期刊文献+

家兔半膜肌各亚部肌球蛋白重链表达差异的实验研究 被引量:3

Experimental studies on the differential expression of myosin heavy chain mRNA of various compartments of semimembranosus in rabbit
下载PDF
导出
摘要 目的利用家兔半膜肌各亚部肌纤维类型的分布特征,观察骨骼肌两型肌纤维肌球蛋白重链(MHC)的构成特点,为进一步探讨两型肌纤维的区别以及两型肌纤维转化机制奠定基础。方法取成年家兔半膜肌,通过改良肌球蛋白ATP酶染色法观察半膜肌四个亚部肌纤维类型的构成,应用RT-PCR方法检测各亚部4种MHC亚型mRNA的表达情况。结果固有半膜肌只含有慢肌(Ⅰ型)肌纤维,表达MHCⅠ型和少量MHCⅡa型基因。副半膜肌腹侧亚部除含有少量Ⅰ型肌纤维外,主要含有快肌(Ⅱ型)肌纤维,表达少量MHCⅠ型基因以及MHCⅡa、MHCⅡb和MHCⅡx型基因等四种类型;而副半膜肌背侧和外侧亚部只含有Ⅱ型肌纤维,仅表达MHCⅡa、MHCⅡb和MHCⅡx型基因。结论家兔半膜肌各亚部肌纤维类型几乎均呈单一类型分布。固有半膜肌亚部主要表达MHCⅠ型基因;副半膜肌各亚部主要表达MHCⅡa、MHCⅡb和MHCⅡx型基因,以MHCⅡx型基因为主,各亚部之间存在细微差别。 Objective The feature of the rabbit semimembranosus is that its various compartments only possess one muscle fiber type: slow muscle fiber(typeⅠ) or fast muscle fibers(typeⅡ).To explore differences of the two types of skeletal muscle fiber,the expression of various myosin heavy chains(MHC) isoforms was observe in four compartments of the rabbit semimembranosus.Methods The rabbit semimembranosus was obtained from 10 adult rabbits.The composition of skeletal muscle fiber type was observed in four compartments of the rabbit semimembranosus by myosin ATPase staining method and the expression of various myosin heavy chain(MHC) isoforms was observe by RT-PCR.Results The inherent semimembranosus only contained slow muscle fiber(typeⅠ) and expressed MHCⅠand MHCⅡ a.The ventral compartment of semimembranosus mainly contained fast muscle fibers(typeⅡ)and a little slow muscle fiber(typeⅠ) and expressed MHCⅡa.MHCⅡb and Ⅱx and a few MHCⅠ.while its dorsal and lateral compartment only contained fast muscle and only expressed MHCⅡ a,MHCⅡ b and MHCⅡ x.Conclusion Various compartments of the rabbit semimembranosus almost possessed one muscle fiber type and accordingly expressed various myosin heavy chain(MHC) isoforms.
出处 《遵义医学院学报》 2011年第5期448-452,共5页 Journal of Zunyi Medical University
基金 遵义医学院博士启动基金项目(NO:F-132)
关键词 肌球蛋白 半膜肌 肌球蛋白重链(MHC) myosin semimembranosus myosin heavy chain(MHC)
  • 相关文献

参考文献9

  • 1G McKoy, ME Leger, F Bacou, and G Goldspink. Dif- ferential expression of myosin heavy chain mRNA and protein isoforms in four functionally diverse rabbit skeletal muscles during pre- and postnatal development [J].Dev Dyn Mar,1998,211(3): 193-203.
  • 2Brooke MH ~ Kaiser KK.Tbree"myosin adenosine triphosphatase"systems. The nature of their PH lability and sulfhydral dependence. [J]. Histochem Cytochem, 1970, 18(9): 670-672.
  • 3Guth L, Samaha F J. Procedure for the histochemical demonstration of actomyosin ATPase[J]. Exp Neurol,1970,28(2):365-367.
  • 4蔡永清 李明扬 靳仕信.家兔半腱肌和半膜肌的亚部化及肌纤维型构成的研究.大连医学院学报,1988,10(2):45-49.
  • 5Wilborn CD,Willoughby DS. The role of dietary protein intake and resistance training on Myosin heavy chain expression[J]. Int Soc Sprots Nutr, 2004, 1 ( 2 ): 27-34.
  • 6Edwards JG, Bahl J J, Flink IL, et al. Thyrodi hormone influences betamyos in heavy chain (beta MHC) expression[J]. Biochem Biophys Res Comrnun, 1994, 199(3) : 1482-1488.
  • 7Schiaffino S, Reggiani C. Molecular diversity of myofibrillar proteins: gene regulation and functional significance[J].Physiol Rev, 1996,76:371-423.
  • 8Soussi-Yanicostas N,Whalen RG, Petit C. Five skeletal myosin heavy chain genes are organized as a multigene complex in the human genome[J]. Hum Mol Genet, 1993,2:563-569.
  • 9Staron RS Johnson E Mini review. Myosin polymorphism and differential expression in adult human skeletal muscle[J]. Comp Biochem,Physiol, 1993,106B :463-475.

同被引文献42

  • 1朱道立,陈佩林,王康乐,葛娟,别林.小鼠快、慢肌卫星细胞的分离培养及β肌动蛋白的表达[J].上海交通大学学报(医学版),2011,31(1):26-30. 被引量:1
  • 2Lu H, Huang D, Ransohoff RM,et al. Acute skeletalmuscle injury: CCL2 expression by both monocytesand injured muscle is required for repair.FASEB J.2011;25(10):3344-3355.
  • 3Chien SH, Chen SK, Lin SY,et al. Repair method andhealing of skeletal muscle injury. Gaoxiong Yi Xue KeXue Za Zhi.1991;7(9):481-488.
  • 4Mu X,Peng H, Pan H, et al. Study of muscle celldedifferentiation after skeletal muscle injury of micewith a Cre-Lox system.PLoS 0ne.2011 ;6(2):e16699.
  • 5Castiglioni A,Coma G,Rigamonti E,et al.Rovere-Querini P.FOXP3+ T Cells Recruited to Sites of SterileSkeletal Muscle Injury Regulate the Fate of SatelliteCelts and Guide Effective Tissue Regeneration.PLoS0ne.2015;10(6):e0128094.
  • 6Nicholas J, Voss JG, Tsuji J,et al.Time course ofchemokine expression and leukocyte infiltration afteracute skeletal muscle injury in mice.lnnate Immun.2015 Apr;21 (3):266-274.
  • 7Radi ZA, Koza-Taylor PH, Bell RR,et al. Increasedserum enzyme levels associated with kupffer cellreduction with no signs of hepatic or skeletal muscleinjury.Am J Pathol. 2011;179(1):240-247.
  • 8de Almeida P, Tomazoni SS, Frigo L,et al.What is thebest treatment to decrease pro-inflammatory cytokinerelease in acute skeletal muscle injury induced bytrauma in rats: low-level laser therapy, diclofenac, orcryotherapy? Lasers Med Sci.2014:29(2):653-658.
  • 9Wirsdorfer F, Bangen JM, Pastille E,et al. Breaking theco-operation between bystander T-cells and naturalkiller cells prevents the development ofimmunosuppression after traumatic skeletal muscleinjury in mice.Clin Sci (Lond). 2015;128(11):825-838.
  • 10Gumucio JP, Flood MD, Phan AC,et al.Targetedinhibition of TGF-(3 results in an initial improvement butlong-term deficit in force production aftercontraction-induced skeletal muscle injury. JAppIPhysiol (1985). 2013 Aug 15; 115(4):539-45.

引证文献3

二级引证文献7

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部