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胞浆

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The UL51 protein was localized to the perinuclear regions at hour 12 PT,and to the nucleus and cytoplasm at later time.

间接免疫荧光法显示,该基因产物早期聚集于COS-7细胞的近核区域,晚期位于胞浆和胞核中。

The HUVECs retained spindled shaped or cobblestone appearance and positively stained by anti-CD31. DAPI staining showed that 90%of scaffolds surface was reendothelialized and endothelial cells were distributed evently on the surface forming a confluent monolayer.

脱细胞支架细胞成分完全脱去,胞外基质保存完好;分离的细胞培养一周后,细胞呈梭形或多角形,核仁清晰,大小均匀,呈典型的铺路石样;免疫荧光检测可见细胞胞浆内有颗粒状红色阳性信号,说明Ⅷ因子相关抗原染色阳性;膜表面有蓝色阳性信号,说明CD31抗原染色阳性。

Immunofluorescence staining and reverse transcription polymerase chain reaction were used to test the expression of syndecan-1 protein and its mRNA in cultured unstimulated RPE cells.

2在正常RPE细胞,可检测到syndecan一1蛋白和mRNA的表达;第四军医大学硕士学位论文未受刺激的RPE细胞胞膜/胞浆、核仁呈现强的黄绿色荧光;随TNF一。

The tumor cells are large in size, very pleomorphic, and have abundant, vacuolated to dense cytoplasm, and hyperpchromatic nuclei with irregular contours and prominent nucleoli.

瘤细胞个大,多形性明显,浆丰,胞浆从空泡状到致密,核深染,外形不规则,核仁明显。

RESULTS: The passaged MSCs exhibited uniform appearance in fusiform shape, and their growth was slowed down after 9 passages, exhibiting cytoplasm vacuolization and body enlarging.

结果:传代培养的骨髓间充质干细胞形态均一,呈梭形、纺锤形,克隆样生长,培养至9代后生长减慢,并出现胞浆空泡化、胞体变大等老化现象。

Moreover, Smad3 and 4 translocated to nucleus on 1d and 3m.

Smad3和4的表达部位在照射后1d和3m由胞浆向胞核转位。

So the action on lymphatic vessel endothelial cell was mainly by paracrine. In this study the expression of VEGF-C in cervical carcinoma was detected in the plasm of tumor cell, and the color observed was yellow.

本研究通过免疫组化的方法检测宫颈癌组织中的VEGF-C的表达,发现其多位于肿瘤细胞的胞浆及胞膜内,呈棕黄色。

Results: Smad4 , T β R II expressed in the plasm of the cell,while p21wafl expressed in the nuclear of the cell .

结果:Smad4、TβRⅡ在正常组织中表达于胞浆,p21~位于胞核。

HGF expressed in cartilage cell plasm, and showed positive in muscle plasm.

研究结果:组织学结果显示,9周时实验组组织学修复优于对照组;实验组Ⅱ型胶原表达较对照组有增强的趋势;HGF在软骨细胞胞浆表达,且发现肌肉组织的肌浆中有阳性表达。

To further validate the above results, in the second part of our research, we measured 〓 of cultured rabbit basilar artery smooth muscle cells growing on glass coverslips using ratiometric video fluorescence microscopy and the 〓-sensitive dye, fura-2, continuing with the investigation of effects of DIDS and NPPB on 5-HT induced 〓 change in these cells.

为进一步证实上述结果,本文第二部分又采用生物荧光双波长影像分析系统测定单细胞胞浆〓浓度瞬即变化技术,观察了DIDS和NPPB对5-HT引起培养的兔脑椎基底动脉平滑肌细胞胞内〓变化的影响。

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