微循环学杂志
微循環學雜誌
미순배학잡지
CHINESE JOURNAL OF MICROCIRCULATION
2015年
1期
23-25
,共3页
邵珺%孙尉%姚勇%王如心
邵珺%孫尉%姚勇%王如心
소군%손위%요용%왕여심
视网膜动脉平滑肌细胞%分离消化%大鼠
視網膜動脈平滑肌細胞%分離消化%大鼠
시망막동맥평활기세포%분리소화%대서
Retinal microartery smooth muscle cells%Separation%Rats
目的::探讨分离、消化 SD 大鼠视网膜微动脉平滑肌细胞(RMASMCs)的方法。方法:取正常 SD 大鼠眼球,分离视网膜微动脉,利用不同消化酶消化不同时间后,分离 RMASMCs,在倒置显微镜下观察 RMASMCs 形态,并行免疫组化法鉴定。结果:解剖显微镜下成功急性分离视网膜动脉分支,即视网膜微动脉(直径40.23±5.61μm)。1、2、3号消化酶各消化10-16min,RMASMCs 数量逐步增多,16min 时最多(13.4±1.3个/低倍视野),与其它消化时间相比,差异有统计学意义(P <0.05)。倒置显微镜下观察收获的 RMASMCs 呈长梭形、细胞膜完整、边缘光滑;免疫组化染色鉴定其胞浆呈α-action 阳性表达。结论:采用急性分离、逐步消化的方法能成功获取较多数量和较高质量的 RMASMCs。
目的::探討分離、消化 SD 大鼠視網膜微動脈平滑肌細胞(RMASMCs)的方法。方法:取正常 SD 大鼠眼毬,分離視網膜微動脈,利用不同消化酶消化不同時間後,分離 RMASMCs,在倒置顯微鏡下觀察 RMASMCs 形態,併行免疫組化法鑒定。結果:解剖顯微鏡下成功急性分離視網膜動脈分支,即視網膜微動脈(直徑40.23±5.61μm)。1、2、3號消化酶各消化10-16min,RMASMCs 數量逐步增多,16min 時最多(13.4±1.3箇/低倍視野),與其它消化時間相比,差異有統計學意義(P <0.05)。倒置顯微鏡下觀察收穫的 RMASMCs 呈長梭形、細胞膜完整、邊緣光滑;免疫組化染色鑒定其胞漿呈α-action 暘性錶達。結論:採用急性分離、逐步消化的方法能成功穫取較多數量和較高質量的 RMASMCs。
목적::탐토분리、소화 SD 대서시망막미동맥평활기세포(RMASMCs)적방법。방법:취정상 SD 대서안구,분리시망막미동맥,이용불동소화매소화불동시간후,분리 RMASMCs,재도치현미경하관찰 RMASMCs 형태,병행면역조화법감정。결과:해부현미경하성공급성분리시망막동맥분지,즉시망막미동맥(직경40.23±5.61μm)。1、2、3호소화매각소화10-16min,RMASMCs 수량축보증다,16min 시최다(13.4±1.3개/저배시야),여기타소화시간상비,차이유통계학의의(P <0.05)。도치현미경하관찰수획적 RMASMCs 정장사형、세포막완정、변연광활;면역조화염색감정기포장정α-action 양성표체。결론:채용급성분리、축보소화적방법능성공획취교다수량화교고질량적 RMASMCs。
Objective:To investigate the isolated and digest approach of retinal microartery smooth muscle cells (RMASMCs)of SD rats.Method:SD rats were sacrificed after taking the eyes,using different digestive en-zymes to digest different times,separate retinal microartery.RMASMCs morphology was observed under an inverted microscope and identified by immunohistochemical staining.Results:Acute dissecting microscope successfully sepa-rate branch retinal artery that retinal arteriolar diameter was 40.23±5.61μm.No.1,2,3 digestive enzymes to digest each 10 to 1 6 minutes,RMASMCs gradually increased,to 1 6 min when the largest number of smooth muscle cells, was 13.40±1.30/low magnification,compared with other digestion time,the difference was statistically significant (P <0.05).Cells were observed under an inverted microscope RMASMCs typical fusiform smooth muscle cell mem-brane integrity,smooth edges;its showedα-action positive expression by immunohistochemical staining.Conclusion:Acute phase separation and digestion method can successfully obtain larger quantities and higher quality RMASMCs.