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1.
Chinese Medical Journal ; (24): 1491-1497, 2013.
Article in English | WPRIM | ID: wpr-350482

ABSTRACT

<p><b>BACKGROUND</b>Many studies on periostin have focused on its role in tumors and vascular reconstruction. However, the effect of periostin on stem cell function remains unclear. The aim of this study was to enhance vitality in adipose-derived stem cells (ADSCs), the effect of periostin on the function of ADSCs was observed.</p><p><b>METHODS</b>Human ADSCs (hADSCs) were isolated from human adipose tissue by collagenase I digestion and collected in multi-periods for in vitro culture. CD29, CD34, CD44, CD45 and CD105 were detected by flow cytometry. In addition, directed differentiation of hADSCs was induced using adipogenic, osteogenic and chondrogenic induction mediums. The induced morphological changes were observed using oil red O, Alizarin red and alcian blue staining. Periostin was administered to hADSCs in an acidic environment. The treatments of cells were divided into three groups: a periostin group (P); an acidic control group (A); a normal group (N). Then the resulting cell proliferation and migration were detected using a Cell Counting Kit-8 (CCK-8) and a transwell chamber assay, respectively.</p><p><b>RESULTS</b>The detection rates of CD29, CD44, CD105, CD34 and CD45 were 98.89%, 93.73%, 86.99%, 0.19% and 0.16%. The specific staining of cells was positive after induction culture. The mean absorbance of the cells in group P and A at 12 hours were 16.67% and 22.22% greater than group N, respectively (P < 0.01). The mean absorbance of cells from group P was 20.00% greater than that of group A at 48 hours (P < 0.05). The mean number of migratory cells per visual field in group A was 50.38% lower than that in group N (P < 0.05). The migratory cell number in group P was 119.98% greater than that in group A (P < 0.05).</p><p><b>CONCLUSIONS</b>The acidic environment impacted hADSC proliferation and inhibited cell migration. However, periostin was able to promote the proliferation and migration of hADSCs despite the acidic environment.</p>


Subject(s)
Adult , Female , Humans , Adipose Tissue , Cell Biology , Antigens, Surface , Cell Adhesion Molecules , Pharmacology , Cell Differentiation , Cell Movement , Cell Proliferation , Cells, Cultured , Stem Cells , Physiology
2.
Chinese Journal of Plastic Surgery ; (6): 272-276, 2011.
Article in Chinese | WPRIM | ID: wpr-246940

ABSTRACT

<p><b>OBJECTIVE</b>To explore the different expression of TGF-beta1 and collagen during the healing process of wound infected by Pseudomonas aeruginosa (PAO1).</p><p><b>METHODS</b>24 female Wistar rats were randomly divided into pure wound group (group A) and wound + PAO1 group (group B). The re-epithelial rate, shrinkage rate and neutrophils number on the wounds were observed on the 1st, 3rd, 7th and 10th day after operation. The expression of TGF-beta1 and collage I, Ill was also detected.</p><p><b>RESULTS</b>On the 7th day, the re-epithelial rate in group A was higher than that in group B, while the shrinkage rate in group A was lower than that in group B. The neutrophils number increased to peak on the 1st day in group B, but on the 3rd day in group A. The TGF-beta1 expression increased after operation in both groups, but it decreased in group B on the 3rd day and re-increased after that. The TGF-beta1 expression was significantly different between the two groups on the 7th day (P < 0.05). The expression of collagen I and III decreased during healing. The expression of collagen III in group A was higher on the 3rd day and was lower on the 7th and 10th day than that in group B, showing a significant difference (P < 0.05).</p><p><b>CONCLUSIONS</b>PAO1 infection could delay the expression of TGF-beta1 and collagen I, III on wound, which may interfere the healing process of wound.</p>


Subject(s)
Animals , Female , Rats , Collagen Type I , Metabolism , Collagen Type III , Metabolism , Pseudomonas Infections , Pathology , Pseudomonas aeruginosa , Rats, Wistar , Skin Transplantation , Surgical Wound Infection , Metabolism , Microbiology , Transforming Growth Factor beta1 , Metabolism , Wound Healing
3.
Chinese Journal of Medical Genetics ; (6): 447-451, 2008.
Article in Chinese | WPRIM | ID: wpr-308042

ABSTRACT

<p><b>OBJECTIVE</b>To study the association of the Pro12Ala and C1431T polymorphism of the PPAR gamma2 gene and their haplotypes with obesity and type 2 diabetes in Chinese population.</p><p><b>METHODS</b>PCR-restriction fragment length polymorphism was used to determine the Pro12Ala and C1431T polymorphisms in 207 patients with type 2 diabetes and 101 non-diabetic control subjects.</p><p><b>RESULTS</b>(1) In non-diabetic control population, the Ala allele frequency was 0.064, the T1431 allele frequency was 0.252. Haplotype analysis showed that the Pro12Ala and C1431T polymorphisms were in linkage disequilibrium (Do=0.63, r(2)=0.074), which constituted three major haplotypes Pro-C, Pro-T and Ala-T. (2) There were no significant differences of the distribution frequencies of the Pro12Ala and C1431T polymorphism and their haplotypes between the type 2 diabetes mellitus group and non-diabetic control group (P > 0.05). (3) The Pro12Ala polymorphism was associated with blood pressure and lipidemia in diabetic patients. The Ala allele significantly decreased the diastolic blood pressure of non-obese diabetic patients (P < 0.05), but it did not benefit to the obese diabetic patients for the lipidemia (P < 0.05). The C1431T polymorphism was associated with overweight and obesity in diabetic patients. The T1431 allele frequency in the body mass index > or = 25 layer was significantly higher than that in the body mass index < 25 layer (P < 0.05).</p><p><b>CONCLUSION</b>The Pro12Ala and C1431T polymorphisms of the PPAR gamma2 gene might not be a major etiological factor for type 2 diabetes; the C1431T polymorphism was associated with overweight or obesity in diabetic patients.</p>


Subject(s)
Female , Humans , Male , Middle Aged , Alanine , Genetics , Amino Acid Substitution , Asian People , Genetics , Diabetes Mellitus, Type 2 , Blood , Genetics , Gene Frequency , Genotype , Haplotypes , Obesity , Genetics , PPAR gamma , Genetics , Polymorphism, Genetic , Proline , Genetics , Triglycerides , Blood
4.
Chinese Journal of Plastic Surgery ; (6): 129-130, 2008.
Article in Chinese | WPRIM | ID: wpr-325890

ABSTRACT

<p><b>OBJECTIVE</b>To practice a more atraumatic, physiological and aesthetically valued approach of construction for neovagina.</p><p><b>METHODS</b>Laparoscopically using peritoneum as neovagina lining.</p><p><b>RESULTS</b>From March 2005 to September 2006, this technique was adopted to treat 10 patients whose diagnosis was congenital absence of vagina. The ages of the patients were from 19 to 32. The operation lasted average 2.34 hours. And hospitalization was about 20.5 days. Follow-up ranged from 3 - 12 months. No complication occurred. All of the patients was satisfied with their sexual life.</p><p><b>CONCLUSIONS</b>Laparoscopically assisted neovaginaplasty, in which peritoneum was substituted for vaginal mucous membrane, was a kind of ideal approach of vaginal creation.</p>


Subject(s)
Adult , Female , Humans , Young Adult , Follow-Up Studies , Laparoscopy , Peritoneum , Transplantation , Plastic Surgery Procedures , Methods , Vagina , Congenital Abnormalities , General Surgery
5.
Chinese Journal of Surgery ; (12): 1537-1540, 2005.
Article in Chinese | WPRIM | ID: wpr-306073

ABSTRACT

<p><b>OBJECTIVE</b>To examine the expression of nestin and neurogenin 3 (Ngn3), the markers of pancreatic stem cells, in the human fetal pancreas.</p><p><b>METHODS</b>The human fetal pancreas tissue of 12 and 14 weeks were examined for the expression of nestin and Ngn3 using the techniques of immunofluorescence dye and RT-PCR.</p><p><b>RESULTS</b>Both nestin and Ngn3 expressed widely in 12 and 14 weeks before in human fetal pancreatic tissue. In these positive cells there was no co-expressing insulin or glucagon. There were nestin and Ngn3 co-expressing cells in ducts but not in the islets. The results of RT-PCR also indicated the expression of nestin and Ngn3.</p><p><b>CONCLUSIONS</b>There was no expression of the markers of mature endocrine cells in the nestin and Ngn3 positive cells, and they were the marks of no-differentiation cells in the human fetal pancreatic tissue.</p>


Subject(s)
Humans , Basic Helix-Loop-Helix Transcription Factors , Genetics , Fluoroimmunoassay , In Vitro Techniques , Intermediate Filament Proteins , Genetics , Microscopy, Fluorescence , Nerve Tissue Proteins , Genetics , Nestin , Pancreas , Cell Biology , Embryology , Metabolism , Reverse Transcriptase Polymerase Chain Reaction
6.
Chinese Journal of Plastic Surgery ; (6): 94-97, 2004.
Article in Chinese | WPRIM | ID: wpr-327302

ABSTRACT

<p><b>OBJECTIVE</b>To illustrate the effects of the site and method of liposuction on differentiation of human preadipocytes.</p><p><b>METHODS</b>Forty-two fatty samples were obtained with liposuction, which were then divided into four groups according to operation sites (abdomen, hip or extremity) and the methods (conventional negative-pressure or syringe method). Each sample was treated with collagenase I to release preadipocytes for in vitro culture. Affected by the differentiation-induced agents for 9 days or 28 days, the cultured adipocytes were stained with Nile red and observed under a fluorescent microscope. The differentiation rates were examined with flow cytometric analysis and the quantity of intracytoplasmic lipids was determined with oil red O staining. The results were analyzed with independent samples t-test (Mann-Whitney) using SPSS 10.0.</p><p><b>RESULTS</b>There was no statistical difference in differentiation at the 9th day or 28th day among the preadipocytes obtained from the abdomen, hip or extremity with the negative-pressure method. The preadipocytes from the abdomen differentiated more at the 28th day than the 9th day (P < 0.05), which was not observed in the hip or the extremity. The preadipocytes obtained from the abdomen with the negative-pressure method differentiated more than those with the syringe method (P < 0.05).</p><p><b>CONCLUSION</b>No essential difference was found in preadipocyte differentiation among the liposuction sites, while the abdomen might have some superiority. The negative-pressure method of liposuction is the first option in future research of tissue engineering. The flow cytometric analysis is a convenient way to study preadipocyte differentiation.</p>


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Abdomen , General Surgery , Adipocytes , Cell Biology , Cell Differentiation , Cells, Cultured , Flow Cytometry , Hip , General Surgery , Lipectomy , Methods , Microscopy, Fluorescence , Oxazines
7.
Chinese Journal of Plastic Surgery ; (6): 85-87, 2003.
Article in Chinese | WPRIM | ID: wpr-256475

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate a method to partially remove gastrocnemius for improvement of the contour of the leg.</p><p><b>METHODS</b>Thirteen patients with bulked calf were undergoing the treatment. With a self-designed apparatus, the gastrocnemius was partially removed by placing the device in the muscle through an incision in the popliteal fossa. The follow-ups were carried out for 1-6 months.</p><p><b>RESULTS</b>Thirteen patients were successfully treated by above mentioned technique. The removed amount of muscle was weighted between 11 g and 201 g, averaged 77 g. All of the patients could be able to walk three days after the operation. But, the normal walk had to take 1 month after of the surgery for recovering. The function of the ankle joint was not obviously influenced.</p><p><b>CONCLUSION</b>The above mentioned technique is a safe and effective method for re-contouring the leg.</p>


Subject(s)
Humans , Cosmetic Techniques , Early Ambulation , Leg , General Surgery , Muscle, Skeletal , General Surgery , Time Factors
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