

版權說明:本文檔由用戶提供并上傳,收益歸屬內容提供方,若內容存在侵權,請進行舉報或認領
文檔簡介
1、Objective The study was focused on the effect and mechanism of IFN-α and IFN-γ on the proliferation and migration of the lymphatic endothelial cell (LEC), and further discovering the safe, effective and practical inhibi
2、tors of lymphangiogenesis.Materials and Methods LECs were taken from the pig thoracic duct. 1. Identification of LEC:LYVE-1 and VEGFR-3 were used to identify LEC. 2. Microscope and electron microscope observation. 3. In
3、hibitory experiment: Two groups, IFN-α and IFN-γ, were designed in the inhibitory experiment. In each group, we adopted two methods to observe the proliferation and migration of LECs which were affected by IFN-α and IFN-
4、γ. (1) Method of scraping line: In IFN-α group and IFN-γ group, control group and 3 experimental groups of different doses were set respectively. (2)MTT: The control group and six experimental groups of different concent
5、ration were set in IFN-αgroup and IFN-γ group, respectively. 4. Apoptotic assay: (1) Caspase staining. (2) Hoechst staining.5. IFN experiment in vivo: Lymphatics of rabbit's two posterior limbs were cut and then IFN-α an
6、d 0.9% NaCl solution were injected around the lymphatic of each limb respectively to observe healing of the lymphatics.Results 1. Identification of LEC: The cultured cells were identified as typical LECs by LYVE-1 andVE
7、GFR-3. 2. LM, SEM and TEM observations: Under LM, LECs presented the typical cha racter of "cobblestone". Under TEM, ultrastructure of LECs, desmosome-like structures and so on were observed. 3. Method of scraping line:
8、When concentration of IFN-α and IFN-γ reached 1000ng/ml, a distinct inhibitive effect can be found (P<0.01). Both could distinctly inhibit the proliferation and migration of LEC. 4. MTT: When the dose of IFN-α and IFN-γ
9、reached 2000ng/ml, both could significantly inhibit the proliferation and migration of LEC (P<0.01). 5. Apoptotic tests: (1) Caspase staining: The positive cells of apoptosis stained brown can be observed. (2) Hoechst st
10、aining: The apoptotic bodies surrounding nucleus of LECs could be observed. 6. IFN experiment in vivo: After 16days of the operation, the lymphatic which was injected with 0.9% NaCl solution healed (no leak of dye) and t
溫馨提示
- 1. 本站所有資源如無特殊說明,都需要本地電腦安裝OFFICE2007和PDF閱讀器。圖紙軟件為CAD,CAXA,PROE,UG,SolidWorks等.壓縮文件請下載最新的WinRAR軟件解壓。
- 2. 本站的文檔不包含任何第三方提供的附件圖紙等,如果需要附件,請聯(lián)系上傳者。文件的所有權益歸上傳用戶所有。
- 3. 本站RAR壓縮包中若帶圖紙,網(wǎng)頁內容里面會有圖紙預覽,若沒有圖紙預覽就沒有圖紙。
- 4. 未經(jīng)權益所有人同意不得將文件中的內容挪作商業(yè)或盈利用途。
- 5. 眾賞文庫僅提供信息存儲空間,僅對用戶上傳內容的表現(xiàn)方式做保護處理,對用戶上傳分享的文檔內容本身不做任何修改或編輯,并不能對任何下載內容負責。
- 6. 下載文件中如有侵權或不適當內容,請與我們聯(lián)系,我們立即糾正。
- 7. 本站不保證下載資源的準確性、安全性和完整性, 同時也不承擔用戶因使用這些下載資源對自己和他人造成任何形式的傷害或損失。
最新文檔
- 血管內皮抑制因子angiostatin和thalidomide對淋巴管內皮細胞生成的影響.pdf
- 血管內皮抑制因子thrombospondin-1對淋巴管內皮細胞生成的影響.pdf
- 血管內皮抑制因子Endostatin和PF-4對淋巴管內皮細胞生成的影響.pdf
- IFN-β和angiostatin分別在離體和在體條件下對淋巴管內皮細胞生成的影響.pdf
- 色素上皮源性因子對淋巴管內皮細胞生成的影響.pdf
- 去甲斑蝥素對淋巴管內皮細胞和淋巴管生成的抑制效應.pdf
- 血管內皮生長因子對血管內皮細胞鎂離子濃度的影響.pdf
- 血管內皮生長因子對血管內皮細胞凋亡的影響及其機理研究.pdf
- 血管內皮生長因子對血管內皮細胞αv整合素表達的影響.pdf
- 外周血淋巴管內皮祖細胞誘導分化以及細胞因子對淋巴管內皮祖細胞趨化和動員的作用.pdf
- 淋巴管內皮細胞體外對食管癌細胞增殖侵襲及體內對淋巴管生成的影響.pdf
- KLF4在創(chuàng)傷新生血管內皮細胞中的表達和對血管內皮細胞功能的影響.pdf
- 腫瘤細胞血管內皮細胞
- 內皮生長因子和炎癥因子環(huán)境下單核細胞向淋巴管內皮細胞誘導分化.pdf
- 腫瘤淋巴管內皮細胞靶向成像的實驗研究.pdf
- 單核細胞向淋巴管內皮細胞的誘導分化.pdf
- 惡性血管內皮細胞瘤
- 重組牛IFn-λ3的制備及其與IFn-α-IFn-β-IFn-γ抗病毒活性比較研究.pdf
- 剪應力和血管內皮生長因子對人骨髓間充質干細胞向血管內皮細胞分化的影響.pdf
- 雞血管內皮鋅指轉錄因子(Vezf1)在血管內皮細胞分化與血管生成中的作用研究.pdf
評論
0/150
提交評論