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J Bride

Publications and source records attributed to J Bride.

At least 19 recordsLinked to original sources
PubMed2004

Comparing the contractile properties of human fibroblasts in leg ulcers with normal fibroblasts.

OBJECTIVE: The tissue contraction phenomenon associated with wound healing is of prime importance for wound closure. Contractile properties of human fibroblasts from chronic venous leg ulcers were compared with those of normal fibroblasts using in vitro models. METHOD: Biopsies were taken from the uninvolved skin of the thigh, the epithelialised ulcer edge and the non-epithelialised ulcer centre in four patients (average age: 78 years). Fibroblasts were obtained by an explant technique and expanded in vitro in Dulbecco's Modified Eagle's Medium supplemented with 10% foetal calf serum and used for the assays at their fourth passage. Intracellular alpha-smooth muscle actin expression (alphaSM-actin) was studied by immunofluorescence labelling of cells cultured in monolayer. Contractile properties were evaluated using three-dimensional collagen lattices. RESULTS: Fibroblasts from the ulcer centre were the richest cells in actin filaments. Both populations of venous ulcer fibroblasts contracted more rapidly and to a greater extent than normal fibroblasts. The peak contractile forces developed by fibroblasts from the ulcer centre and the ulcer edge were 30% and 18% greater than normal fibroblasts respectively. CONCLUSION: Some functions of fibroblasts, in particular the generation of contractile forces and the formation of cytoplasmic actin filaments, seem not to be affected in chronic venous ulcers. DECLARATION OF INTEREST: This study was supported by the Fondation Coloplast pour la Qualite de la Vie of France.

Actin Cytoskeleton↗
PubMed2003

Comparison of different wound dressings on cultured human fibroblasts and collagen lattices.

OBJECTIVE: We compared the effects on cultured human fibroblasts of a new non-adhesive wound dressing, Urgotul, with five other wound dressings. Urgotul is a hydrocolloid dressing; the comparator dressings included impregnated gauze and modern wound dressings. METHOD: Cultures in monolayer were used to study the morphology and growth of fibroblasts. The Bell model of cultured dermis equivalents was used to investigate myofibroblast differentiation. These cultures were labelled a-SM actin and F-actin. RESULTS: Two of the tested dressings induced cytotoxic effects. They were found to inhibit cell growth (greater than 60%) and to disturb cell shape and cytoskeletal differentiation. Urgotul and the remaining three dressings showed no effect on proliferation. However, some of them modified fibroblast morphology and affected F-actin distribution. CONCLUSION: Depending on their nature and components, wound dressings may respect or affect fibroblast behaviour in vitro (proliferation, morphology and a-SM actin and F-actin distribution). The significance of these in vitro observed findings require further investigations.

Actins↗
PubMed2002

Assessment of collagen lattice thickness by B-scan echography.

BACKGROUND/AIMS: Collagen lattices are an in vitro dermal equivalent that has led to the development of an original model of dermal tissue. Fibroblasts cultured in three-dimensions in a collagen matrix differentiate similarly to in vivo. New technological performances in ultrasonic imaging can now provide precise measurements of tissue thickness with good resolution. The aim of this study was to assess, by B-scan echography, the correlation between collagen lattice thickness and various collagen and cell concentrations. METHODS: Three concentrations of human dermal fibroblasts (F1 = 8.10(5)C/mL, F2 = 16.10(5)C/mL, F3 = 32.10(5)C/mL) and three concentrations of rat tail collagen (C1 = 2 mg mL(-1), C2 = 3 mg mL(-1), C3 = 4 mg mL(-1)) were prepared for five different kinds of collagen lattices: F(2)C(1), F(2)C(2), F(2)C(3), F(1)C(1) and F(3)C(1) (n = 5 per case). Ultrasonic imaging was performed on day 0, 4, 6, 10, 12 and 14 using a Dermcup 2020 scanner. The scans measured thickness in the centre and periphery of the lattice. RESULTS: The collagen lattice echogenicity was similar to a dermis in vivo. For each assessment, the collagen lattice thickness increased until day 12 and then stabilized. The lattice was thicker when the cellular concentration was higher, (at day 14: F(1C1) = 0.66 mm, F(2C1) = 0.86 mm, F(3C1) = 1.21 mm). The collagen concentration did not significantly influence lattice thickness. CONCLUSION: Collagen lattice thickness increased with retraction time and cellular concentration.

Animals↗
PubMed2001

The sibling species Drosophila melanogaster and Drosophila simulans differ in the expression profile of glutathione S-transferases.

Two major forms of glutathione S-transferase are known in Drosophila melanogaster: GST D and GST 2. In the present paper we report the existence of a third major form of glutathione S-transferase in Drosophila simulans. Induction with phenobarbital revealed a different regulation of GST between these species. Despite the fact that these two species are closely related, there was a difference in the expression profile of the enzyme implicated in the detoxification system, suggesting variations in capacity to suit their environment.

Animals↗
PubMed2001

[Mechanical behavior of fibroblasts included in collagen lattices].

Striae distensae are characterized by linear, smooth bands of atrophic-appearing skin. Excessive steroid activity, genetic and mechanical factors and inherited defects of connective tissues are the most frequent causes of this disease. Fibroblasts derived from women presenting striae distensae lesions were included into collagen gels to study their mechanical behavior: capacity to contract free-floating lattices and to produce isometric force in tense lattices. To measure the retracted lattice diameter, the culture dishes were placed on a transparent metric scale. An isometric force system was used to study quantitatively the forces developed during lattice contraction. alpha 2 beta 1 integrins expression (transmembrane receptors) was evaluated by flux cytometry. Striae distensae fibroblasts contract collagen gels slower than normal human fibroblasts but the final contraction is similar. They produce a greater isometric force which is associated with enhanced alpha 2 beta 1 integrins expression. By their mechanical properties, striae distensae fibroblasts appear as a different population from normal fibroblasts.

Adult↗
PubMed1999

Structural and immunohistological modifications in olfactory bulb of the staggerer mutant mouse.

In the present study, we describe the structural and cytological changes observed in staggerer mutant olfactory bulbs, as compared to normal mice. On the basis of photonic and ultrastructural observations we tried to define the alterations induced by the mutation: i.e. a reduction of bulb size, a reduction in the volume of three out of the six architectonic layers (glomerular, external and internal plexiform), a reduction of glomeruli size, a loss of half the mitral cells and a slight decrease in juxtaglomerular interneuron number. In staggerer, an hypertrophy of glial ensheathing cell processes was especially evident at the level of each glomerulus, whereas the density of the astrocyte network was weaker in the granular layer and the nerve layer not apparently impaired. An immunofluorescent labelling study combined with confocal scanning microscopy was performed in order to identify the cellular type and the differentiation degree of the various elements. Antibodies anti-GFAP, a protein present in both ensheathing cells and astrocytes, and anti-OMP, the specific maturation protein of the nerve layer, were used for that purpose. Data confirmed the reality of the gliosis and the persistence of the sensory component in the mutant. All the structural alterations described in staggerer olfactory bulb were in close agreement with the functional troubles previously recorded. Our results are discussed in connection with the present knowledge on embryonal origin, fetal development and adult cellular renewal of the olfactory bulb.

Animals↗
PubMed1997

Peroxisome proliferation and beta-oxidation in Fao and MH1C1 rat hepatoma cells, HepG2 human hepatoblastoma cells and cultured human hepatocytes: effect of ciprofibrate.

Human HepG2, rat Fao and MH1C1 hepatoma cell lines have been examined for their response to ciprofibrate, a potent peroxisome proliferator. Changes in the morphological characteristics of peroxisomes, the inductibility of their proliferation and of their beta-oxidation enzymes, palmitoyl-CoA oxidase and bifunctional enzyme, were studied in control and treated cells. In Fao cells, peroxisomes are less numerous and smaller than in rat liver, but they increase in size and number under the effect of ciprofibrate, similarly to those of treated rat liver. The high peroxisome proliferation is accompanied by a strong induction of beta-oxidation enzymes as in vivo. In MH1C1 cells, peroxisomes are seen in irregular clusters in the cytoplasm, small with rounded to tubular forms, suggesting rapid peroxisomal growth. A striking observation is the particularly elongated, worm-like form of many of the peroxisomes. Under the effect of ciprofibrate, the proliferation is low, as is the induction of beta-oxidation enzymes. HepG2 cells contain few, small peroxisomes with a heterogeneity of forms, from spherical to elongated. The only peroxisomal response to ciprofibrate in these cells seemed to be a morphological reorganization. There is little or no induction of beta-oxidation enzymes by ciprofibrate in HepG2 cells, as in cultured human hepatocytes. Therefore, on the one hand, Fao and MH1C1 cells are complementary tools in the investigation of the regulation of the hepatic response to peroxisome proliferators in the rat, on the other hand, HepG2 and Fao cells are useful in the study of the species specificity of the response.

3-Hydroxyacyl CoA Dehydrogenases↗
PubMed1995

In vitro effect of the gonad of Helix aspersa (Mollusca) on galactogen synthesis in the albumen gland of either mated or virgin snails.

The gonad of Helix aspersa contains a factor which can stimulate in a dose-dependent manner galactogen synthesis in albumen gland explants cultured in vitro. The stimulatory activity appears to be greater when the gonad is predominantly male than when it is predominantly female. The albumen gland of virgin snails does not respond in vitro to the gonadal influence. The receptivity of the albumen gland to the galactogen synthesis stimulating effect of the gonad is increased after the first and second mating. It decreases at the third mating in correlation with the increase of the albumen gland maturation index.

Animals↗
PubMed1992

Immunocytochemical localization of insulin-related peptide(s) in the central nervous system of the snail Helix aspersa Müller: involvement in growth control.

1. The presence of insulin-like substances has been demonstrated by immunocytochemistry in the central nervous system of the snail Helix aspersa. 2. The immunopositivity has been observed especially in the large perikarya of the mesocerebral green cells [the cerebral green cells (CeGC) stained in green by the alcian blue:alcian yellow technique]. 3. The removal of either the mesocerebrum or the CeGC stops the growth of the snail and induces the increase of the glycogen content in the mantle edge. 4. Our results show the existence of insulin-like material in the neurosecretory cells. Previous data having demonstrated the presence of specific binding sites to insulin in the cephalic ganglia of Helix aspersa, one may suggest that insulin could play a neuromodulatory or a neurotransmittory role in the central nervous system and might control the growth.

Animals↗
PubMed1992

Serum-free culture of stromal and functionally polarized epithelial cells of guinea-pig endometrium: a potential model for the study of epithelial-stromal paracrine interactions.

Stromal and glandular epithelial (GE) cells were isolated from guinea-pig endometrium and growth to near confluency (6-8 days) in primary culture on plastic surfaces in a serum-supplemented medium (SSM). The stromal cells were subcultured on plastic dishes and maintained for 72 h in SSM. Then SSM was replaced by a chemically defined medium (CDM) and the stromal cells grown to confluency (5-7 days). The GE cells were subcultured in CDM, on a basement membrane matrix (Matrigel) applied to permeable Millicell-PC filters, and grown to confluency (5 days). Homogeneity of the subcultured endometrial cell populations was ascertained immunocytochemically. The filter-cultured GE monolayers were polarized morphologically, and displayed epithelial-specific specialized structures. These monolayers had functional tight junctions as verified by a measurable transepithelial resistance. The subcultured cell populations were distinguished by an analysis of their cellular and secretory proteins after labelling with [35S]-methionine and analysis by polyacrylamide gel electrophoresis. The filter-cultured GE monolayers allowed identification of the proteins released vectorially in the apical or the basal secretory compartment, thus demonstrating the functional polarization of GE cells in this bicameral culture system. Within the defined conditions of this culture system, the paracrine factors released by the two endometrial cell populations as well as the interplay of stromal-epithelial interactions and ovarian hormones could be investigated.

Animals↗
PubMed1992

Progesterone control of fibronectin secretion in guinea pig endometrium.

Immunohistochemistry with a polyclonal antibody raised against human plasma fibronectin (Fn) was used to determine the localization of Fn in endometrial sections of guinea pig uteri isolated at the first, fourth, sixth, or tenth day of the estrous cycle. Immunoreactive Fn was constantly visualized in the endometrial stroma but absent from the epithelial layer. Fn was detected in the uterine lumen on the first or fourth day of the estrous cycle and was absent from the other sections. To determine the origin of this luminal Fn the ability of subcultured endometrial cells to produce Fn was tested, and the hormonal regulation of Fn secretion was studied. Cells were treated by estradiol alone or in association with progesterone, progesterone alone, or untreated. Whatever the hormonal treatment, stromal cells constantly secreted immunoreactive Fn into the culture medium. In the same way, the amount of Fn synthesized and basally secreted by epithelial cells was not affected by any hormonal treatments. However, Fn was found in the apical secretions of the untreated or estradiol-treated epithelial cells but was undetectable in the apical compartment when the epithelial cells were treated by progesterone alone or in association with estradiol. These results indicate that Fn is constitutively secreted by stromal cells and that subcultured epithelial cells of guinea pig endometrium secrete Fn from both their basal and apical membrane domains. However, the apical secretion of Fn is specifically suppressed by progesterone.

Animals↗
PubMed1991

[Asynchronous development of the genital tract in the snail, Helix aspersa, during growth and reproduction].

During the growth of laboratory-raised Helix aspersa, the development of the albumen gland and spermoviduct was studied in relation to age, weight and different stages of reproduction such as mating and egg-laying. The results showed that the population can be divided into 2 categories because of different growth rates and asynchronous development of the genital tract. The fast-growing snails are larger and reach sexual maturity (female type maturity) in a shorter period than slow growing snails (male type maturity). During growth, the maturation of the genital tract was not directly proportional to the weight of the animal. Within each class of similar weight and age of population, 2 groups were identified; in one group, the genital tract was significantly less developed than in the other. This asynchrony of genital tract development could still be found between mating partners of the same weight, the genital tract could be 3 times smaller in one than in the other partner. However, this difference disappeared between mating and egg-laying. These observations suggest: that asynchronous development of the genital tract could be a strategy for the developing population of Helix aspersa; and that (a) mating factor(s) is (are) involved in the regulation of the growth and function of the genital tract.

Animals↗
PubMed1986

[Action of the extract from the optic tentacles of juvenile and adult snails on the in vivo development of the albumin gland of Helix aspersa].

Injected optic tentacle homogenates in Helix aspersa were shown to cause a decrease in growth rate and albumen gland development. The effects of optic tentacles removed from young animals and from adult animals were compared. In young animals, injections of adult optic tentacle homogenate resulted in a reduction in both growth rate and albumen gland weight. In older adult animals injected with adult optic tentacle homogenate, growth and albumen gland development decreased, but not to the same extent as in young animals. In contrast, the inhibitory effect of the young tentacle homogenate was inverted. The possible source of a tentacular factor is discussed in relation to its possible origin in other investigated pulmonates, and also the mechanism of the homogenates heterochronic action.

Aging↗
PubMed1984

[In vitro study of the influence of dorsal bodies on oogenesis in Helix aspersa Müll].

Infantile gonads of Helix aspersa were cultured in vitro for 13 days, alone, associated with dorsal bodies, or with cerebral ganglia (surrounded by connective tissue containing the dorsal bodies). The results demonstrate the stimulatory effect of the dorsal bodies on oocyte growth and suggest that the cerebral ganglia have an inhibitory influence on dorsal body activity and/or on oocyte development.

Animals↗
PubMed1981

[Histological and ultrastructural study of the gonad of Helix aspersa Müller at hatching].

The gonad of young Helix aspersa, studied by light and electron microscopy during the first post-hatching week, showed a compact structure. Eventually, a lumen appeared as the cells moved apart. The gonad was composed of stem and germinal cells. The latter cells were represented by primordial germ cells and oocytes. With our method of rearing, the female germinal line differentiated first.

Animals↗