19 results on '"Hubeau M"'
Search Results
2. Normalization of11C-autoradiographic images for semi-quantitative analysis of woody tissue photosynthesis
- Author
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Mincke, J., primary, Hubeau, M., additional, Cortyn, J., additional, Brans, B., additional, Vanhove, C., additional, Vandenberghe, S., additional, and Steppe, K., additional
- Published
- 2018
- Full Text
- View/download PDF
3. GIS Education: where are the boundaries?
- Author
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Hubeau, M., de Bakker, M., Toppen, F.J., Reinhardt, W., Steenbergen, T., van Orshoven, J., and Faculteit Ruimtelijke Wetenschappen
- Published
- 2012
4. Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiency
- Author
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Boisson, B, Laplantine, E, Prando, C, Giliani, Silvia Clara, Israelsson, E, Xu, Z, Abhyankar, A, Israel, L, Trevejo Nunez, G, Bogunovic, D, Cepika, Am, Macduff, D, Chrabieh, M, Hubeau, M, Bajolle, F, Debre, M, Mazzolari, Evelina, Vairo, Donatella, Agou, F, Virgin, Hw, Bossuyt, X, Rambaud, C, Facchetti, Fabio, Bonnet, D, Quartier, P, Fournet, Jc, Pascual, V, Chaussabel, D, Notarangelo, Luigi Daniele, Puel, A, Israeimmunodeficiency, Autoinflammation, amylopectinosis in humans with inherited HOIL, 1, LUBAC deficiencyl, A, Casanova, Jl, and Picard, C.
- Published
- 2012
5. IRF8 mutations and human dendritic-cell immunodeficiency
- Author
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Hambleton S, Salem S, Bustamante J, Bigley V, Boisson-Dupuis S, Azevedo J, Fortin A, Haniffa M, Ceron-Gutierrez L, Bacon CM, Menon G, Trouillet C, McDonald D, Carey P, Ginhoux F, Alsina L, Zumwalt TJ, Kong XF, Kumararatne D, Butler K, Hubeau M, Feinberg J, Al-Muhsen S, Cant A, Abel L, Chaussabel D, Doffinger R, Talesnik E, Grumach A, Duarte A, Abarca K, Moraes-Vasconcelos D, Burk D, Berghuis A, Geissmann F, Collin M, Casanova JL, and Gros P
- Published
- 2011
6. Plant-water relations of the mangrove species Rhizophora stylosa: a unique story
- Author
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Hubeau, M., Vandegehuchte, M. W., Guyot, A., Catherine Lovelock, Lockington, D. A., and Steppe, K.
7. Plant-PET to investigate phloem vulnerability to drought in Populus tremula under changing climate regimes.
- Author
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Hubeau M, Mincke J, Vanhove C, Courtyn J, Vandenberghe S, and Steppe K
- Subjects
- Carbon metabolism, Carbon Dioxide metabolism, Plant Leaves metabolism, Positron-Emission Tomography, Climate Change, Droughts, Phloem metabolism, Populus metabolism, Trees metabolism
- Abstract
Phloem transport is of great importance in trees to distribute assimilated carbon across the entire tree. Nevertheless, knowledge of phloem is incomplete, because of the complexity of measuring its transport and characteristics. Only few studies have addressed how phloem transport might alter under climatic changes, with most data originating from theoretical studies. We measured phloem characteristics in leaves of young Populus tremula L. trees grown during 5 months under ambient (TA, 404 ppm ± 5) and elevated (TE, 659 ppm ± 3) atmospheric CO2 concentration ([CO2]) using a combination of positron emission tomography (PET) and compartmental modelling. Short-term phloem dynamics were measured in vivo and non-invasively using the short-lived isotope of carbon, 11C (half-life 20.4 min). Trees were scanned in well-watered and dry conditions to assess changes in phloem characteristics induced by drought. Reliability of the PET-derived results was verified with reported observations in the literature. Phloem speed was highest in well-watered TE trees and strongly reduced by 81% under drought, whereas phloem speed reduced by 61% in TA trees at the same level of drought. These findings led us to speculate that phloem transport in TE trees might be more vulnerable to drought. We discuss how a higher phloem vulnerability to drought in a changing climate could impact tree hydraulic functioning. Taken together our results suggest that trees grown for 5 months under elevated [CO2] seem to be less well-acclimated to face projected hotter droughts in a changing climate., (© The Author(s) 2018. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.)
- Published
- 2019
- Full Text
- View/download PDF
8. Cambial pinning relates wood anatomy to ecophysiology in the African tropical tree Maesopsis eminii.
- Author
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Van Camp J, Hubeau M, Van den Bulcke J, Van Acker J, and Steppe K
- Subjects
- Plant Stems anatomy & histology, Plant Stems growth & development, Plant Stems physiology, Rhamnaceae growth & development, Uganda, Wood analysis, Wood physiology, Droughts, Rhamnaceae anatomy & histology, Rhamnaceae physiology, Water metabolism, Wood growth & development
- Abstract
A better understanding and prediction of the impact of changing climate on tree stem growth could greatly benefit from the combination of anatomical and ecophysiological knowledge, yet the majority of studies focus on one research field only. We propose an approach that combines the method of pinning (cambial wounding) to timestamp anatomical X-ray computed microtomography images with continuous measurements of sap flow and stem diameter variations. By pinning the cambium of well-watered and drought-treated young African tropical trees of the species Maesopsis eminii Engl. we could quantify wood formation during a specific period of time and relate it to tree physiology and prevailing microclimate. Integrating continuous plant measurements and high-frequency pinning proved very useful to visualize and quantify the effects on stem growth of drought in M. eminii. Wood formation completely stopped during drought, and was associated with a strong shrinkage in stem diameter. Next, an unexpected increase in stem diameter was observed during drought, probably caused by root pressure, but not accompanied by wood formation. Our proposed approach of combining continuous plant measurements with cambial pinning is very promising to relate ecophysiology to stem anatomy and to understand the mechanisms underlying tree stem growth and bridge the gaps between the two research fields., (© The Author 2017. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.)
- Published
- 2018
- Full Text
- View/download PDF
9. Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases.
- Author
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Conti F, Lugo-Reyes SO, Blancas Galicia L, He J, Aksu G, Borges de Oliveira E Jr, Deswarte C, Hubeau M, Karaca N, de Suremain M, Guérin A, Baba LA, Prando C, Guerrero GG, Emiroglu M, Öz FN, Yamazaki Nakashimada MA, Gonzalez Serrano E, Espinosa S, Barlan I, Pérez N, Regairaz L, Guidos Morales HE, Bezrodnik L, Di Giovanni D, Dbaibo G, Ailal F, Galicchio M, Oleastro M, Chemli J, Danielian S, Perez L, Ortega MC, Soto Lavin S, Hertecant J, Anal O, Kechout N, Al-Idrissi E, ElGhazali G, Bondarenko A, Chernyshova L, Ciznar P, Herbigneaux RM, Diabate A, Ndaga S, Konte B, Czarna A, Migaud M, Pedraza-Sánchez S, Zaidi MB, Vogt G, Blanche S, Benmustapha I, Mansouri D, Abel L, Boisson-Dupuis S, Mahlaoui N, Bousfiha AA, Picard C, Barbouche R, Al-Muhsen S, Espinosa-Rosales FJ, Kütükçüler N, Condino-Neto A, Casanova JL, and Bustamante J
- Subjects
- BCG Vaccine administration & dosage, Bacterial Infections diagnosis, Bacterial Infections epidemiology, Bacterial Infections etiology, Bacterial Infections mortality, Child, Child, Preschool, Female, Granulomatous Disease, Chronic epidemiology, Granulomatous Disease, Chronic mortality, Granulomatous Disease, Chronic therapy, Humans, Infant, Male, Mycobacterium Infections epidemiology, Mycobacterium Infections mortality, Mycoses diagnosis, Mycoses epidemiology, Mycoses etiology, Mycoses mortality, Patient Outcome Assessment, Retrospective Studies, Tuberculosis diagnosis, Tuberculosis etiology, Granulomatous Disease, Chronic complications, Mycobacterium Infections diagnosis, Mycobacterium Infections etiology
- Abstract
Background: Chronic granulomatous disease (CGD) is a rare primary immunodeficiency caused by inborn errors of the phagocyte nicotinamide adenine dinucleotide phosphate oxidase complex. From the first year of life onward, most affected patients display multiple, severe, and recurrent infections caused by bacteria and fungi. Mycobacterial infections have also been reported in some patients., Objective: Our objective was to assess the effect of mycobacterial disease in patients with CGD., Methods: We analyzed retrospectively the clinical features of mycobacterial disease in 71 patients with CGD. Tuberculosis and BCG disease were diagnosed on the basis of microbiological, pathological, and/or clinical criteria., Results: Thirty-one (44%) patients had tuberculosis, and 53 (75%) presented with adverse effects of BCG vaccination; 13 (18%) had both tuberculosis and BCG infections. None of these patients displayed clinical disease caused by environmental mycobacteria, Mycobacterium leprae, or Mycobacterium ulcerans. Most patients (76%) also had other pyogenic and fungal infections, but 24% presented solely with mycobacterial disease. Most patients presented a single localized episode of mycobacterial disease (37%), but recurrence (18%), disseminated disease (27%), and even death (18%) were also observed. One common feature in these patients was an early age at presentation for BCG disease. Mycobacterial disease was the first clinical manifestation of CGD in 60% of these patients., Conclusion: Mycobacterial disease is relatively common in patients with CGD living in countries in which tuberculosis is endemic, BCG vaccine is mandatory, or both. Adverse reactions to BCG and severe forms of tuberculosis should lead to a suspicion of CGD. BCG vaccine is contraindicated in patients with CGD., (Copyright © 2016 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.)
- Published
- 2016
- Full Text
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10. Plant-PET Scans: In Vivo Mapping of Xylem and Phloem Functioning.
- Author
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Hubeau M and Steppe K
- Subjects
- Biological Transport, Plant Leaves metabolism, Plant Stems metabolism, Water metabolism, Phloem metabolism, Plants metabolism, Positron-Emission Tomography methods, Xylem metabolism
- Abstract
Medical imaging techniques are rapidly expanding in the field of plant sciences. Positron emission tomography (PET) is advancing as a powerful functional imaging technique to decipher in vivo the function of xylem water flow (with (15)O or (18)F), phloem sugar flow (with (11)C or (18)F), and the importance of their strong coupling. However, much remains to be learned about how water flow and sugar distribution are coordinated in intact plants, both under present and future climate regimes. We propose to use PET analysis of plants (plant-PET) to visualize and generate these missing data about integrated xylem and phloem transport. These insights are crucial to understanding how a given environment will affect plant physiological processes and growth., (Copyright © 2015 Elsevier Ltd. All rights reserved.)
- Published
- 2015
- Full Text
- View/download PDF
11. Phagocyte nicotinamide adenine dinucleotide phosphate oxidase activity in patients with inherited IFN-γR1 or IFN-γR2 deficiency.
- Author
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Conti F, Aragão Filho WC, Prando C, Deswarte C, Hubeau M, Newburger PE, Casanova JL, Bustamante J, and Condino-Neto A
- Subjects
- Humans, Mycobacterium Infections immunology, Phagocytes immunology, Interferon gamma Receptor, Genetic Predisposition to Disease, Mycobacterium Infections enzymology, Mycobacterium Infections genetics, NADPH Oxidases metabolism, Phagocytes enzymology, Receptors, Interferon deficiency
- Published
- 2015
- Full Text
- View/download PDF
12. Modelling reveals endogenous osmotic adaptation of storage tissue water potential as an important driver determining different stem diameter variation patterns in the mangrove species Avicennia marina and Rhizophora stylosa.
- Author
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Vandegehuchte MW, Guyot A, Hubeau M, De Swaef T, Lockington DA, and Steppe K
- Subjects
- Avicennia anatomy & histology, Avicennia growth & development, Environment, Osmosis, Plant Stems anatomy & histology, Plant Stems growth & development, Plant Stems physiology, Rhizophoraceae anatomy & histology, Rhizophoraceae growth & development, Xylem anatomy & histology, Xylem growth & development, Xylem physiology, Adaptation, Physiological, Avicennia physiology, Models, Biological, Rhizophoraceae physiology, Water physiology
- Abstract
Background: Stem diameter variations are mainly determined by the radial water transport between xylem and storage tissues. This radial transport results from the water potential difference between these tissues, which is influenced by both hydraulic and carbon related processes. Measurements have shown that when subjected to the same environmental conditions, the co-occurring mangrove species Avicennia marina and Rhizophora stylosa unexpectedly show a totally different pattern in daily stem diameter variation., Methods: Using in situ measurements of stem diameter variation, stem water potential and sap flow, a mechanistic flow and storage model based on the cohesion-tension theory was applied to assess the differences in osmotic storage water potential between Avicennia marina and Rhizophora stylosa., Key Results: Both species, subjected to the same environmental conditions, showed a resembling daily pattern in simulated osmotic storage water potential. However, the osmotic storage water potential of R. stylosa started to decrease slightly after that of A. marina in the morning and increased again slightly later in the evening. This small shift in osmotic storage water potential likely underlaid the marked differences in daily stem diameter variation pattern between the two species., Conclusions: The results show that in addition to environmental dynamics, endogenous changes in the osmotic storage water potential must be taken into account in order to accurately predict stem diameter variations, and hence growth.
- Published
- 2014
- Full Text
- View/download PDF
13. Influence of human activity patterns on epidemiology of plague in Western Usambara Mountains, Tanzania.
- Author
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Hubeau M, Gulinck H, Kimaro DN, Hieronimo P, and Meliyo J
- Subjects
- Geography, Humans, Remote Sensing Technology, Tanzania epidemiology, Human Activities, Plague epidemiology
- Abstract
Human plague has been a recurring public health threat in some villages in the Western Usambara Mountains, Tanzania, in the period between 1980 and 2004. Despite intensive past biological and medical research, the reasons for the plague outbreaks in the same set of villages remain unknown. Plague research needs to broaden its scope and formulate new hypotheses. This study was carried out to establish relationships between the nature and the spatial extent of selected human activities on one hand, and the reported plague cases on the other hand. Three outdoor activities namely, fetching water, collecting firewood and going to the market, were selected. Through enquiries the activity patterns related to these activities were mapped in 14 villages. Standard deviation ellipses represent the extent of action spaces. Over 130 activity types were identified and listed. Of these, fetching water, collecting firewood and going to the market were used for further analysis. The results indicate a significant correlation between the plague frequency and the size of these action spaces. Different characteristics of land use and related human activities were correlated with the plague frequency at village and hamlet levels. Significant relationships were found between plague frequency and specific sources of firewood and water, and specific market places.
- Published
- 2014
- Full Text
- View/download PDF
14. Chronic granulomatous disease in Morocco: genetic, immunological, and clinical features of 12 patients from 10 kindreds.
- Author
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Baba LA, Ailal F, El Hafidi N, Hubeau M, Jabot-Hanin F, Benajiba N, Aadam Z, Conti F, Deswarte C, Jeddane L, Aglaguel A, El Maataoui O, Tissent A, Mahraoui C, Najib J, Martinez-Barricarte R, Abel L, Habti N, Saile R, Casanova JL, Bustamante J, Salih Alj H, and Bousfiha AA
- Subjects
- Adolescent, Alleles, Aspergillosis complications, Aspergillosis immunology, Aspergillosis pathology, Bacterial Infections complications, Bacterial Infections immunology, Bacterial Infections pathology, Child, Child, Preschool, DNA Mutational Analysis, Female, Genes, Recessive, Granulomatous Disease, Chronic complications, Granulomatous Disease, Chronic immunology, Granulomatous Disease, Chronic pathology, Humans, Infant, Infant, Newborn, Male, Mutation, NADPH Oxidase 2, Pedigree, Aspergillosis genetics, Bacterial Infections genetics, Granulomatous Disease, Chronic genetics, Membrane Glycoproteins genetics, NADPH Oxidases genetics
- Abstract
Purpose: Chronic granulomatous disease (CGD) is characterized by an inability of phagocytes to produce reactive oxygen species (ROS), which are required to kill some microorganisms. CGD patients are known to suffer from recurrent bacterial and/or fungal infections from the first year of life onwards. From 2009 to 2013, 12 cases of CGD were diagnosed in Morocco. We describe here these Moroccan cases of CGD., Methods: We investigated the genetic, immunological and clinical features of 12 Moroccan patients with CGD from 10 unrelated kindreds., Results: All patients were children suffering from recurrent bacterial and/or fungal infections. All cases displayed impaired NADPH oxidase activity in nitroblue tetrazolium (NBT), dihydrorhodamine (DHR) or 2',7' dichlorofluorescein diacetate (DCFH-DA) assays. Mutation analysis revealed the presence of four different mutations of CYBB in four kindreds, a recurrent mutation of NCF1 in three kindreds, and a new mutation of NCF2 in three patients from a single kindred. A large deletion of CYBB gene has detected in a patient. The causal mutation in the remaining one kindred was not identified., Conclusion: The clinical features and infectious agents found in these patients were similar to those in CGD patients from elsewhere. The results of mutation analysis differed between kindreds, revealing a high level of genetic and allelic heterogeneity among Moroccan CGD patients. The small number of patients in our cohort probably reflects a lack of awareness of physicians. Further studies on a large cohort are required to determine the incidence and prevalence of the disease, and to improve the description of the genetic and clinical features of CGD patients in Morocco.
- Published
- 2014
- Full Text
- View/download PDF
15. Plant-water relations of the mangrove species Rhizophora stylosa: a unique story.
- Author
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Hubeau M, Vandegehuchte MW, Guyot A, Lovelock CE, Lockington DA, and Steppe K
- Subjects
- Ecosystem, Rhizophoraceae growth & development, Trees growth & development, Rhizophoraceae metabolism, Trees metabolism, Water metabolism
- Published
- 2014
16. Variant of X-Linked Chronic Granulomatous Disease Revealed by a Severe Burkholderia cepacia Invasive Infection in an Infant.
- Author
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Lugo Reyes SO, Mahlaoui N, Prando C, Blancas Galicia L, Hubeau M, Blanche S, Picard C, Casanova JL, and Bustamante J
- Abstract
Chronic granulomatous disease (CGD) is a primary immunodeficiency characterized by increased susceptibility to bacteria and fungi since early in life, caused by mutations in any of the five genes coding for protein subunits in NADPH oxidase. X-linked variant CGD can be missed during routine evaluation or present later in life due to hypomorphic mutations and a residual superoxide production. The case of a 10-month-old boy who died of pneumonia is reported. The isolation of Burkholderia cepacia from his lung, together with a marginally low nitroblue tetrazolium reduction assay (NBT), made us suspect and pursue the molecular diagnosis of CGD. A postmortem genetic analysis finally demonstrated CGD caused by a hypomorphic missense mutation with normal gp91 (phox) expression. In a patient being investigated for unusually severe or recurrent infection, a high index of suspicion of immunodeficiency must be maintained.
- Published
- 2013
- Full Text
- View/download PDF
17. Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiency.
- Author
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Boisson B, Laplantine E, Prando C, Giliani S, Israelsson E, Xu Z, Abhyankar A, Israël L, Trevejo-Nunez G, Bogunovic D, Cepika AM, MacDuff D, Chrabieh M, Hubeau M, Bajolle F, Debré M, Mazzolari E, Vairo D, Agou F, Virgin HW, Bossuyt X, Rambaud C, Facchetti F, Bonnet D, Quartier P, Fournet JC, Pascual V, Chaussabel D, Notarangelo LD, Puel A, Israël A, Casanova JL, and Picard C
- Subjects
- Bacterial Infections genetics, Bacterial Infections immunology, Cell Cycle Proteins genetics, Cell Line, Fibroblasts immunology, Fibroblasts metabolism, Humans, Immunologic Deficiency Syndromes metabolism, Interleukin-1beta metabolism, Monocytes immunology, Monocytes metabolism, Oligonucleotide Array Sequence Analysis, Protein Serine-Threonine Kinases antagonists & inhibitors, Protein Serine-Threonine Kinases genetics, Repressor Proteins genetics, Transcription Factors, Ubiquitin-Protein Ligases deficiency, Ubiquitin-Protein Ligases metabolism, Ubiquitination, Glycogen Storage Disease Type IV genetics, Hereditary Autoinflammatory Diseases genetics, Immunologic Deficiency Syndromes genetics, NF-kappa B metabolism, Ubiquitin-Protein Ligases genetics
- Abstract
We report the clinical description and molecular dissection of a new fatal human inherited disorder characterized by chronic autoinflammation, invasive bacterial infections and muscular amylopectinosis. Patients from two kindreds carried biallelic loss-of-expression and loss-of-function mutations in HOIL1 (RBCK1), a component of the linear ubiquitination chain assembly complex (LUBAC). These mutations resulted in impairment of LUBAC stability. NF-κB activation in response to interleukin 1β (IL-1β) was compromised in the patients' fibroblasts. By contrast, the patients' mononuclear leukocytes, particularly monocytes, were hyper-responsive to IL-1β. The consequences of human HOIL-1 and LUBAC deficiencies for IL-1β responses thus differed between cell types, consistent with the unique association of autoinflammation and immunodeficiency in these patients. These data suggest that LUBAC regulates NF-κB-dependent IL-1β responses differently in different cell types.
- Published
- 2012
- Full Text
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18. New mechanism of X-linked anhidrotic ectodermal dysplasia with immunodeficiency: impairment of ubiquitin binding despite normal folding of NEMO protein.
- Author
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Hubeau M, Ngadjeua F, Puel A, Israel L, Feinberg J, Chrabieh M, Belani K, Bodemer C, Fabre I, Plebani A, Boisson-Dupuis S, Picard C, Fischer A, Israel A, Abel L, Veron M, Casanova JL, Agou F, and Bustamante J
- Subjects
- Blotting, Western, Ectodermal Dysplasia 1, Anhidrotic metabolism, Enzyme Activation genetics, Female, Humans, I-kappa B Kinase metabolism, Immunologic Deficiency Syndromes metabolism, Male, Mutation, Missense, NF-kappa B metabolism, Pedigree, Protein Binding, Protein Folding, Signal Transduction genetics, Young Adult, Ectodermal Dysplasia 1, Anhidrotic genetics, I-kappa B Kinase genetics, Immunologic Deficiency Syndromes genetics, Ubiquitin metabolism
- Abstract
Nuclear factor-κB essential modulator (NEMO), the regulatory subunit of the IκB kinase complex, is a critical component of the NF-κB pathway. Hypomorphic mutations in the X-linked human NEMO gene cause various forms of anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID). All known X-linked EDA-ID-causing mutations impair NEMO protein expression, folding, or both. We describe here 2 EDA-ID-causing missense mutations that affect the same residue in the CC2-LZ domain (D311N and D311G) that do not impair NEMO production or folding. Structural studies based on pull-down experiments showed a defect in noncovalent interaction with K63-linked and linear polyubiquitin chains for these mutant proteins. Functional studies on the patients' cells showed an impairment of the classic NF-κB signaling pathways after activation of 2 NEMO ubiquitin-binding-dependent receptors, the TNF and IL-1β receptors, and in the CD40-dependent NF-κB pathway. We report the first human NEMO mutations responsible for X-linked EDA-ID found to affect the polyubiquitin binding of NEMO rather than its expression and folding. These experiments demonstrate that the binding of human NEMO to polyubiquitin is essential for NF-κB activation. They also demonstrate that the normal expression and folding of NEMO do not exclude a pathogenic role for NEMO mutations in patients with EDA-ID.
- Published
- 2011
- Full Text
- View/download PDF
19. Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease.
- Author
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Bustamante J, Arias AA, Vogt G, Picard C, Galicia LB, Prando C, Grant AV, Marchal CC, Hubeau M, Chapgier A, de Beaucoudrey L, Puel A, Feinberg J, Valinetz E, Jannière L, Besse C, Boland A, Brisseau JM, Blanche S, Lortholary O, Fieschi C, Emile JF, Boisson-Dupuis S, Al-Muhsen S, Woda B, Newburger PE, Condino-Neto A, Dinauer MC, Abel L, and Casanova JL
- Subjects
- Animals, CHO Cells, Cricetinae, Cricetulus, Humans, Male, Mutation, NADPH Oxidase 2, NADPH Oxidases immunology, Genes, X-Linked, Genetic Predisposition to Disease, Macrophages immunology, Membrane Glycoproteins genetics, NADPH Oxidases genetics, Tuberculosis genetics
- Abstract
Germline mutations in CYBB, the human gene encoding the gp91(phox) subunit of the phagocyte NADPH oxidase, impair the respiratory burst of all types of phagocytes and result in X-linked chronic granulomatous disease (CGD). We report here two kindreds in which otherwise healthy male adults developed X-linked recessive Mendelian susceptibility to mycobacterial disease (MSMD) syndromes. These patients had previously unknown mutations in CYBB that resulted in an impaired respiratory burst in monocyte-derived macrophages but not in monocytes or granulocytes. The macrophage-specific functional consequences of the germline mutation resulted from cell-specific impairment in the assembly of the NADPH oxidase. This 'experiment of nature' indicates that CYBB is associated with MSMD and demonstrates that the respiratory burst in human macrophages is a crucial mechanism for protective immunity to tuberculous mycobacteria.
- Published
- 2011
- Full Text
- View/download PDF
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