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N Vanmuylder

Publications and source records attributed to N Vanmuylder.

At least 19 recordsLinked to original sources
PubMed2006

Correlation of Hsp110 expression with caspase-3 and -9 during apoptosis induced by in vivo embryonic exposition to retinoic acid or irradiation in early mouse craniofacial development.

OBJECTIVE: To analyze the expression and role of three proteins (HSP110, caspase-3 and caspase-9) during craniofacial development. DESIGN: Seven pregnant C57Bl/6J mice received, by force-feeding at gestation day 9 (E9), 80 mg/kg of all-trans retinoic acid mixed to sesame oil. Seven pregnant NMRI mice received two grays irradiation at the same gestation day. Control mice of both strains (seven mice for each strain) were not submitted to any treatment. Embryos were obtained at various stages after exposition (3, 6, 12 and 24 h), fixed, dehydrated and embedded. Coronal sections (5 microm) were made. Slide staining occurred alternatively using anti-Hsp110, anti-caspase-3 and anti-caspase-9 immunohistochemistry. RESULTS: Expression of HSP110, caspase-3 and caspase-9 was found in cells of well-known locations of programmed cell death. After retinoic acid exposure, expressions were increased especially in neural crest cells of mandibular and hyoid arches. Quantification of positive cells shows that caspase-9 and Hsp110 were expressed before caspase-3. After irradiation, the expression of the three proteins quickly increased with a maximum 3 h after irradiation. For all three models of apoptosis (physiological, retinoic-induced and irradiation-induced) HSP110 positive cells were more numerous than caspase-3 positive cells. Caspase-3 positive cells were more numerous than caspase-9 positive cells especially in mesectodermal irradiation-induced apoptotic cells. CONCLUSION: The findings show a potential function of HSP110 in apoptosis during embryo development. Caspase-3-expressing cells are more numerous than cells expressing caspase-9, especially irradiation-induced apoptotic neural crest cells. This suggests that other caspases, still to be identified, may activate caspase-3 in this model.

Abnormalities, Drug-Induced↗
PubMed2005

A case with undescended testis, left pelvic kidney and gut malrotation.

We describe here an autopsy case presenting bilateral cryptorchidism, left pelvic kidney and intestinal malrotation, evoking a "reverse rotation" with hypoplasia of the cecum. Furthermore, the colon showed alternate bands of stenosis and dilatation. This association has not yet been described, and is discussed in the light of the embryological events of kidney, gut and gonad development. Two hypotheses can explain gut stenoses (vascular consequences of the malrotation and type Hirschprung aganglionic segments).

Aged↗
PubMed2005

[Expression of caspase 3 and p53 during physiological apoptosis and apoptosis induced by three teratologic agents during early craniofacial development of the mouse embryo].

The neural crest-derived mesectoderm gives rise to physiologic apoptosis areas in early vertebrate embryos. Certain teratologic agents increase this phenomenon. The purpose of this work was to detect caspase 3 (which is associated with the apoptosis cascade) and p53 in cell death areas, both during physiological apoptosis and during apoptosis induced by three agents (retinoic acid, methyl-triazene, irradiation). Antibody revelation was performed using the aBC peroxidase kit. Quantifications were also performed on histological sections. We observed caspase 3 uptake on some apoptotic and preapoptotic cells in control embryos, and in the embryos exposed to the three teratogens. Immunoreactivity generally preceded the development of cytological features of apoptosis. However, p53 was expressed only in the embryos exposed to ionizing radiation and methyl-triazene (an alkylating agent), but not significantly in embryos exposed to retinoic acid. The present results throw some light on apoptosis mechanisms in several teratologic conditions.

Animals↗
PubMed2004

[Histologic and ultrastructural features of cell death both physiological and induced by two different teratogens in branchial arches of mouse embryo].

AIM OF THE STUDY: To observe and compare cell death process both physiological and associated with the administration of two different teratogens (irradiation and retinoic acid) inside cephalic mesectoderm. MATERIAL AND METHODS: Irradiated mice: 2 Gy were administered to E 9 embryos. Retinoic acid: 60 mg/kg were gave to E 8 or E 9 embryos. E 9 - 9.5 and E 10 embryos were removed. E 9 - E 9.5 and E 10 control specimens were collected. We used semi-thin sections and ultra-thin sections observed with transmission electron microscope. RESULTS: The major process is apoptosis, which is increased in experimental embryos compared to control specimens. However, autophagy was observed in retinoic acid-treated embryos, while necrosis can rarely occurs after irradiation. CONCLUSION: If the common process seems to be apoptosis, both teratological models differs owing to their respective secondary features. These differences should be explained by the specific pathogenesis of both teratological agents: ligand-receptor reaction and Hox system disruption in retinoic acid administration, direct aggression against DNA and diffuse cell death process following irradiation. Furthermore, congenital malformations induced by these teratogens are quite different. This can be partially explained by a specific blow of different cellular subpopulations.

Animals↗
PubMed2003

Ectopic stapes: a case report with embryologic correlations.

A case report of unilateral congenital stapes misplacement revealed by computed tomography is presented. In addition to this malformation, the malleus was synostosed to the middle ear roof. This kind of stapes ectopia has not been described previously. We have analyzed the malformative pattern in the light of normal and teratologic development of the stapes. In a teratologic model in which retinoic acid is administered to pregnant mice, we have observed an ectopic stapes primordium independent of the otic capsule. We discuss the possible pathogenesis of this abnormality in terms of the genetic events of middle ear development, which can be perturbed by retinoic acid administration.

Adult↗
PubMed2003

Differential expression of S100 calcium-binding proteins in epidermoid cysts, branchial cysts, craniopharyngiomas and cholesteatomas.

AIMS: To investigate whether epidermoid cysts, branchial cysts, craniopharyngiomas and cholesteatomas express S100 proteins differentially by immunohistochemical assaying the presence of S100A1, S100A2, S100A3, S100A4, S100A5, S100A6 and S100B. METHODS AND RESULTS: Immunopositivity/negativity was recorded for each S100 protein in a series of 52 cases consisting of 12 epidermoid cysts, 12 branchial cysts, 15 adamantinomatous craniopharyngiomas and 13 acquired cholesteatomas. Except in the case of the craniopharyngiomas, immunoreactivity was assessed independently in the basal membrane and the basal, the internal and the keratin layers. Our data show that in contrast to S100B, which was rarely expressed, S100A1, S100A2, S100A4 and S100A5 were often present in these four types of epithelial lesions. S100A3 and S100A6 and, to a lesser extent, S100A5 were the most differentially expressed proteins across the different histopathological groups analysed. These three proteins are expressed more often in craniopharyngiomas and cholesteatomas, the two more aggressive types of lesions. CONCLUSIONS: This is the first study to report data on the expression of seven S100 proteins in different histopathological groups of epithelial head and neck lesions, whose precise embryological origins are still a matter of debate. S100 proteins could possibly be used as markers to target this embryonic origin, since our results show that S100A3 and S100A6 (and, to a lesser extent, S100A5) are expressed differentially across these different groups of epithelial lesions.

Adolescent↗
PubMed2002

Computed tomography of a cyclotocephalic neonate.

Cyclotocephaly is a very rare malformative lethal condition which associates otocephaly (extreme hypoplasia of the mandibular arch with agnathia) and cyclopy with proboscis. The head of a cyclotocephalic neonate from our Museum of Anatomy and Embryology was examined using computed tomography (CT). Cutaneous and osseous three-dimensional reformations were performed. Severe bony malformations were observed. A single orbital cavity was surrounded by a cartilaginous proboscis and a median fusion of maxillae, temporal and zygomatic bones. The single orbital cavity contained both paramedial eyeballs (synophthalmia). The external auditory meati and the ear pinnae were also parasagittal. No oral cavity and mandible were observed. Despite the poor conservation state of the brain, lobar holoprosencephaly was suspected. The mesencephalon and pituitary gland were absent. This exercise could lead to optimizing ultrasonographic prenatal diagnosis.

Abnormalities, Severe Teratoid↗
PubMed2002

[Heat shock proteins, embryogenesis and evolution].

We present results about immunohistochemical identification of several heat shock proteins (HSP'S) during mouse normal and teratological embryogenesis. Apoptotic cells express very specifically and precociously HSP 110. This fact permits to identify apoptotic cells before apparition of morphologic features of apoptosis, but also to quantify the process of cell death in some teratological models, particularly administration of retinoic acid. HSP 86 is expressed in some cell populations, and particularly permanent in germ cells. Our observations brought us to discuss the potential protective role of HSP on germ cells, and the consequence of their inactivation in the macroevolution process, as well as the role of apoptosis in teratology.

Animals↗
PubMed2000

Immunocytochemical investigations of heat shock proteins expression during thymic apoptosis induced by glucocorticoids.

The aim of our study was to investigate a possible expression of different HSPs in rat's thymuses after hydrocortisone administration. The thymuses of 41 young rats (25 to 45 days age old) were studied immunocytochemically: 12 rats were not injected, 8 received an injection of physiological serum, and 21 received HC (125 mg/kg). HSP27, 70 and 110 expression was investigated following the PAP method. HSPs27 were expressed neither in normal thymic lobules nor in the cortical thymic cells after HC injection. HSPs70 were objectivated only in 1 control animal, but were frankly expressed in cortical thymic cells 1 to 48 hours after HC injection and remained significantly expressed until the 7th day after HC injection. HSPs 110 were present in only 1 control animal and appeared to be distinctly expressed 48 hours after HC injection. HSPs 70 and 110 were never expressed in the regenerated thymuses 14 and 21 days after HC injection. This report objectivates for the first time 70 and 110 kDa "stress proteins" expression during the thymic apoptosis induced by glucocorticoids.

Animals↗
PubMed2000

Chaperones in the parotid gland: localization of heat shock proteins in human adult salivary glands.

Heat shock proteins (HSPs) are expressed or increased in response to various biological stresses. Moreover, these 'stress proteins' seem to be expressed by some cells living in physiological conditions. From then on, they could play an important physiological role in normal cell functioning. The best-known physiological role of these HSP proteins is to act as 'molecular chaperones'. In this context, we have investigated the immunohistochemical expression of HSP27, HSP70, HSP90 and HSP110 in 10 human adult salivary glands. To highlight the presence of RNAm encoding HSP70, an in situ hybridization was performed. In our material, HSP27 was strongly expressed in the cytoplasm of striated duct cells and in some myoepithelial cells. The same localization was less stained for HSP70 and HSP90. The immunocytochemical reaction was weak or negative for HSP110 in striated ducts. HSPs were not expressed in acinic cells. In situ hybridization gave a positive signal in striated ducts with a probe encoding HSP70. Epithelial cells of the striated ducts and myoepithelial cells expressed HSP27, HSP70 and HSP90. These HSPs probably act in part as molecular chaperones for protein synthesis, transport and for several interactions between HSPs and different proteins.

Adult↗
PubMed2000

[Expression of heat shock proteins in salivary gland tumors. Immunohistochemical study of HSP27, HSP70, HSP90, and HSP110: apropos of 50 cases].

Heat shock proteins (HSPs) are known to be increased in response to biological stress. Recently some authors described their presence in tumors. Our immunohistochemical investigations revealed the expression of HSP27, HSP70, HSP90 and HSP110 in most of benign tumors of salivary glands (33 cases). In the malignant tumors, the reaction was immunopositive for HSP70 and HSP90 in 13/17 cases; but HSP27 and HSP110 were only expressed in 5/17 cases. In conclusion HSPs were expressed less in malignant than in benign cells. These results suggest that the loss of some HSPs may be a possible sign of malignancy.

HSP110 Heat-Shock Proteins↗
PubMed1998

[The role of apoptosis during craniofacial development: concepts and importance in pathology].

Apoptosis is an essential common final pathway in numerous pathological conditions such as malignant tumors, HIV-related CD4 lymphocytes degeneration, neurodegenerative disorders, and in programmed cell death events during normal embryogenesis. Some teratogenic substances for man and laboratory mammals induce an increase of the apoptotic phenomenon, responsible for the occurrence of some precise cranio-maxillo-facial malformations. The study of cell death during normal or teratogenic embryonic development allows to analyse the cellular mechanisms implied in the control of the apoptotic phenomenon, together with its dysregulation ending in pathological processes. We review the cell death phenomenon during cephalogenesis, both during normal embryogenesis, or in teratogenic conditions known to induce cranio-maxillo-facial malformations.

Abnormalities, Drug-Induced↗
PubMed1998

[Stress proteins: expression of a universal phenomenon of cell defense].

Heat shock proteins or stress proteins play a role in adaptative thermotolerance. All cells, procaryotic and eucaryotic, are able to respond to different cellular aggressions by the synthesis of these stress proteins. In normal physiological conditions, they are considered as "molecular chaperones" Their actual role in pathology is still unknown; some of these heat shock proteins may be correlated with the degree of aggressiveness of some tumors.

Adaptation, Physiological↗
PubMed1997

Strong expression of heat shock proteins in growth plate cartilage, an immunohistochemical study of HSP28, HSP70 and HSP110.

Heat shock proteins (HSPs) are known to be increased in response to stresses. Our immunohistochemical investigations revealed the strong expression of a wide range of HSPs in the chondrocytes of the tibial growth plate cartilage from young rats. HSP28 and HSP70 are expressed in the upper part of the hypertrophic zone of the growth plate cartilage. HSP110 are found from the proliferating zone to the hypertrophic zone. On the other hand, application of the TUNEL method has already shown apoptotic DNA fragmentation in the lower part of the proliferating zone. From then one, HSP expression in the chondrocytes may be correlated with apoptosis, but its possible relation with the different events occurring during the calcification process cannot be excluded.

Animals↗
PubMed1997

Myxomatous odontogenic tumor of the maxilla. An unusual case with squamous and mucoproducing epithelial component.

A tumor attached to the amelo-cemental junction of a third molar impacted in the maxillary tuberosity, consisted histologically of a myxomatous stroma, in which multicystic cavities lined by a columnar epithelium and mucoproducing cells, together with an aggressive squamous epithelial component were present. Although the diagnosis of polyp of the maxillary sinus cannot be excluded, this lesion most likely constitutes an unusual presentation for an odontogenic myxoma of the maxilla, in which an aggressive squamous epithelial component is present, along with a mucosecreting glandular component.

Adult↗