中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2015年
42期
6798-6802
,共5页
郭庆敏%孟旭霞%田椰%胡迭
郭慶敏%孟旭霞%田椰%鬍迭
곽경민%맹욱하%전야%호질
组织构建%组织工程%促红细胞生成素%晶状体%胚胎发育
組織構建%組織工程%促紅細胞生成素%晶狀體%胚胎髮育
조직구건%조직공정%촉홍세포생성소%정상체%배태발육
背景:有研究发现促红细胞生成素对视网膜胚胎发育具有保护作用,但对晶状体胚胎发育的影响的研究尚少有报道。目的:通过观察不同胚胎发育期Wistar大鼠晶状体组织中促红细胞生成素的表达差异,探讨促红细胞生成素在晶状体胚胎发育过程中的作用和意义。方法:选取清洁级Wistar母鼠孕10 d、孕12 d、孕14 d、孕16 d、孕18 d、孕20 d各5只,每只孕鼠氯胺酮麻醉后剖腹随机取胎鼠2只,分离各组的胚鼠眼球组织,并制作石蜡切片,用免疫组织化学法、实时定量PCR方法检测大鼠晶状体组织中促红细胞生成素蛋白及其促红细胞生成素信使核糖核酸的表达。结果与结论:不同胚胎期晶状体组织中均有促红细胞生成素阳性表达,孕10 d至孕16 d,表达量逐渐升高,孕16 d至孕20 d,表达量逐渐降低,孕16 d时达到峰值,各胚胎期促红细胞生成素表达量采用单因素方差分析,差异有显著性意义。结果说明Wistar大鼠胚胎发育过程中,晶状体中促红细胞生成素呈现由低到高、再由高到低的表达量的变化趋势,其表达规律提示促红细胞生成素可能参与了晶状体的胚胎发育过程并在其中发挥保护和调节作用。
揹景:有研究髮現促紅細胞生成素對視網膜胚胎髮育具有保護作用,但對晶狀體胚胎髮育的影響的研究尚少有報道。目的:通過觀察不同胚胎髮育期Wistar大鼠晶狀體組織中促紅細胞生成素的錶達差異,探討促紅細胞生成素在晶狀體胚胎髮育過程中的作用和意義。方法:選取清潔級Wistar母鼠孕10 d、孕12 d、孕14 d、孕16 d、孕18 d、孕20 d各5隻,每隻孕鼠氯胺酮痳醉後剖腹隨機取胎鼠2隻,分離各組的胚鼠眼毬組織,併製作石蠟切片,用免疫組織化學法、實時定量PCR方法檢測大鼠晶狀體組織中促紅細胞生成素蛋白及其促紅細胞生成素信使覈糖覈痠的錶達。結果與結論:不同胚胎期晶狀體組織中均有促紅細胞生成素暘性錶達,孕10 d至孕16 d,錶達量逐漸升高,孕16 d至孕20 d,錶達量逐漸降低,孕16 d時達到峰值,各胚胎期促紅細胞生成素錶達量採用單因素方差分析,差異有顯著性意義。結果說明Wistar大鼠胚胎髮育過程中,晶狀體中促紅細胞生成素呈現由低到高、再由高到低的錶達量的變化趨勢,其錶達規律提示促紅細胞生成素可能參與瞭晶狀體的胚胎髮育過程併在其中髮揮保護和調節作用。
배경:유연구발현촉홍세포생성소대시망막배태발육구유보호작용,단대정상체배태발육적영향적연구상소유보도。목적:통과관찰불동배태발육기Wistar대서정상체조직중촉홍세포생성소적표체차이,탐토촉홍세포생성소재정상체배태발육과정중적작용화의의。방법:선취청길급Wistar모서잉10 d、잉12 d、잉14 d、잉16 d、잉18 d、잉20 d각5지,매지잉서록알동마취후부복수궤취태서2지,분리각조적배서안구조직,병제작석사절편,용면역조직화학법、실시정량PCR방법검측대서정상체조직중촉홍세포생성소단백급기촉홍세포생성소신사핵당핵산적표체。결과여결론:불동배태기정상체조직중균유촉홍세포생성소양성표체,잉10 d지잉16 d,표체량축점승고,잉16 d지잉20 d,표체량축점강저,잉16 d시체도봉치,각배태기촉홍세포생성소표체량채용단인소방차분석,차이유현저성의의。결과설명Wistar대서배태발육과정중,정상체중촉홍세포생성소정현유저도고、재유고도저적표체량적변화추세,기표체규률제시촉홍세포생성소가능삼여료정상체적배태발육과정병재기중발휘보호화조절작용。
BACKGROUND:Studies have found that erythropoietin has a protective effect on embryonic development of the retina, but there are rare studies concerning the embryonic development of the lens. OBJECTIVE: To observe the difference in erythropoietin expression in the lens from Wistar rats at different embryonic periods and to investigate the effect and significance of erythropoietin in the embryonic development of the lens. METHODS:Clean Wistar rats with pregnancy for 10 days (n=5), 12 days (n=5), 14 days (n=5), 16 days (n=5), 18 days (n=5), 20 days (n=5) were randomly colected and divided into six groups. Every two embryonic ratsof the different 30 pregnant rats were obtained randomly by the caesarean operation under ketamine-induced anesthesia. The eye tissues of al the embryonic rats were isolated and cut into sections. The expression of erythropoietin protein and mRNA in rat lens was detected by immunohistochemistry and reverse t ranscription-PCR, respectively. RESULTS AND CONCLUSION:Erythropoietin was distinctly expressed at the six different embryo stages, and the expression of erythropoietin protein and mRNA gradualy increased from embryonic day 10 to embryonic day 16, and decreased from embryonic day 10 to embryonic day 20. There were significant differences between the six groups. These findings indicate that the expression of embryonic appears in a low to high to low fashion during the embryonic development of Wistar rats, which may be closely associated with the developing procedure of lens.