1.Nondestructive Assessment of Glycosaminoglycans in Engineered Cartilages Using Hexabrix-Enhanced Micro-Computed Tomography.
Long Hao JIN ; Byung Hyune CHOI ; Young Jick KIM ; Hyun Ju OH ; Byoung Ju KIM ; Xiang Yun YIN ; Byoung Hyun MIN
Tissue Engineering and Regenerative Medicine 2018;15(3):311-319
It is very useful to evaluate the content and 3D distribution of extracellular matrix non-destructively in tissue engineering. This study evaluated the feasibility of using micro-computed tomography (µCT) with Hexabrix to measure quantitatively sulfated glycosaminoglycans (GAGs) of engineered cartilage. Rabbit chondrocytes at passage 2 were used to produce artificial cartilages in polyglycolic acid scaffolds in vitro. Engineered cartilages were incubated with Hexabrix 320 for 20 min and analyzed via µCT scanning. The number of voxels in the 2D and 3D scanning images were counted to estimate the amount of sulfated GAGs. The optimal threshold value for quantification was determined by regression analysis. The 2D µCT images of an engineered cartilage showed positive correlation with the histological image of Safranin-O staining. Quantitative data obtained with the 3D µCT images of 14 engineered cartilages showed strong correlation with sulfated GAGs contents obtained by biochemical analysis (R² = 0.883, p < 0.001). Repeated exposure of engineered cartilages to Hexabrix 320 and µCT scanning did not significantly affect cell viability, total DNA content, or the total content of sulfated GAGs. We conclude that µCT imaging using Hexabrix 320 provides high spatial resolution and sensitivity to assess the content and 3D distribution of sulfated GAGs in engineered cartilages. It is expected to be a valuable tool to evaluate the quality of engineered cartilage for commercial development in the future.
Cartilage*
;
Cell Survival
;
Chondrocytes
;
DNA
;
Extracellular Matrix
;
Glycosaminoglycans*
;
In Vitro Techniques
;
Ioxaglic Acid
;
Polyglycolic Acid
;
Tissue Engineering
2.Repair of Partial Thickness Cartilage Defects Using Cartilage Extracellular Matrix Membrane-Based Chondrocyte Delivery System in Human Ex Vivo Model.
Do Young PARK ; Byoung Hyun MIN ; Hyun Jung LEE ; Young Jick KIM ; Byung Hyune CHOI
Tissue Engineering and Regenerative Medicine 2016;13(2):182-190
Treatment options for partial thickness cartilage defects are limited. The purpose of this study was to evaluate the efficacy of the chondrocyte-seeded cartilage extracellular matrix membrane in repairing partial thickness cartilage defects. First, the potential of the membrane as an effective cell carrier was investigated. Secondly, we have applied the chondrocyte-seeded membrane in an ex vivo, partial thickness defect model to analyze its repair potential. After culture of chondrocytes on the membrane in vitro, cell viability assay, cell seeding yield calculation and cell transfer assay were done. Cell carrying ability of the membrane was also tested by seeding different densities of cells. Partial defects were created on human cartilage tissue explants. Cell-seeded membranes were applied using a modified autologous chondrocyte implantation technique on the defects and implanted subcutaneously in nude mice for 2 and 4 weeks. In vitro data showed cell viability and seeding yield comparable to standard culture dishes. Time dependent cell transfer from the membrane was observed. Membranes supported various densities of cells. Ex vivo data showed hyaline-like cartilage tissue repair, integrated on the defect by 4 weeks. Overall, chondrocyte-seeded cartilage extracellular membranes may be an effective and feasible treatment strategy for the repair of partial thickness cartilage defects.
Animals
;
Cartilage*
;
Cell Survival
;
Chondrocytes*
;
Extracellular Matrix*
;
Humans*
;
In Vitro Techniques
;
Lifting
;
Membranes
;
Mice
;
Mice, Nude
3.Efficacy of Team-Based Financial Incentives for Smoking Cessation in the Workplace.
Chang Dong YEO ; Hea Yeon LEE ; Jick Hwan HA ; Hyeon Hui KANG ; Ji Young KANG ; Sung Kyoung KIM ; Myung Sook KIM ; Hwa Sik MOON ; Sang Haak LEE
Yonsei Medical Journal 2015;56(1):295-299
Worksite smoking cessation programs offer accessibility of the target population, availability of occupational health support, and the potential for peer pressure and peer support. The purpose of this study was to identify the efficacy of the financial incentives given to various teams in the workplace. St. Paul's Hospital's employees were enrolled. Each team of employees consisted of smoking participants and non-smoking fellow workers from the same department. The financial incentive of 50000 won (about $45) was rewarded to the team for each successful participant-not to individual members-after the first week and then after one month. If the smokers in the team remained abstinent for a longer time period, the team was given an incentive of 100000 won for each successful participant after 3 and 6 months. A total 28 smoking participants and 6 teams were enrolled. Self-reported abstinence rates validated by urinary cotinine test at 3, 6, and 12 months after the initial cessation were 61%, 54%, and 50%, respectively. Smokers with high nicotine dependence scores or those who began participation 1 month after enrollment initiation had a lower abstinence rate at 3 months, but not at 6 and 12 months. Participants who succeeded at smoking cessation at 12 months were more likely to be older and have a longer smoking duration history. The financial incentives given to teams could be promising and effective to improve long-term rates of smoking cessation. This approach could use peer pressure and peer support in the workplace over a longer period.
Adult
;
Demography
;
Female
;
Health Promotion/*economics
;
Humans
;
Male
;
*Motivation
;
Program Evaluation/*methods
;
Smoking Cessation/*economics
;
Treatment Outcome
;
*Workplace
4.Endobronchial Relapse of Acute Myeloid Leukemia after Allogeneic Stem Cell Transplantation.
Soo Jin NA ; Hyeon Jung LEE ; Jick Hwan HA ; Seung Joon KIM ; Tae Jung KIM ; Hee Je KIM ; Ji Young KANG
Korean Journal of Medicine 2013;85(3):318-323
Myeloid sarcoma is an uncommon extramedullary tumor of immature myeloid cells or myeloblasts. It may occur alone or concurrently with an underlying hematological malignancy. Although it can develop anywhere in the body, common sites include bones, particularly the skull and vertebra, soft tissues, and lymph nodes. However, there have been few reports of myeloid sarcoma occurring in the respiratory system, especially the large airways. We describe a case of endobronchial relapse of acute myeloid leukemia in a patient who achieved complete remission after allogeneic stem cell transplantation. To our knowledge, this is the first such report in Korea.
Granulocyte Precursor Cells
;
Hematologic Neoplasms
;
Humans
;
Korea
;
Leukemia, Myeloid, Acute
;
Lymph Nodes
;
Myeloid Cells
;
Recurrence
;
Respiratory System
;
Sarcoma, Myeloid
;
Skull
;
Spine
;
Stem Cell Transplantation
;
Stem Cells
5.A Case of Mycobacterium kansasii Pulmonary Disease Presenting as Endobronchial Lesions in HIV-Infected Patient.
Moon Sung KIM ; Ji Won HAN ; Su Sin JIN ; Jong Min LEE ; Jick Hwan HAH ; Youn Jeong KIM ; Seung Joon KIM ; Moon Won KANG ; Ji Young KANG
Tuberculosis and Respiratory Diseases 2013;75(4):157-160
Incidence of nontuberculous mycobacterium (NTM) pulmonary disease is increasing with the wider recognition and development of diagnostic technology. Mycobacterium kansasii is the second most common pathogen of NTM pulmonary disease in human immunodeficiency virus (HIV)-infected patients. However in Korea, the incidence of M. kansasii pulmonary disease is relatively low, and there has been no report of M. kansasii pulmonary disease with bronchial involvement in HIV patients, to the best of our knowledge. We report a case of M. kansasii pulmonary disease presenting with endobronchial lesions in an HIV-infected patient complaining of chronic cough with bilateral enlargements of hilar lymph nodes on chest X-ray.
Bronchial Diseases
;
Cough
;
HIV
;
Humans
;
Incidence
;
Korea
;
Lung Diseases*
;
Lymph Nodes
;
Mycobacterium kansasii*
;
Mycobacterium*
;
Nontuberculous Mycobacteria
;
Thorax
6.Successful Rechallenge with Imatinib in a Patient with Chronic Myeloid Leukemia Who Previously Experienced Imatinib Mesylate Induced Pneumonitis.
Seong Woo GO ; Boo Kyeong KIM ; Sung Hak LEE ; Tae Jung KIM ; Joo Yeon HUH ; Jong Min LEE ; Jick Hwan HAH ; Dong Whi KIM ; Min Jung CHO ; Tae Wan KIM ; Ji Young KANG
Tuberculosis and Respiratory Diseases 2013;75(6):256-259
Imatinib mesylate is a targeted therapy that acts by inhibiting tyrosine kinase of the bcr-abl fusion oncoprotein, which is specific to chronic myeloid leukemia (CML), and the c-transmembrane receptor, which is specific to gastrointestinal stromal tumors. Interstitial pneumonitis is a rare adverse event of imatinib therapy. It is clinically difficult to distinguish from infectious pneumonia, which can frequently occur due to the underlying disease. The standard treatment for imatinib-induced pneumonitis is to discontinue the medication and optionally administer corticosteroids. However, there are a few cases of successful retrial with imatinib. We describe a case of successful rechallenge of imatinib in a patient with imatinib-induced interstitial pneumonitis and CML without a recurrence of the underlying disease after 3 months of follow-up.
Adrenal Cortex Hormones
;
Follow-Up Studies
;
Gastrointestinal Stromal Tumors
;
Humans
;
Leukemia, Myelogenous, Chronic, BCR-ABL Positive*
;
Lung Diseases, Interstitial
;
Mesylates*
;
Pneumonia*
;
Protein-Tyrosine Kinases
;
Recurrence
;
Imatinib Mesylate
7.Cartilage Repair Using Mesenchymal Stem Cells.
Byoung Hyun MIN ; Hyun Jung LEE ; Young Jick KIM
Journal of the Korean Medical Association 2009;52(11):1077-1089
Articular cartilage defect rarely heals spontaneously due to its avascularity and low cellularity. Even small articular cartilage defects can develop into osteoarthritis, and subsequently, its management has been a major clinical concern. Although there are several treatment options for cartilage defect, no treatment has been established as a gold standard procedure. Bone marrow stimulation techniques which is equivalent to microfracture these days has been adapted as first line treatment, attributed to their technical easiness and minimal invasiveness to patients. However, this procedure has limitation in reproducing hyaline cartilage, so recent cell-based therapies using autologous chondrocytes or mesenchymal stem cells have drawn particular attention. MSCs regardless of its origin have shown significant potential for chondrogenesis. Novel approaches using MSCs as an alternative cell source for patient derived chondrocytes are currently on trial. In this review, stem cells from various origins considered as cell sources and potential application of mesenchymal stem cells to promote cartilage repair will be discussed. While differentiation of stem cell can be well controlled in vitro, it is not easy to predict the course of differentiation when the stem cell is transplanted. Some novel methods using physical stimulation and material based techniques for differentiation control are introduced in this context. Such differentiation control will be beneficial when it is adapted before transplantation. We call it preconditioning.
Bone Marrow
;
Cartilage
;
Cartilage, Articular
;
Chondrocytes
;
Chondrogenesis
;
Humans
;
Hyaline Cartilage
;
Mesenchymal Stromal Cells
;
Osteoarthritis
;
Physical Stimulation
;
Stem Cells
;
Tissue Therapy
;
Transplants
8.A Case of Choledochoduodenal Fistula as a Delayed Complication after Biliary Metallic Stent Placement in Distal Cholangiocarcinoma.
Seol Kyung MOON ; Dae Young CHEUNG ; Ji Hun KIM ; Eun Joo IM ; Jick Hwan HA ; Jin Il KIM ; Soo Heon PARK ; Jae Kwang KIM
The Korean Journal of Gastroenterology 2008;51(5):314-318
Biliary drainage in patients with malignant biliary obstruction relieves jaundice and prevents the development of cholangitis or hepatic failure from biliary obstruction. Therefore, this may result in better quality of life along with survival prolongation. Biliary stent placement is an effective and safe measure for biliary decompression and is preferred than bypass surgery in high risk patients. Entero-biliary perforation-communication is one of the rare complications of biliary stent. We herein report a case of duodeno-biliary perforation-communication in patient with distal cholangiocarcinoma who presented with duodenal ulcer and obstruction, occurring 4 years later from the metallic biliary stent insertion. Patient was managed with a pyloric metal stent and conservative care.
Aged, 80 and over
;
Bile Duct Neoplasms/complications/*diagnosis
;
Bile Ducts, Intrahepatic/pathology
;
Biliary Fistula/*diagnosis/etiology/pathology
;
Cholangiocarcinoma/complications/*diagnosis
;
Duodenal Diseases/*diagnosis/etiology/pathology
;
Female
;
Humans
;
Intestinal Fistula/*diagnosis/etiology/pathology
;
Stents/*adverse effects
;
Tomography, X-Ray Computed
9.The Change of Cyclooxygenase-2 and Inducible Nitric Oxide Synthase in the Gastric Mucosa One Year after Eradication of Helicobacter pylori.
Sung Soo KIM ; Young Jick SUNG ; Min Kyoung PARK ; Chang Hoon LIM ; Hong Jun YANG ; Tae Ho KIM ; Chang Whan KIM ; Jin Il KIM ; Sok Won HAN ; In Sik CHUNG
The Korean Journal of Gastroenterology 2008;52(5):286-292
BACKGROUND/AIMS: The cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS), the proteins that have the role in the gastric carcinogenesis, are stimulated by H. pylori infection in the gastric mucosa. The aim of this study was to evaluate the expression of COX-2 and iNOS proteins one year after the eradication of H. pylori. METHODS: Gastric antral mucosa from fifty eight patients with chronic gastritis who were all infected with H. pylori was examined for the expression of COX-2 and iNOS proteins before and one year after the eradication of H. pylori by immunohistochemical stain. RESULTS: COX-2 and iNOS proteins were expressed in the epithelial cells and interstitial inflammatory cells of gastric mucosa. Percent expressions of COX-2 and iNOS were significantly decreased one year after the eradication in the patients with cured infection, but not in those having persistent H. pylori. COX-2 and iNOS expressions were well correlated with H. pylori density, acute and chronic inflammation of gastric mucosa. CONCLUSIONS: The eradication of H. pylori can decrease the expression of COX-2 and iNOS in the gastric mucosa in long-term period. This seems to be due to the removal of H. pylori itself and related regression of gastric inflammation.
Cyclooxygenase 2/immunology/*metabolism
;
Drug Therapy, Combination
;
Gastric Mucosa/*enzymology
;
Helicobacter Infections/drug therapy
;
*Helicobacter pylori
;
Humans
;
Nitric Oxide Synthase Type II/immunology/*metabolism
;
Time Factors
10.A Case of Patent Ductus Arteriosus Associated with Pulmonary Valve Endocarditis.
Sang Hee KIM ; Hyun Young WOO ; Jick Hwan HA ; Won Chul KIM ; Youn Suk CHOI ; Dong Hyeon RHEE ; Ji Hoon KIM ; Chul Soo PARK ; Yong Seog OH ; Ho Joong YOUN ; Wook Sung CHUNG ; Soon Jo HONG
Journal of Cardiovascular Ultrasound 2006;14(1):33-35
Isolated infective endocarditis in the native pulmonary valve is unusual in non-intravenous drug user. Intravenous drug abuse, alcoholism, sepsis, catheter related infections and congenital heart diseases account for the majority of predisposing factors. We report a case of patent ductus arteriosus complicating infective endocarditis involving pulmonary valve. A 24-year-old female was admitted with fever of unknown origin Physical examination revealed continuous murmur at left 2nd intercostals space. Transthoracic and transesophageal echocardiography was performed and patent ductus arteriosus and vegetation at the pulmonary valve were noted. Chest CT scan revealed multiple patch infiltrate suggestive of septic emboli. After 4 weeks of antibiotic treatment, she had no clinical signs of fever, and blood culture be negative. Percutaneous trans-catheter closure of patent ductus arteriosus was done after 2 months.
Alcoholism
;
Catheter-Related Infections
;
Causality
;
Drug Users
;
Ductus Arteriosus, Patent*
;
Echocardiography, Transesophageal
;
Endocarditis*
;
Female
;
Fever
;
Fever of Unknown Origin
;
Heart Diseases
;
Humans
;
Physical Examination
;
Pulmonary Valve*
;
Sepsis
;
Substance Abuse, Intravenous
;
Tomography, X-Ray Computed
;
Young Adult

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