异细胞的

Those suggest that the two capsules both can control the growth of ectopica endometrium by regularing patients endocrine.At the same time,they both increase the activity of NK cells to reinforce the effect of getting rid of the ectopia endometrium.

这说明桂附胶囊和理气胶囊均能通过调节内分泌而抑制异位内膜的血管形成，从而抑制异位内膜的生长；同时增加NK细胞的活性，以加强对异位内膜组织的清除作用。

It indicated that not only can Spirulina cells grow photoautotrophically and photomixtrotrophically, but also can grow heterotroph ically under some specific conditions. light intensity, light quality, temperature, species and concentration of metals, rare

认为螺旋藻细胞不但能进行光合自养和混合营养生长，而且在某些特定的环境条件下，还能进行异养生长；光照强度、光质、温度、金属元素、稀土元素、盐度、藻体细胞浓度、溶氧水平、维生素、激素和磁场等环境因素对螺旋藻细胞的光合性能和细胞产率都有显著影响。

NF-κB is a kind of important nuclear factors which are relative to lots of cellular activities such as activation of immunocyte, development of T and B lymphocyte, stress reaction, cell apoptosis and so on. NF-κB exists in almost all types of cytoplasm in the unreactive form of heterodimer or homodimer.

核转录因子κB(nuclear transcription factorκB， NF-κB)是一类关键性的核转录因子，通常以同源或异源二聚体非活性形式存在于几乎所有类型细胞的胞质，其与免疫细胞的活化，T，B淋巴细胞的发育，应激性反应，细胞凋亡等多种细胞活动有关。

The heterogenic C57BL/6J splenocytes disappeared at 1 day after transfusion, but the syngeneic BALB/c splenocytes could survive for a long time in the peripheral blood of BALB/c mice. The fluorescence intensity was not decreased in two kinds of splenocytes. The results demonstrated that CFSE-labeling with difference concentration is reliable, stable and convenient for spleen lymphocytes tracing in vivo.

异基因的C57BL/6J脾细胞在输注1 d后就快速消失，而同基因BALB/c脾细胞能够在BALB/c小鼠外周血中长期存在，但是两种细胞荧光强度均未见降低，说明荧光染料CFSE差异浓度标记活细胞进行体内示踪是一种稳定的示踪方法。

The hydroxamic acid compounds can also inhibit histone deacetylase and are suitable for use in selectively inducing terminal differentiation, and arresting cell growth and/or apoptosis of neoplastic cells, thereby inhibiting proliferation of such cells.

所述的异羟肟酸化合物还可以抑制组蛋白脱乙酰基酶并且适合于选择性地诱导终末分化，以及阻止赘生性细胞的细胞生长和/或细胞程序死亡，由此抑制这些细胞的增殖。

Results:(1) CBC possesses a natural trabecular structure. Its components is similar to the mineral of bone.(2) CBC has great cellur biocompatibility. It can promote cell adhesion, proliferation and secretory while needn t modification.(3) In nude mice, the ectopic osteogenesis of MCCAB was obvious which was better than that of CBC alone and the new bone formation increased in pace with time. In the MCCAB, both intramembranous and cartilaginous osteogeneses were seen but the former dominated.(4) When MCCAB was autotransplanted intramuscularly, the osteogenesis was much better than that of negative control groups.(5) The MCCAB can repair autogenous calvaria defects effectively and the effect was much better than that of CBM alone and blank group. Conclusion:(1) CBC possesses good biocompatibility, osteoconduction and porous structure, can be used as scaffold material for constructing of tissue engineering bone.

结果：(1)CBC具有天然的多孔网状结构，最大程度地保持了骨矿的微结构特征，可以作为骨组织工程的支架材料；(2)CBC细胞亲和性好，不需作修饰即能促进成骨细胞的粘附、增殖和分泌活动；(3)MSO/CBC复合人工骨在裸鼠皮下异位成骨作用明显，兼有膜内成骨和软骨内成骨的特点，成骨效果明显优于单纯CBC植入组；(4)MSO/CBC复合人工骨兔自体肌袋异位成骨作用明显，血管化充分，成骨效果明显优于单纯CBC植入组；(5)MSO/CBC复合人工骨修复兔颅骨临界性缺损效果好，明显优于单纯植入CBC组和空白对第四旱区大学硕士学位论文一照组，可以作为骨移植替代材料用于骨缺损畸形修复。

Methods To collect 10 specimen residual ear cartilage of microtia patients about 8-year-old and cultured in vitro, dye with toluidine blue and immunohistochemistry of collagen type II.

结果：残耳软骨细胞在体外培养时随代数增加呈异染陛的糖胺多糖减少，第1、3代Ⅱ型胶原阳性细胞比例约68％～71％，第5代为23％、显著降低；冻存后第3代为65％，与同代数的细胞没有差别，100ng／mi浓度的CDMP-1可以将第4代细胞的阳性比例维持在66％，而且冻存和生长因子不会引起细胞周期的变化。

Nither CDMP-1, nor cryopreservation can effect cell cycle of the chondrocytes.

结果：残耳软骨细胞在体外培养时随代数增加呈异染性的糖胺多糖减少，第1、3代Ⅱ型胶原阳性细胞比例约68％/～71％，第5代为23％、显著降低；冻存后第3代为65％，与同代数的细胞没有差别，100ng/ml浓度的CDMP-1可以将第4代细胞的阳性比例维持在66％，而且冻存和生长因子不会引起细胞周期的变化。

There were five groups in the examination of cellular levelK562 group,K562/A02 group,K562+ADM group,K562/A02+ADM group and K562/A02+TTD+ADM group）.The non-cytotoxicity doses to cell lines K562 and K562/A02 of TTD were got by MTT assay.Using flow cytometry (FCM assay to examine the intracellular ADM concentration.There were three groups in the examination of genic,zymologic and protein levelsK562 group,K562/A02 group and K562/A02+TTD group）.The mRNA expression of MDR was measured by fluorescent quantitative reverse transcriptase polymerase chain reaction(RT-PCR.The expression levels of glutathione-S-transferase and topoisomerase Ⅱ were determined by immunohistochemical technique.

细胞水平检测实验分5组（K562组、K562/A02组、K562+ADM组、K562/A02+ADM组和K562/A02+TTD+ADM组），采用MTT法检测TTD对K562和K562/A02细胞的非细胞毒性剂量，流式细胞术检测细胞内阿霉素的浓度，基因、酶学、蛋白水平检测实验分3组（K562组、K562/A02组和K562/A02+TTD组），采用RT-PCR法检测mdr1 mRNA的表达，免疫细胞化学方法检测谷胱甘肽S转移酶π和拓扑异构酶Ⅱ的表达水平，Western-blotting法检测P-糖蛋白和bcl-2表达。

The cells may be autologous, syngeneic, allogeneic or xenogeneic, as tolerance to foreign cells is created in the patient during reactivation of the thymus.

因为患者在胸腺重新活化过程中产生外来细胞抗性，因而这些细胞可以是自体的、同种同基因的、同种异基因的、或异种异基因的。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。