• 제목/요약/키워드: Avidin

검색결과 121건 처리시간 0.031초

흰쥐에서 하치조신경 절단에 따른 삼차신경절 위성페포에서 GFAP-IR의 변화 (GFAP IMMUNOREACTIVITY IN SATELLITE CEllS OF TRIGEMINAL GANGLION FOllOWING AXOTOMY OF INFERIOR ALVEOLAR NERVE IN RAT)

  • 이창섭;이상호;김흥중
    • 대한소아치과학회지
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    • 제25권1호
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    • pp.249-256
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    • 1998
  • Glial fibrillary acidic proteins (GFAP) are a group of intermediate filaments that are distributed in the cytoplasm of glial cells. GFAP immunoreactivity (GFAP-IR) increase after central and peripheral nerve injuries. The purpose of this study was to determine change of GFAP-IR in rat trigeminal ganglion satellite cells following the axotomy of inferior alveolar nerve(IAN). The immunohistochemistry was carried out using the avidin-biotin-peroxidase complex(ABC) method. 1. Control group : Astrocytes in central root of trigeminal ganglion had strong GFAP-IR, but satellite cells of trigeminal ganglion occasionally had GFAP-IR. The patterns of reactivity in satellite cells of trigeminal ganglion were not concenturated in any specific region of trigeminal ganglion. 2. Three day group after IAN axotomy : There were highly GFAP-IR in satellite cells of trigeminal ganglion in mandibular region. GFAP-IR in maxillary and ophthalmic regions were less intense compared to mandibular region. 3. Seven day group after IAN axotomy : GFAP-IR that were increased compared to control group were seen in the mandibular region. But GFAP-IR were less intense compared to three day group. These results suggest that GFAP-IR increase in specific region of trigeminal ganglion following peripheral axotomy. therefore we suppose that GFAP study offer research tool in trigeminal neuralgia.

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생쥐의 난소의 $\beta$-Endorphin에 대한 면역조직화학적 동정 (Immunohistochemical Identification of $\beta$-Endorphin in the Mouse Ovary)

  • 조사선;이영기;김경진;윤용달;이정주;조완규
    • 한국동물학회지
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    • 제33권2호
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    • pp.152-157
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    • 1990
  • 면역조직화학적 방법을 이용하여 생쥐 난소에서 $\beta$-endorphin이 생성되는 부위를 조사하기 위하여 본 실험을 행하였다. 성숙한 생쥐를 4% neutral buffered paraformaldehyde로 관류고정하였으며 난소를 적출한 후 cryostat로 절편을 만들어 avidin-biotin complex(ABC)를 이용하여 면역색을 하였다. $\beta$-endorphin에 대한 항체반응은 주로 황체에서 일어났으며, theac interna와 theca externa에서는 반응이 나타나지 않았다. 황체에서의 염색 양상은 퇴화가 많이 진행된 황체세포에서 보다 강한 연색반응을 관찰할 수 있었다. 때로 황체세포에서 유래된 것으로 보이는 간질세포에서도 양성반응을 관찰할 수 있었다. 이외에도 large antral follicle의 여포강에 인접한 과립세포에서 약한 반응을 보여주었으나, 제 1차 여포에서는 양성반응이 나타나지 않았다.

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폐암 환자의 혈청과 조직 표본상에서 Alpha 1-Proteinase Inhibitor의 조사 연구 (Investigation of Alpha 1-Proteinase Inhibitor in Serum and Specimen of Lung Cancer Patients)

  • 김송명
    • Journal of Chest Surgery
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    • 제27권5호
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    • pp.364-373
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    • 1994
  • Alpha 1-Proteinase inhibitor[PI] was known as a major protective enzyme against to excessive hydrolytic and proteolytic reaction. So, it was suggested that Alpha 1-PI may implicated in growth of bronchogenic cancer. This study was undertaken to investigate the role of Alpha 1-PI in local invasion of bronchogenic cancer. Three groups of patients were studied; Preliminary research group of 15 bronchogenic cancer patients, Main research group of 13 bronchogenic cancer patients and Normal control group of 10 nephrectomy donor. Serum Alpha 1-PI level was observed in each group of patients during pre-and postoperative days. Pre-operative serum Alpha 1-PI level in preliminary research group [329.2$\pm$14.21mg/dl]and main research group[406.2$\pm$39.30mg/dl] were higher than in normal control group[236.2$\pm$19.55mg/dl] significantly[p<0.005]. Serial Alpha 1-PI level in each group during pre-and postoperative days shows peaked at 3rd. postoperative day in preliminary and main research group, thereafter decreased gradually. Immunohistochemical study for Alpha 1-antitrypsin[A1AT] was carried out by ABC[avidin-biotin peroxidase complex] method using Alpha-1 antitrypsin DAKOR to tumor tissues of 13 lung cancer patients in main research group. 6 cases[46.2%, squamous cell ca.;5, adenocarcinoma;1] of above 13 cases show positive immunoreactivity for A1AT. In conclusion, alpha 1-PI and elastase are disclosed that have defined actions for lung cancer growing or spreading.

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한국재래산양의 태아 및 신생아 기관의 조직발달에 관한 조직화학적 연구 (Histochemical study on the tracheal development in fetuses and neonates of Korean native goats)

  • 김종섭
    • 대한수의학회지
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    • 제37권2호
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    • pp.235-244
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    • 1997
  • The present study was performed to investigate the patterns of appearance of lectin in trachea of fetuses of 60, 90 and 120 days old and neonates of Korean native goat. Carbohydrate markers were used in histochemistry for the determination of the lectin by staining of avidin-biotin-peroxidase complex(ABC), and the markers consisted of biotin-labeled concanavalin A(Con A), dolichos biflorus agglutinin(DBA), rincinus communis agglutinin(RCA-I), ulexeuropalus communis agglutinin(UEA) and wheat germ agglutinin(WGA). 1. The Con A-binding reactions appeared moderately on the apical surface of the tracheal epithelia in 60 days old fetuses, and the reactions were similar on the tracheal epithelia and glands in 90 and 120 days old fetuses and neonates. 2. Reaction of the DBA appeared as the strongest meanwhile the DBA-binding reactions were determined strongly on the apical surface of the tracheal epithelia in the 60 days old fetuses. Reaction for the DBA on the tracheal epithelia and glands of 90 and 120 days old fetuses and neonates were in same manner. 3. The RCA-I-binding reactions appeared very strongly on the apical surface of the tracheal epithelia in 60 and 90 days old fetuses. Reaction to the RCA-1 appeared moderately on certain apical surface of tracheal epithelia and glands in 120 days old fetuses and neonates. 4. No reactions provoked for the UEA in trachea of 60 days old fetuses and neonates, but the UEA-binding reactions appeared moderately in the tracheal epithelia of 90 days old fetuses and weakly in 120 days old fetuses. 5. The WGA-binding reactions appeared very strongly on the apical surface of the tracheal epithelia in 60 and 90 days old fetuses, and moreover, the reactions were determined on the luminal surface of the tracheal gland in 90 days old fetuses. On the other hand, goblet cells of the tracheal epithelia and glands in neonates reacted moderately to the WGA.

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하악두(下顎頭)의 부분절제(部分切除)된 연골(軟骨) 및 골(骨)의 치유과정(治癒課程)에서 비교원성(非膠原性) 단백질(蛋白質) 분포(分布)에 관(關)한 연구(硏究);주사전자현미경적(走査電子顯微鏡的) 및 면역조직화학적(免疫組織化學的) 연구(硏究) (DISTRIBUTION OF NONCOLLAGENOUS PROTEIN DURING REPAIR OF PARTIALLY RESECTED CONDYLAR CARTILAGE AND BONE;SEM AND IMMUNOHISTOCHEMICAL STUDY)

  • 김명환;이상철
    • Maxillofacial Plastic and Reconstructive Surgery
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    • 제18권3호
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    • pp.411-427
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    • 1996
  • The purpose of this study was to observe the healing process and the distribution of fibronectin in injured condylar cartilage and bone by using LM and SEM. In order to perform this study, 40 male rat, weighing about 250g were selected. Under general anesthesia with Pentobarbital sodium, condylar cartilage and neck bone were resected. Then, the wound was irrigated with saline and closed with 5-0 chromic catgut and 4-0 silk by layer-to-layer suturing. The experimental rats were sacrificed by perfusion with 3% paraformaldehyde at 1st and 4th week after operation. The condylar process and surrounding tissues were cut, demineralized, dehydrated and embedded in paraffin. The histological observation of the specimens in LM level was performed after H-E stain and Azan stain. For localization of fibronectin, immunostaining was achieved by the avidin-biotin complex method. To study the change on condylar surface, the specimens were dehydrated, dried, gold coated and were observed with a scanning electron microscope(Hitachi S-2300). The results were as follows ; 1. The cartilage group and the bone group were repaired with epiphyseal cartilage layer on the cut surface as the normal control group. 2. The cut surface was repaired more quickly in the cartilage group than in the bone group. 3. Chondrocytes, diferentiated during healing, were stained strongly to anti-fibronectin, and fibronectin was supposed to participatein chondrocyte differentiation and cartilagenous matrix formation. 4. Fibronectin was distributed more in the new bone than in the old bone, and the osteoblasts surrounding it were also stained strongly. Fibronectin was supposed to participate in new bone matrix formation. 5. Fibronectin is supposed to be associated with the differentiation, migration and adhesion of chondrocyte and osteoblast and to participate in endochondral bone formation.

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Hep G2 세포와 rat 간세포에서 Metronidazole에 의한 암모니아 독성 감소 (Metronidazole Reduced Ammonia Toxicity in Human Hep G2 cell and Rat Hepatocytes)

  • 김보애;김현정;김유영
    • KSBB Journal
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    • 제23권5호
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    • pp.381-386
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    • 2008
  • 본 연구에서는 암모니아에 의해 손상된 사람의 간세포주 Hep G2 cell과 rat의 hepatocyte에 대하여 metronidazole이 간 세포 손상을 억제하는 효과가 있음을 밝혔다. Metronidazole은 암모니아에 의한 세포 생존율 감소, 배지내의 암모니아 수준 및 지질과산화 증가 및 항산화 효소 발현 감소 그리고 세포 내 DNA 손상과 세포사멸을 억제하였다. 따라서 metronidazole은 암모니아로부터 기인하는 세포손상을 감소시켜 간세포 기능을 보호함으로써 간 기능의 저하로 발생한 과암모니아혈증에 효과적인 치료제로서의 가능성을 시사한다.

기능성 고분자의 세포특이성 재료로의 이용에 관한 연구 (Application of Hepatocyte Specific Polymers with Functional group)

  • 이정복;김재웅
    • 분석과학
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    • 제9권1호
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    • pp.84-90
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    • 1996
  • 본 연구에서는 스티렌 골격에 올리고당 및 비오틴 잔기를 결사슬에 갖는 새로운 세포 특이성 고분자 재료를 설계하여 합성하였다. 이들 고분자 재료를 간세포의 다점 인식 재료로서의 사용 가능성을 검토한 실험 결과를 보고하고자 한다. 간세포의 초기 접착 거동을 조사하기 위하여 합성된 고분자 재료 p(VLA-co- VBA) 90 : 10, p(VLA-co-VBA) 80 : 20 및 대조 물질로 PVLA의 농도가 각각 0.01%(w/v) 되도록 조절하여 1mL 씩 폴리스티렌 페트리 접시에 넣고, 혈청 존재 및 비존재하에서 Seglen법으로 단리한 간세포를 각각 첨가한 결과 60분 경과 후에는 혈청 비존재하에서와 같은 70% 정도의 높은 접착률을 보여 주었다. 폴리머 p(VLA-co-VBA) 70:30에 함유된 비오틴 잔기와 아비딘과의 분자 회합에 의한 응집형상은 UV 투과율의 변화로 확인 하였다.

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체강 삼출액의 세포학적 검사에서의 p53 면역염색의 유용성 (p53 Immunoreactivity in the Cytology of Body Cavity Fluid)

  • 성순희;한운섭
    • 대한세포병리학회지
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    • 제9권1호
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    • pp.15-20
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    • 1998
  • Mutant form of the p53 gene product is abnormally accumulated in the nuclei of the tumor cells due to prolonged half life, and readily detected by immunohistochemical methods. To determine the positivity rate of p53 in body cavity fluid according the primary site and histological types of tumors and the utility of p53 immunostaining as an adjunct in the diagnosis of malignancy, we reviewed 69 effusions, including pleural effusion, ascitic fluid, and pericardial fluid, that were diagnosed as overt malignancy and 21 effusions of suspicious malignancy, immunohistochemistry was performed on paraffin-embedded cell blocks using a monoclonal antibody to p53 supressor gene product(Clone DO7) and a standard avidin-biotin complex technique with a citrate buffer antigen retrieval solution. The results were as follows; of the 46 pleural effusions with overt malignancy, 22 were immunopositive for p53 protein; of the 21 ascitic fluids with overt malignancy, 5 were positive for p53. Positivity rates according to the primary sites of tumors were 18 of 34(52.9%), 8 of 21(38.1%), 1 of 9(11.1%) cases of the tumors of the lung, GI tract, and ovary, respectively. According to the histologic types of lung cancer, 11 cases(61.6%) were positive out of 18 adenocarcinomas, 2 of 5 large cell undifferentiated carcinomas, and 1 of 2 small cell undifferentiated carcinomas. Of 21 cases of suspicious malignancy, 6 were positive for p53 and all of them(6/6) were confirmed as adenocarcinoma of the lung or GI tract. These findings indicate that p53 immunostaining using paraffin embedded cell block is useful diagnostic and prognostic marker in body fluid cytology although negative immunostaining does not exclude malignancy.

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흰쥐 대구치의 치수강 노출 후 치유 및 형성과정에서 치수와 상아질 기질내의 교원질과 당단백의 분포에 관한 면역조직화학적 연구 (FORMATION OF EXTRACELLULAR MATRIX COMPONENTS DURING DEVELOPMENT AND REPAIR OF PERFORATION OF THE RAT DENTIN AND PULP)

  • 김병우;민병순
    • Restorative Dentistry and Endodontics
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    • 제21권1호
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    • pp.35-53
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    • 1996
  • The development and repair requires the formation of new tissues comprised of various extracellular matrix components. The present study investigated the formation and distribution of the major ECM components such as type I collagen, type III collagen, fibronection, bone sialoprotein, and osteonection during development and repair. For developing observation. Sprague-Dawley rats weighing $27{\pm}1gm$ were sacrificed. For repair observation, Sprague-Dawley rats weighing $110{\pm}5gm$ were used. The pulp perforation were prepared on mesial surface of the maxillary first molar by using 1/2round bur. At 5 days after perforation, rats were sacrificed by perfusion with 3 % paroformaldehyde. The maxillary first molar region were cut, demineralized, dehydrated and embedded in paraffin. Immunostaining the ECM components was achieved by the avidin-biotin complex method. The results as follows : 1. Bright immunoreaction for fibronectin was present in the basement membrane at the inner epithelial-mesenchymal interface, especially concentrated in the blood vessel walls, cell membrane of odontoblasts, and initial predentin. 2. Type I and III collagen was observed in the newly formed pulp tissue, predentin, and its intensity increased as more of these components during repair. 3. Strong immunostaining for bone sialoprotein and osteonectin was found in dentin while no or weaker staining was observed loose connective tissue of the pulp. 4. These results suggest that develpment and repair is achieved through a series of cell differentiation and attachment by the specific ECM components.

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구강암 발암과정에서 genistein의 혈관형성 억제에 관한 연구 (ANTI-ANGIOGENIC ACTIVITY OF GENISTEIN IN ORAL CARCINOGENESIS)

  • 송승일;김명진
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
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    • 제30권5호
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    • pp.400-405
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    • 2004
  • Angiogenesis inhibition is major concern to cancer chemotherapy and many studies about compound inhibiting angiogenesis is in progression. The long-known preventive effect of plant-based diet on tumorigenesis and other chronic diseases is well documented. Especially soy extract, genistein, is known to be potent angiogenesis inhibitor and prevent development and progression of tumor. In the present study, the effect of angiogenesis on tumorigenesis and chemopreventive effect of genistein by angiogenesis inhibition in hamster buccal pouch oral carcinigenesis model induced by 7.12-dimethylbenza(a)nthracene (DMBA) was studied. Forty eight Syrian Golden young adult hamsters (150-200 gm) were divided into two groups. In control group, 0.5% DMBA in heavy mineral oil was applied to hamster buccal pouch three times a week and in experimental group, 0.1 mg of genistein is administered orally everyday in addition to DMBA application. The animals were euthanized from 2 weeks to 16 weeks with interval of 2 week. H&E staining and immunohistochemistry was performed to evaluate microvessel density by using factor VIII-related antigen and avidin-biotin technique. Microvessels per area was quantified and compared between control and experimental group statistically. The results were as follows. 1. Microvessel density was increased time dependently in both groups and especially the increase was significant from 12 weeks to 16 weeks. 2. When comparing both group, the experimental group showed significantly low microvessel density than control group in 12 weeks (p=0.043), 14 weeks (p=0.050), 16 weeks (p=0.037). Based on these results, it was concluded that genistein influenced oral carcinogenesis by angiogenesis inhibition.