[1]李金菊,邓锦波.钠尿肽受体A(NPR-A)在小鼠角膜和晶状体发育过程中的表达[J].眼科新进展,2018,38(12):1119-1122.[doi:10.13389/j.cnki.rao.2018.0264]
 LI Jin-Ju,DENG Jin-Bo.Expression of natriuretic peptide receptor A in cornea and lens during the development of mouse[J].Recent Advances in Ophthalmology,2018,38(12):1119-1122.[doi:10.13389/j.cnki.rao.2018.0264]
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钠尿肽受体A(NPR-A)在小鼠角膜和晶状体发育过程中的表达/HTML
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《眼科新进展》[ISSN:1003-5141/CN:41-1105/R]

卷:
38卷
期数:
2018年12期
页码:
1119-1122
栏目:
实验研究
出版日期:
2018-12-05

文章信息/Info

Title:
Expression of natriuretic peptide receptor A in cornea and lens during the development of mouse
作者:
李金菊邓锦波
475001 河南省洛阳市,河南省洛阳正骨医院(河南省骨科医院)(李金菊);475000 河南省开封市,河南大学神经生物研究所 (邓锦波)
Author(s):
LI Jin-JuDENG Jin-Bo
Henan Luoyang Zhenggu Hospital (LI Jin-Ju),Luoyang 475001,Henan Province,China;Henan University Institute of Neurobiology (DENG Jin-Bo),Kaifeng 475000,Henan Province,China
关键词:
角膜和晶状体发育钠尿肽受体A免疫组织化学
Keywords:
cornea and lensdevelopmentnatriuretic peptide receptor Aimmunohistochemistry
分类号:
R772
DOI:
10.13389/j.cnki.rao.2018.0264
文献标志码:
A
摘要:
目的 检测钠尿肽受体A(natriuretic peptide receptor A,NPR-A)在不同鼠龄小鼠角膜和晶状体内的表达,探讨其在小鼠眼发育过程中的作用。方法 选用C57BL/6转基因小鼠,收集从 E14到P90小鼠眼球标本120只,采用40 g·L-1多聚甲醛灌注固定后,石蜡包埋切片,采用免疫组织化学方法对NPR-A在角膜和晶状体中的表达进行免疫荧光检测。结果 在E16,NPR-A高表达于角膜上皮细胞中,并持续至成年;其在角膜基质层和内皮细胞的表达也始于E16,而在P14之后,NPR-A表达随鼠龄的增加逐渐减弱。此外,NPR-A在P0小鼠晶状体上皮细胞膜内被检测到,并持续高表达至成年。在E16,由晶状体后壁上皮细胞生成的初级纤维开始高表达NPR-A,但随着鼠龄的增长和纤维结构的改变而逐渐减弱,直到P90消失。结论 NPR-A可能参与了角膜和晶状体生长和发育,并且对维持角膜上皮细胞的增生和修复以及晶状体的通透性具有重要作用。
Abstract:
Objective To investigate the expression of natriuretic peptide receptor A(NPR-A) in the mouse cornea and lens and to understand the NPR-A’s functions during the mouse development.Methods Total 120 cases of E14 to P90 C57BL/6 transgenic mouse eye specimens were collected and fixed by 40 g·L-1 paraformaldehyde and made paraffin embedded slices,Then,immunohistochemistries of NPR-A were carried out.Results At E16,NPR-A was highly expressed in embryonic corneal epithelial cells,and it continued to express until adulthood.However,P14 afterward,its expression in the corneal stroma and endothelium layer was decreased gradually with age increasing.On the other hand,NPR-A could be found in developing lens as well.For instance,at P0,NPR-A began to appear in the frontal epithelium of lens,and continued to express highly until adulthood.NPR-A could also be expressed highly in lens fibroblasts which were developed from posterior epithelium.With development,its expression decreased gradually,and disappeared in lens fibers totally after P90.Conclusion NPR-A may be involved in the development of cornea and lens.It plays an important role in corneal epithelial cell proliferation and lens repair.On the other hand,the transparency of lens probably is regulated by NPR-A as well.

参考文献/References:

[1] POTTER L R,YODER A R,FLORA D R,ANTOS L K,DICKEY D M.Natriuretic peptiods:their structures,receptors,physiologic functions and therapeutic applications[J].Handb Exp Pharmacol,2009,(191):341-366.
[2] DREWET J G,GARBERS D L.The family of guanylyl cyclase receptors and their ligands[J].Endocr Rev,1994,15(2):135-162.
[3] STONE R A,GLEMBOTSKI C C.Immunoactive natriuretic peptide in the rat eye:molecular forms in anterior uvea and retina[J].Biochem Biophys Res Commun,1986,134(2):1022-1028.
[4] MA Q Y,ZHANG L B.C-type natriuretic peptide functions as an innate neuroprotectant in neonatal hypoxic ischemic brain injury in mouse via natriuretic peptide receptor2[J].Exp Neurol,2018,12(6):304.
[5] KUTTY R K,FLETCHER R T,CHADER G J,KRISHNA G.Expression of guanylate cyclase-A mRNA in the rat retina:detection using polymerase chain reaction[J].Biochem Biophys Res Commun,2016,182(2):851-857.
[6] VALENTINO B,VALENTINO A,LIPARI L.Atrial natriuretic peptide and vasopressin-presence in the ciliary body of eye in the pig (sus domesticus)[J].J Biol Regul Homeost Agents,2014,28(2):351-355.
[7] ZBROJKIEWICZ M,S ′ LIWI N ′ SKI L.Cyclic guanosine monophosphate in the regulation of the cell function[J].Postepy Hig Med Dosw,2016,70:1276-1285.
[8] CAMMARATA P R,BRAUN B,DIMITRIJEVICH S D.Characterization and functional expression of the natriuretic peptide system in human lens epithelial cells[J].Mol Vis,2016,16(3):630-638.
[9] SATO C,KANEKO H,KONDO T.Association of intraocular pressure changes with right ventricular diameter and brain natriuretic peptide in a case of pulmonary arterial hypertension[J].J Glaucoma,2016,25(3):295-298.
[10] AALTONEN V,KINNUNEN K,JOUHILAHTI E M.Hypoxic conditions stimulate the release of B-type natriuretic peptide from human retinal pigment epithelium cell culture[J].Acta Ophthalmol,2014,92(8):740-744.
[11] BASSNETT S,SHI Y,VRENSEN G F.Biological glass:structural determinants of eye lens transparency[J].Philos Trans R Soc Lond B Biol Sci,2011,366(1568):1250-1264.
[12] LI J J,LI R L,LI X,LIU K,DENG J X,WU P,et al.Expression of natriuretic peptide receptor A in mouse retina development[J].Acta Anatom Sin,2014,45(5):591-598.
李金菊,李瑞玲,李雪,刘恺,邓洁心,吴萍,等.钠尿肽受体A在小鼠视网膜发育过程中的表达[J].解剖学报,2014,45(5):591-598.
[13] CAI Z M,CHEN R H,KANG Z H,CHEN L Y,WU Y Q,ZHU X J,et al.Ultrastructural observation of lens epithelial cells and lens fibers in cataract[J].J Anatom,1995,18(3):219-223.
蔡兆明,陈瑞华,康仲涵,陈莲云,吴翊钦,朱学军,等.白内障晶状体上皮细胞及晶状体纤维超微结构的观察[J].解剖学杂志,1995,18(3):219-223.
[14] AALTONEN V,KINNUNEN K.C-type natriuretic peptide protects the retinal pigment epithelium against advanced glycation end product-induced barrier dysfunction[J].Acta Ophthalmol,2014,92(8):740-744.
[15] TAKEHIKO I,TAISAKU T,KAZUO M.Discovery and in vivo effects of novel human natriuretic peptide receptor A (NPR-A) agonists with improved activity for rat NPR-A[J].Bioorgan Medic Chem,2017,11(6):647-650.
[16] WORMSTONE I M,WRIDE M A.The ocular lens:a classic model for development,physiology and disease[J].Philos Trans R Soc Lond B Biol Sci,2016,66(1568):1190-1192.

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备注/Memo

备注/Memo:
国家自然科学基金面上项目(编号:30670688、30771140、31070952)
更新日期/Last Update: 2018-12-04