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1.
Chinese Journal of Plastic Surgery ; (6): 122-126, 2012.
Article in Chinese | WPRIM | ID: wpr-246881

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effect of adipose stromal vascular fraction cells (SVFs) with VEGF on the neovascularization of free fat transplantation.</p><p><b>METHODS</b>SVFs were obtained from subcutaneous fat and labelled with DiI. 0.3 ml autologous fat tissue was mixed with 0.2 ml cells: 1) autologous SVFs with VEGF (Group A); 2) autologous SVFs (Group B); 3) complete DMEM (Group C) And then the mixture was injected randomly under the back skin of 12 nude mice. The transplanted fat tissue in three groups was harvested at 2 months after implantation. Wet weight and diameter of fat grafts was measured. After HE and CD31 staining,blood vessel density, viable adipocytes and fibrous proliferation were observed.</p><p><b>RESULTS</b>Trace of SVFs labeled by DiI in vivo could be detected by fluorescent microscope. The wet weight of fat grafts was (191.90 +/- 9.81) mg in group A, (177.01 +/- 10.50) mg in group B, and (92.05 +/- 8.30) mg in group C (P<0.01). The diameter of fat grafts was (0.49 +/- 0.24) cm in group A, (0.40 +/- 0.26) cm in group B, and (0.32 +/- 0.28) cm in group C (P<0.01). Histological analysis showed the blood vessel density was (14.58 +/- 2.06)/HPL in group A, (11.55 +/- 2.18)/HPL in group B, (7.87 +/- 1.55)/HPL in group C. Compared with group B and group C, group A had more adipose tissue with less fat necrosis and fibrosis and had significantly higher capillary density.</p><p><b>CONCLUSIONS</b>The autologous adipose stromal vascular fraction cells with VEGF could improve the neovascularization of free fat significantly. It indicates a wide clinical application in the future.</p>


Subject(s)
Animals , Mice , Adipocytes , Adipose Tissue , Transplantation , Capillaries , Graft Survival , Mice, Nude , Neovascularization, Physiologic , Physiology , Organ Size , Stromal Cells , Transplantation , Vascular Endothelial Growth Factor A , Therapeutic Uses
2.
National Journal of Andrology ; (12): 40-43, 2010.
Article in Chinese | WPRIM | ID: wpr-252876

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the role of bacteria in the etiology of chronic prostatitis.</p><p><b>METHODS</b>A total of 162 complete prostate specimens were obtained at autopsy from organ donors (aged 20 -38 yr) who died of non-prostatic diseases. Each of the samples from the peripheral zone of the prostate was divided into two parts, one for routine pathological examination and immunohistochemical studies of interleukin (IL)-1beta, tumor necrosis factor-alpha (TNF-alpha) and the nerve growth factor (NGF), and the other for PCR assay to detect the bacterial 16S rRNA gene (16S rDNA).</p><p><b>RESULTS</b>Fifty-one (31.5%) of the total specimens presented pathological changes of chronic prostatitis, of which 44 had mild focal stromal, 5 mild focal stromal and periglandular and 2 mild focal periglandular inflammation. The positive rate of 16S rDNA was 19.1% (31/162), 51.0% (26/51) in the chronic prostatitis and 4.5% (5/111) in the non-prostatitis specimens (chi2 = 29.783, P < 0.01). In the specimens with chronic prostatitis, the expressions of IL-1beta, TNF-alpha and NGF were significantly higher in the 16S rDNA positive than in the 16S rDNA negative group (P < 0.01).</p><p><b>CONCLUSION</b>Bacterial inflammation may play an important role in the etiology of chronic prostatitis.</p>


Subject(s)
Adult , Humans , Male , Young Adult , Chronic Disease , Genes, rRNA , Interleukin-1beta , Metabolism , Nerve Growth Factor , Metabolism , Prostate , Metabolism , Microbiology , Pathology , Prostatitis , Metabolism , Microbiology , Pathology , RNA, Bacterial , Genetics , RNA, Ribosomal , RNA, Ribosomal, 16S , Genetics , Tumor Necrosis Factor-alpha , Metabolism
3.
Chinese Journal of Oncology ; (12): 452-455, 2006.
Article in Chinese | WPRIM | ID: wpr-236918

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the role and significance of FHIT genes depletion, p53 overexpression and HPV16/18 infection in cervical intraepithelial neoplasia (CIN) and cervical carcinoma (CC).</p><p><b>METHODS</b>Tumor samples taken from 52 cases of CIN and 69 cases of CC were processed by immunohistochemistry (SP) to determine the expression of FHIT genes and p53 protein, by in situ hybridization to detect HPV16/18 infection, and were compared with those in 18 cases of normal cervical tissues as control.</p><p><b>RESULTS</b>(1) The FHIT expression was positive in normal cervical tissue with no depletion occurred, and was 30.8% in CIN. It was significantly higher in CIN III and carcinoma groups than that in normal and CIN I/II groups (P < 0.01). The depleted expression of FHIT in infiltrating cervical carcinoma group was 66.7% (46/69), significantly higher than that in normal and CIN groups (P < 0.01). Along with the decreasing of cell differentiation, the negative rate of FHIT raised. (2) The positive expression of p53 in CC group was 56.5% (39/69) and the HPV16/18 was 84.1% (58/69), both higher than that in CIN and normal groups (P < 0.05). (3) In CIN and CC groups, the positive rate of p53 in cases with positive or negative FHIT expression was similar (P > 0.05). (4) There is a negative correlation between FHIT and p53 expression. The rate of HPV16/18 infection in the depleted expression of FHIT group was significantly higher than that in FIHT normal expression group (P < 0.01).</p><p><b>CONCLUSION</b>(1) The FHIT-depletion is related with cervical carcinogenesis. It may be used as a marker to serve mass screening of CIN-high risk subjects and diagnostic indicator for early cervical carcinoma. (2) Depleted expression of FHIT is frequently associated with p53 over-expression in CIN and CC subjects, but there is no direct correlation between them. (3) HPV16/18 infection may probably be the common cause leading to altered FHIT and p53 expression.</p>


Subject(s)
Female , Humans , Acid Anhydride Hydrolases , Metabolism , Carcinoma, Squamous Cell , Metabolism , Virology , Uterine Cervical Dysplasia , Metabolism , Virology , Human papillomavirus 16 , Genetics , Human papillomavirus 18 , Genetics , Immunohistochemistry , In Situ Hybridization , Neoplasm Proteins , Metabolism , Papillomavirus Infections , Metabolism , Virology , Tumor Suppressor Protein p53 , Metabolism , Uterine Cervical Neoplasms , Metabolism , Virology
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