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1.
Eur J Obstet Gynecol Reprod Biol ; 291: 240-246, 2023 Dec.
Article in English | MEDLINE | ID: mdl-37939622

ABSTRACT

OBJECTIVE: Correct referral of women with an ovarian tumor to an oncology department remains challenging. The International Ovarian Tumor Analysis (IOTA) consortium has developed models with higher diagnostic accuracy than the alternative Risk of Malignancy Index (RMI). This study explores the uptake of the IOTA models in Dutch hospitals and factors that impede or promote implementation. Optimal implementation is crucial to improve pre-operative classification of ovarian tumors, which may lead to better patient referral to the appropriate level of care. STUDY DESIGN: In February 2021, an electronic questionnaire consisting of 37 questions was sent to all 72 hospitals in the Netherlands. One pre-selected gynaecologist per hospital was asked to respond on behalf of the department. RESULTS: The study had a response rate of 93% (67/72 hospitals). All respondents (100%) were familiar with the IOTA models with 94% using them in practice. The logistic regression 2 (LR2)-model, Simple ultrasound-based rules (SR) and Assessment of Different NEoplasias in the adneXa (ADNEX) model were used in respectively 40%, 67% and 73% of these hospitals. Respondents rated the models overall with an 8.2 (SD 1.8), 8.3 (SD 1.6) and 8.9 (SD 1.3) respectively for LR2, SR and ADNEX on a scale from 1 to 10. Moreover, 89% indicated to have confidence in the results of the IOTA models. The most important factors to improve further implementation are more training (43%), research on sensitivity, specificity and cost-effectiveness in the Dutch health care system (27%), easier usability (24%) and more consultation time (19%). CONCLUSION: The IOTA ultrasound models are adopted in the majority of Dutch hospitals with the ADNEX model being used the most. While Dutch gynecologists have a strong familiarity and confidence in the models, the uptake varies in reality. Areas that warrant improvement in the Dutch context are more uniformity, education and more research. These findings can be helpful for other countries considering adopting the IOTA models.


Subject(s)
Adnexal Diseases , Ovarian Neoplasms , Female , Humans , Ovarian Neoplasms/diagnostic imaging , Logistic Models , Referral and Consultation , Ultrasonography , Cost-Effectiveness Analysis , Sensitivity and Specificity , Adnexal Diseases/pathology , Diagnosis, Differential
2.
Blood Rev ; 62: 101131, 2023 11.
Article in English | MEDLINE | ID: mdl-37716881

ABSTRACT

BACKGROUND: Optimal peri-operative management for women with Von Willebrand disease (VWD) and heavy menstrual bleeding (HMB) remains undetermined. AIM AND METHODS: To evaluate (pre)operative management in relation to (post)operative bleeding after endometrial ablation (EA) and hysterectomy in VWD women with HMB by performing a database search between 1994 and 2023. RESULTS: Eleven cohort studies and 1 case-report were included, of overall 'low' quality, describing 691 operative procedures. Prophylaxis (Desmopressin, clotting factor concentrates or tranexamic acid) to prevent bleeding was described in 100% (30/30) of EA procedures and in 4% (24/661) of hysterectomies. Bleeding complications despite prophylaxis were described in 13% (3/24) of hysterectomies vs 0% (0/30) in EA. CONCLUSION: VWD women often seem to experience bleeding complications during hysterectomy and all women with VWD received preprocedural hemostatic agents during EA, indicating potential under- and overdosing of current prophylactic strategies. Prospective studies are needed to determine the optimal (pre)operative strategy for gynecological surgical procedures in women with VWD.


Subject(s)
Menorrhagia , Tranexamic Acid , von Willebrand Diseases , Female , Humans , Hemorrhage , Menorrhagia/therapy , Menorrhagia/complications , Prospective Studies , Tranexamic Acid/therapeutic use , von Willebrand Diseases/complications , von Willebrand Diseases/therapy , von Willebrand Factor
3.
Facts Views Vis Obgyn ; 14(4): 299-307, 2022 Dec.
Article in English | MEDLINE | ID: mdl-36724421

ABSTRACT

Background: Endometrial ablation is a frequently performed treatment for heavy menstrual bleeding, but detailed information about recovery to help inform patients is lacking. Objective: To gain more insight into the short-term recovery after NovaSure® endometrial ablation, with the goal of improving preprocedural counselling. Materials and Methods: A total of 61 women who underwent endometrial ablation between March 2019 and November 2021 in a teaching hospital in the Netherlands were included in this prospective cohort study. Main outcome measures: Short-term recovery was investigated through questionnaires in the first week after the procedure. The primary outcome was the Recovery Index (RI-10). Secondary outcomes included health-related quality of life (EQ-5D-5L), pain intensity, use of analgesics, nausea, vaginal discharge, capability of performing activities (domestic chores, sports, work), self-rated health (EQ-VAS) and the feeling of full recovery. Results: A total of 33 women underwent the procedure under local anaesthesia and 28 women under procedural sedation. The RI-10 increased in the first week; median scores on day one, two and seven were 34 (IQR 28.5-41.5), 38.5 (IQR 31-47), and 42 (IQR 37.5-48), respectively. The median time for full recovery was five days. However, 23% of all women were not fully recovered within seven days. Women needed a median time of two days for returning to their work and 5.5 days for sporting activities. There were no differences in recovery between both anaesthesia techniques. Conclusions: Women undergoing endometrial ablation can be informed that most will fully recover within the first week of the procedure and that there is no difference in expected recovery time according to whether the procedure is undertaken with local anaesthesia or conscious sedation. What is New?: The short-term recovery after endometrial ablation has been mapped in this trial. This information can be used in counselling women with heavy menstrual bleeding.

4.
Eur J Obstet Gynecol Reprod Biol ; 254: 206-211, 2020 Nov.
Article in English | MEDLINE | ID: mdl-33011502

ABSTRACT

OBJECTIVE: To evaluate the effect of intrauterine fundal anaesthesia during outpatient endometrial ablation. STUDY DESIGN: A randomised, double-blinded non-inferiority trial was performed in one hospital and one independent treatment center in the Netherlands. A total of 96 women who were planned for a NovaSure® endometrial ablation under local anaesthesia between December 2015 and February 2018 were included in this trial. These women were randomised to paracervical anaesthesia combined with hysteroscopic fundal infiltration with anaesthestics or paracervical anaesthesia combined with hysteroscopic fundal infiltration with saline. The primary outcome was pain during ablation. To study non-inferiority of paracervical anaesthesia without fundal anaesthesia, we assessed the co-primary endpoints Faces Pain Score and Numeric Rating Score. Secondary outcomes included pain scores at other moments during and after the procedure, postoperative use of analgesics, satisfaction, side-effects and complications. The primary outcomes were tested with a non-inferiority margin (2.0 points on changes in pain), and the secondary outcomes were compared using conventional statistical methods. RESULTS: Paracervical anaesthesia without fundal anaesthesia did not establish non-inferiority to the combination of paracervical anaesthesia and fundal infiltration with anaesthetics when both primary outcome variables of pain were taken into account (Numeric Rating Scale 5.0 versus 3.9 (mean difference 1.2 (95% CI 0.1-2.2)) and Faces Pain Score 5.4 versus 4.8 (mean difference 0.6 (95% CI -0.3-1.5))). Secondary pain scores measured during the procedure were higher or similar in women receiving fundal infiltration with saline as compared to women who received fundal infiltration with anaesthetics. After the procedure, there were no differences in reported pain scores, satisfaction, and side-effects. In the group who received fundal infiltration with saline, more women were admitted to the hospital because of severe pain (3 versus 0 women) and endometritis (1 versus 0 women). CONCLUSION: This study did not confirm non-inferiority of paracervical anaesthesia without fundal anaesthesia to the combination of paracervical anaesthesia with fundal anaesthesia in the reduction of pain during endometrial ablation and therefore provides no reason to leave out fundal anaesthesia. We recommend to use fundal anaesthesia combined with paracervical anaesthesia to reduce pain during endometrial ablation in the office.


Subject(s)
Endometrial Ablation Techniques , Analgesics , Anesthesia, Local , Endometrial Ablation Techniques/adverse effects , Female , Humans , Netherlands , Uterus/surgery
5.
Clin Exp Immunol ; 193(3): 361-375, 2018 09.
Article in English | MEDLINE | ID: mdl-29746703

ABSTRACT

Despite advances in our understanding of the mechanisms underlying the progression of chronic kidney disease and the development of fibrosis, only limited efficacious therapies exist. The calcium binding protein S100A8/A9 is a damage-associated molecular pattern which can activate Toll-like receptor (TLR)-4 or receptor for advanced glycation end-products (RAGE). Activation of these receptors is involved in the progression of renal fibrosis; however, the role of S100A8/A9 herein remains unknown. Therefore, we analysed S100A8/A9 expression in patients and mice with obstructive nephropathy and subjected wild-type and S100A9 knock-out mice lacking the heterodimer S100A8/A9 to unilateral ureteral obstruction (UUO). We found profound S100A8/A9 expression in granulocytes that infiltrated human and murine kidney, together with enhanced renal expression over time, following UUO. S100A9 KO mice were protected from UUO-induced renal fibrosis, independently of leucocyte infiltration and inflammation. Loss of S100A8/A9 protected tubular epithelial cells from UUO-induced apoptosis and critical epithelial-mesenchymal transition steps. In-vitro studies revealed S100A8/A9 as a novel mediator of epithelial cell injury through loss of cell polarity, cell cycle arrest and subsequent cell death. In conclusion, we demonstrate that S100A8/A9 mediates renal damage and fibrosis, presumably through loss of tubular epithelial cell contacts and irreversible damage. Suppression of S100A8/A9 could be a therapeutic strategy to halt renal fibrosis in patients with chronic kidney disease.


Subject(s)
Calgranulin A/metabolism , Calgranulin B/metabolism , Epithelial Cells/physiology , Granulocytes/physiology , Kidney/pathology , Ureteral Obstruction/metabolism , Animals , Apoptosis , Calgranulin A/genetics , Calgranulin B/genetics , Cell Polarity , Epithelial-Mesenchymal Transition , Fibrosis , Humans , Mice , Mice, Inbred C57BL , Mice, Knockout
6.
Acta Clin Belg ; 71(2): 107-10, 2016 Apr.
Article in English | MEDLINE | ID: mdl-27075807

ABSTRACT

Distant metastases of meningioma are rare, especially in grade 1 meningiomas. In a recent literature review, only 115 cases were found. In almost all published cases, the meningioma was treated several years before the metastasis was diagnosed. The lungs are the most frequent site of metastasis. We describe two patients treated for meningioma (one case grade 1, the other grade 3) who were referred to the Respiratory Oncology Unit because of the incidental finding of a pulmonary nodule on routine chest radiography. Both had undergone several neurosurgical procedures but the last operation was more than 7 years before in both cases. Positron emission tomography scan was suggestive of a malignant lung tumour. The lesions were surgically removed. Pathology confirmed meningioma in both cases with the same WHO grade, immunohistochemical and genetic profiles as the original meningioma. Both patients recovered well from thoracic surgery. The patient with grade 3 meningioma died three years later from intracranial recurrence. When a patient previously treated for meningioma develops a nodular lung lesion, metastasis of the meningioma should be in the differential diagnosis list. Because of the occurrence of distant metastasis even in grade I meningiomas, we suggest that the grading system should take into account genetic changes in the meningioma. Chromosome 1p and 14q losses possibly explain the aggressive behaviour of the grade 1 meningioma.


Subject(s)
Lung Neoplasms/secondary , Meningeal Neoplasms/pathology , Meningioma/secondary , Solitary Pulmonary Nodule/secondary , Aged , Carcinoembryonic Antigen/blood , Chromosome Deletion , Diagnosis, Differential , Humans , Immunohistochemistry , Lung Neoplasms/diagnosis , Lung Neoplasms/genetics , Lung Neoplasms/pathology , Magnetic Resonance Imaging , Male , Meningeal Neoplasms/diagnosis , Meningeal Neoplasms/surgery , Meningioma/diagnosis , Meningioma/genetics , Meningioma/pathology , Middle Aged , Neoplasm Grading , Neoplasm Recurrence, Local , Optical Imaging , Positron-Emission Tomography , Solitary Pulmonary Nodule/diagnosis , Solitary Pulmonary Nodule/genetics , Solitary Pulmonary Nodule/pathology
7.
J Thromb Haemost ; 14(6): 1171-82, 2016 06.
Article in English | MEDLINE | ID: mdl-26990852

ABSTRACT

UNLABELLED: Essentials Endothelial protein C receptor (EPCR) promotes diabetic nephropathy (DN) outcome improvement. Renal expression and shedding of EPCR were measured in diabetic patients with or without DN. Inhibition of metalloproteinase-driven EPCR shedding restored glomerular endothelium phenotype. EPCR shedding through metalloproteinase ADAM17 contributes to the worsening of DN. SUMMARY: Background Diabetic nephropathy (DN) represents the leading cause of end-stage renal disease. The endothelial protein C receptor (EPCR) and its ligand (activated protein C) have been shown to ameliorate the phenotype of DN in mice. EPCR activity can be regulated by proteolytic cleavage involving ADAMs, yielding a soluble form of EPCR (sEPCR). Objective To characterize the renal expression and shedding of EPCR during DN. Methods EPCR levels were measured in plasma, urine and biopsy samples of diabetic patients with (n = 73) or without (n = 63) DN. ADAM-induced cleavage of EPCR was investigated in vitro with a human glomerular endothelium cell line. Results DN patients showed higher plasma and urinary levels of sEPCR than diabetic controls (112.2 versus 135.2 ng mL(-1) and 94.35 versus 140.6 ng mL(-1) , respectively). Accordingly, glomerular endothelial EPCR expression was markedly reduced in patients with DN, and this was associated with increased glomerular expression of ADAM-17 and ADAM-10. In vitro, EPCR shedding was induced by incubation of glomerular endothelium in high-glucose medium, and this shedding was suppressed by ADAM-17 inhibition or silencing, which led to improved vascular endothelial cadherin (VE-cadherin) expression and reduced mRNA expression of transforming growth factor (TGF)-ß. In addition, EPCR silencing led to minor effects on VE-cadherin but to a significant increase in TGF-ß mRNA expression. Conclusion Inhibition of ADAM-driven glomerular EPCR shedding restored the endothelial phenotype of glomerular endothelium, whereas EPCR silencing led to enhanced expression of TGF-ß, a marker of endothelial-mesenchymal transition. These findings demonstrate that EPCR shedding driven by ADAMs contributes to the worsening of DN.


Subject(s)
Diabetic Nephropathies/metabolism , Endothelial Protein C Receptor/metabolism , Kidney/metabolism , ADAM10 Protein/metabolism , ADAM17 Protein/metabolism , Aged , Amyloid Precursor Protein Secretases/metabolism , Biopsy , Cell Line , Diabetes Mellitus/blood , Diabetes Mellitus/pathology , Diabetes Mellitus/urine , Diabetes Mellitus, Type 2/metabolism , Diabetes Mellitus, Type 2/pathology , Diabetic Nephropathies/pathology , Endothelium/pathology , Female , Gene Silencing , Humans , Kidney Glomerulus/metabolism , Ligands , Male , Membrane Proteins/metabolism , Metalloproteases/metabolism , Middle Aged , Phenotype , RNA, Small Interfering/metabolism , Transforming Growth Factor beta/metabolism
9.
J Small Anim Pract ; 54(5): 258-64, 2013 May.
Article in English | MEDLINE | ID: mdl-23617298

ABSTRACT

OBJECTIVES: To retrospectively assess the relationship between bronchoalveolar lavage fluid analysis and lung function parameters as assessed by means of barometric whole body plethysmography and airway responsiveness testing in cats with chronic bronchial disease and to evaluate the potential application of barometric whole body plethysmography and airway responsiveness testing to distinguish between eosinophilic and non-eosinophilic bronchitis. METHODS: Twelve cats presented for chronic bronchial disease with complete bronchoalveolar lavage fluid and barometric whole body plethysmography data were identified. Cats were retrospectively assigned to eosinophilic bronchitis or non-eosinophilic bronchitis groups on the basis of bronchoalveolar lavage fluid eosinophil percentage (threshold 17%). Airway responsiveness was quantified by calculating the concentration of carbachol-inducing bronchoconstriction (C-Penh-300), defined as a 300% increase of basal enhanced pause (Penh). RESULTS: Log Penh was significantly higher and C-Penh-300 significantly lower in eosinophilic bronchitis cats compared to non-eosinophilic bronchitis cats (P=0·031 and P=0·032, respectively). Bronchoalveolar lavage fluid eosinophil percentage was moderately correlated with log Penh (P=0·012, r=0·70) and showed a weak inverse correlation with C-Penh-300 (P=0·047, r=-0·58). CLINICAL SIGNIFICANCE: This study provides supportive evidence of a correlation between airway eosinophilic inflammation and plethysmographic measures of bronchoconstriction and airway responsiveness. Further investigation of the use of barometric whole body plethysmography to differentiate between forms of chronic bronchial disease in cats is indicated.


Subject(s)
Bronchitis/veterinary , Cat Diseases/diagnosis , Plethysmography, Whole Body/veterinary , Pulmonary Eosinophilia/veterinary , Animals , Bronchitis/diagnosis , Bronchoalveolar Lavage Fluid , Cats , Chronic Disease , Diagnosis, Differential , Female , Male , Plethysmography, Whole Body/methods , Pulmonary Eosinophilia/diagnosis , Respiratory Function Tests/veterinary , Retrospective Studies
10.
Vet J ; 179(3): 443-50, 2009 Mar.
Article in English | MEDLINE | ID: mdl-18037312

ABSTRACT

The aims of this study were firstly to characterise a model of subclinical and reversible bronchial inflammation induced by cadmium chloride inhalation in healthy dogs and then to examine the effect of prednisolone or salbutamol treatment on the resulting bronchitis. The model characterisation and the effects of treatment were studied using clinical symptoms, haematology, thoracic radiography, bronchoscopy and bronchoalveolar lavage, barometric whole-body plethysmography and histamine broncho-provocation tests. In addition, the activity of matrix metalloproteinases (MMP)-2 and -9 were determined in serum and bronchoalveolar lavage fluid (BALF). Cadmium inhalation induced: (1) a transient bronchial inflammation, dominated by neutrophils; (2) a neutrophilia of the blood that persisted for up to 4 weeks; (3) a transient increased bronchial reactivity, and (4) a significant increase in MMP-9 activity in the BALF. Prednisolone treatment reduced the influx of inflammatory cells into the BALF, but not significantly, had no effect on pulmonary function, and did not reduce of airway hypersensitivity. Salbutamol had almost no effect on any of the parameters investigated.


Subject(s)
Albuterol/therapeutic use , Anti-Inflammatory Agents/therapeutic use , Bronchitis/veterinary , Dog Diseases/drug therapy , Prednisolone/therapeutic use , Administration, Inhalation , Animals , Bronchitis/chemically induced , Bronchitis/drug therapy , Bronchitis/enzymology , Bronchoalveolar Lavage Fluid/cytology , Bronchodilator Agents/therapeutic use , Cadmium Chloride , Dog Diseases/chemically induced , Dog Diseases/enzymology , Dogs , Female , Male , Matrix Metalloproteinase 2/metabolism , Matrix Metalloproteinase 9/metabolism , Treatment Outcome
11.
Kidney Int ; 73(12): 1333-5, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18516056

ABSTRACT

Ischemia-reperfusion injury is the leading cause of acute renal failure and determinant of renal-transplant outcome. Although many experimental studies show decreased injury and preserved renal function after dampening of the inflammatory response, surprisingly little progress has been made in the development of novel therapies.


Subject(s)
Graft Rejection/prevention & control , Kidney/blood supply , Nephritis/prevention & control , Renal Insufficiency/prevention & control , Reperfusion Injury/therapy , Animals , Chemokines/metabolism , Cytokines/metabolism , Graft Rejection/etiology , Graft Rejection/metabolism , Humans , Kidney/metabolism , Kidney Transplantation , Mice , Nephritis/etiology , Nephritis/metabolism , Renal Insufficiency/etiology , Renal Insufficiency/metabolism , Reperfusion Injury/complications , Reperfusion Injury/metabolism
13.
Clin Exp Immunol ; 130(1): 32-6, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12296850

ABSTRACT

A T helper (Th) 1 immune response is important for host defense against tuberculosis. The multidrug resistance protein (Mrp) 1 is constitutively present at low levels on Th2 lymphocytes, and is expressed on Th1 lymphocytes upon activation. To determine the role of Mrp1 in the pathogenesis of tuberculosis, Mrp1 deficient (-/-) and normal wild type mice were intranasally infected with Mycobacterium tuberculosis. At 2 weeks after infection, Mrp1(-/-) mice had reduced levels of the Th1 cytokine interferon-gamma and an impaired granuloma formation in their lungs. At 5 weeks postinfection, M. tuberculosis outgrowth was enhanced in lungs and livers of Mrp1(-/-) mice. A more prolonged observation of these mice, up to 4 months, revealed no differences in survival or mycobacterial outgrowth. These data suggest that Mrp1 plays an early but dispensable role in the protective immune response to pulmonary tuberculosis.


Subject(s)
ATP Binding Cassette Transporter, Subfamily B, Member 1/physiology , Tuberculosis, Pulmonary/immunology , ATP Binding Cassette Transporter, Subfamily B, Member 1/deficiency , ATP Binding Cassette Transporter, Subfamily B, Member 1/genetics , Administration, Intranasal , Animals , Interferon-gamma/metabolism , Liver/microbiology , Lung/microbiology , Lung/pathology , Mice , Mice, Knockout , Mycobacterium tuberculosis/growth & development , Mycobacterium tuberculosis/immunology , T-Lymphocyte Subsets/immunology , Th1 Cells/metabolism , Th2 Cells/immunology , Tuberculoma/pathology , Tuberculosis, Pulmonary/pathology
14.
J Immunol ; 166(7): 4604-11, 2001 Apr 01.
Article in English | MEDLINE | ID: mdl-11254718

ABSTRACT

Mycobacterium tuberculosis bacilli are intracellular organisms that reside in phagosomes of alveolar macrophages (AMs). To determine the in vivo role of AM depletion in host defense against M. tuberculosis infection, mice with pulmonary tuberculosis induced by intranasal administration of virulent M. tuberculosis were treated intranasally with either liposome-encapsulated dichloromethylene diphosphonate (AM(-) mice), liposomes, or saline (AM(+) mice). AM(-) mice were completely protected against lethality, which was associated with a reduced outgrowth of mycobacteria in lungs and liver, and a polarized production of type 1 cytokines in lung tissue, and by splenocytes stimulated ex vivo. AM(-) mice displayed deficient granuloma formation, but were more capable of attraction and activation of T cells into the lung and had increased numbers of pulmonary polymorphonuclear cells. These data demonstrate that depletion of AMs is protective during pulmonary tuberculosis.


Subject(s)
Immunosuppression Therapy/methods , Macrophages, Alveolar/immunology , Tuberculosis, Pulmonary/immunology , Tuberculosis, Pulmonary/prevention & control , Administration, Intranasal , Animals , Bronchoalveolar Lavage Fluid/cytology , CD4-CD8 Ratio , Cell Count , Cell Movement/immunology , Cell Separation , Clodronic Acid/administration & dosage , Cytokines/biosynthesis , Female , Liposomes/administration & dosage , Lung/immunology , Lung/metabolism , Lung/pathology , Lymphocyte Activation , Macrophages, Alveolar/drug effects , Macrophages, Alveolar/pathology , Mice , Mice, Inbred BALB C , Mycobacterium tuberculosis , Sodium Chloride/administration & dosage , Spleen/cytology , Spleen/immunology , Spleen/metabolism , T-Lymphocyte Subsets/immunology , Tuberculin/pharmacology , Tuberculosis, Pulmonary/pathology
15.
Am J Pathol ; 153(6): 1813-24, 1998 Dec.
Article in English | MEDLINE | ID: mdl-9846972

ABSTRACT

It is unclear whether the intracardial immune reactivity after heart transplantation influences the peripheral immunological status (activation or nonresponsiveness) of the patient. Co-stimulation and activation-induced cell death (AICD) or apoptosis play an important role in determining the balance between lymphocyte reactivity and nonreactivity. Therefore, we studied the expression of co-stimulatory molecules and the process of apoptosis in biopsies of human heart allografts, using immunohistochemistry. Although a normal expression of co-stimulatory molecules on antigen-presenting cells was observed, the expression of their counter-structures on T cells was absent. This may be due to chronic T cell activation, which can lead to the induction of apoptosis via the Fas/Fas ligand pathway. In the infiltrates, a considerable percentage of the lymphocytes, but not the macrophages, were apoptotic. Apoptosis was confirmed by DNA fragmentation analysis. Increased numbers of Bax-expressing versus decreased numbers of Bcl2-expressing lymphocytes in comparison with normal lymphoid tissue confirmed a imbalance in favor of apoptosis. Apoptosis was biased towards CD4+ T cells (65.7% versus 26.6% in CD8+ T cells). Fas was expressed on most of the infiltrating cells. Fas ligand expression was also observed, not only on most of the T cells but also on all macrophages. Because macrophages were often detected in close contact with T cells, they may play a role in T cell regulation via the Fas/Fas ligand pathway. This study indicates that, during rejection, not only is tissue damage induced by infiltrating T cells, but also the infiltrating lymphocytes themselves are actively down-regulated (eg, AICD) by one another and by macrophages in the infiltrate. This regulatory process may affect the immunological status of the patient after heart transplantation.


Subject(s)
Apoptosis , Graft Rejection/immunology , Heart Transplantation/pathology , Myocardium/pathology , T-Lymphocytes/immunology , Antigens, CD/metabolism , Biopsy , CD4-CD8 Ratio , Fluorescent Antibody Technique, Indirect , Graft Rejection/pathology , Heart Transplantation/immunology , Humans , Immunohistochemistry , In Situ Hybridization , Myocardium/immunology , Proto-Oncogene Proteins/metabolism , Proto-Oncogene Proteins c-bcl-2/metabolism , T-Lymphocytes/pathology , Time Factors , bcl-2-Associated X Protein
16.
Plant Cell ; 4(12): 1495-505, 1992 Dec.
Article in English | MEDLINE | ID: mdl-1334743

ABSTRACT

In this paper, we describe the transformation of regenerable maize tissues by electroporation. In many maize lines, immature zygotic embryos can give rise to embryogenic callus cultures from which plants can be regenerated. Immature zygotic embryos or embryogenic type I calli were wounded either enzymatically or mechanically and subsequently electroporated with a chimeric gene encoding neomycin phosphotransferase (neo). Transformed embryogenic calli were selected from electroporated tissues on kanamycin-containing media and fertile transgenic maize plants were regenerated. The neo gene was transmitted to the progeny of kanamycin-resistant transformants in a Mendelian fashion. This showed that all transformants were nonchimeric, suggesting that transformation and regeneration are a single-cell event. The maize transformation procedure presented here does not require the establishment of genotype-dependent embryogenic type II callus or cell suspension cultures and facilitates the engineering of new traits into agronomically relevant maize inbred lines.


Subject(s)
Plants, Genetically Modified/genetics , Transformation, Genetic , Zea mays/genetics , Base Sequence , Culture Techniques , DNA, Recombinant/genetics , DNA, Single-Stranded , Drug Resistance/genetics , Genetic Markers , Kanamycin/pharmacology , Kanamycin Kinase , Molecular Sequence Data , Phenotype , Phosphotransferases/genetics , Regeneration
18.
Symp Soc Exp Biol ; 45: 271-9, 1991.
Article in English | MEDLINE | ID: mdl-1843413

ABSTRACT

We constructed two chimaeric ribonuclease genes that are specifically expressed in anthers of tobacco and rapeseed plants. The expression of these genes affects the production of functional and viable pollen yielding plants that are male sterile. This dominant gene for nuclear male sterility should facilitate the production of hybrid seed in various crops.


Subject(s)
Nicotiana/genetics , Plants, Toxic , Pollen/genetics , Ribonucleases/genetics , Brassica/genetics , Brassica/physiology , Fertility/genetics , Genetic Engineering , Glucuronidase/genetics , Hybridization, Genetic , Plants, Genetically Modified , Promoter Regions, Genetic , Recombinant Fusion Proteins/genetics , Seeds , Nicotiana/enzymology , Nicotiana/physiology
20.
Plant Physiol ; 87(4): 859-66, 1988 Aug.
Article in English | MEDLINE | ID: mdl-16666238

ABSTRACT

The most abundant isoform of the 2S albumin present in seeds of Arabidopsis thaliana has been sequenced and the corresponding gene isolated. Examination of the protein and DNA sequences allows the determination of the exact proteolytic cleavage sites during posttranslational processing. Like other 2S albumins, that of Arabidopsis is made as a prepropeptide. After removal of the signal peptide, the propeptide is cleaved at four other points, giving two subunits linked by a disulfide bridge(s). Comparison of these cleavage sites with those of 2S albumins of Brassica napus and Bertholletia excelsa suggests that while individual cleavage sites between species are conserved, the four processing sites within a species are not similar, suggesting that up to four different proteases may be involved in processing 2S albumins. The Arabidopsis 2S albumin gene was used to isolate the entire gene family. There are four genes, tightly linked in a tandem array. None of the genes contains an intron. Comparison of the predicted protein sequences shows that only one of the genes can encode the isoform determined by protein analysis to be the most abundant, and therefore this gene is certain to be expressed. It is possible that some or all of the other three genes are also active.

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