缺氧颗粒细胞中的雌二醇合成。
J Biol Chem. 2022 May;298(5):101830. doi: 10.1016/j.jbc.2022.101830. Epub 2022 Mar 15.
8
Gestational exposure to acrylamide suppresses luteal endocrine function through dysregulation of ovarian angiogenesis, oxidative stress and apoptosis in mice.孕期接触丙烯酰胺通过扰乱卵巢血管生成、氧化应激和细胞凋亡而抑制黄体内分泌功能。
Food Chem Toxicol. 2022 Jan;159:112766. doi: 10.1016/j.fct.2021.112766. Epub 2021 Dec 11.
9
Estradiol overcomes adiponectin-resistance in diabetic mice by regulating skeletal muscle adiponectin receptor 1 expression.雌二醇通过调节骨骼肌脂联素受体 1 的表达来克服糖尿病小鼠对脂联素的抵抗。
Mol Cell Endocrinol. 2022 Jan 15;540:111525. doi: 10.1016/j.mce.2021.111525. Epub 2021 Nov 29.
10
The RING-domain E3 ubiquitin ligase RNF146 promotes cardiac hypertrophy by suppressing the LKB1/AMPK signaling pathway.RING 结构域 E3 泛素连接酶 RNF146 通过抑制 LKB1/AMPK 信号通路促进心肌肥厚。
Exp Cell Res. 2022 Jan 1;410(1):112954. doi: 10.1016/j.yexcr.2021.112954. Epub 2021 Nov 29.