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1.
Histol Histopathol ; 25(10): 1277-85, 2010 10.
Article in English | MEDLINE | ID: mdl-20712012

ABSTRACT

Mesenchymal stem cells are a virtually ubiquitous population of adult stem cells, able to differentiate into various tissue lineages. As they are multipotent and easy to grow in culture, they are at present considered very attractive candidates for tissue repair and gene therapy. With the exception of a few reports, mesenchymal stem cell morphology has been widely disregarded in the past years. In this paper we discuss the establishment of mesenchymal stem cell cultures from equine adipose tissue and describe their fine structure by transmission electron microscopy. The cultured cells revealed a fibroblastoid appearance and were characterized by an eccentric nucleus with multiple nucleoli, dense cytoplasm rich in ribosomes, a rough endoplasmic reticulum with dilated cisternae, elongated mitochondria and heterogeneous vacuolar inclusions. In addition, they were often interconnected by adhesion structures located on the cell body and on cytoplasmic processes contacting other cells. The features observed are evocative of an undifferentiated cellular phenotype and of an intense synthetic and metabolic activity.


Subject(s)
Adipose Tissue/ultrastructure , Cell Differentiation , Mesenchymal Stem Cells/ultrastructure , Adipogenesis , Adipose Tissue/cytology , Adipose Tissue/metabolism , Animals , Biomarkers/metabolism , Cell Shape , Cells, Cultured , Chondrogenesis , Horses , Mesenchymal Stem Cells/metabolism , Microscopy, Electron, Transmission , Osteogenesis , Phenotype
2.
Vet J ; 185(2): 228-30, 2010 Aug.
Article in English | MEDLINE | ID: mdl-19477664

ABSTRACT

This study characterised the composition of surface and secretion complex carbohydrates in the alimentary tract of organically and intensively housed chickens. Histochemical labelling was carried out on samples of oesophagus, glandular stomach and proximal duodenum using (1) alcian blue (AB) at pH 2.5 combined with neuraminidase digestion (Sial) with or without saponification (KOH), (2) AB at pH 1 and 0.5, (3) periodic acid-Schiff (PAS), (4) a combined AB-PAS stain, and (5) both low and high iron diamine stains combined with enzymatic treatments specific for glycosaminoglycans. Semi-quantitative scoring of the histochemical staining indicated abundant acidic sulfated glycoconjugates in each alimentary tract region, in addition to the presence of sialoglycoderivatives in the oesophagus. These complex carbohydrate components are likely to have various functions including the provision of a protective visco-elastic barrier and a role in the defence against specific pathogens. The findings provide a starting point for a more in-depth study of alimentary tract glycoconjugates in poultry.


Subject(s)
Chickens , Digestive System/chemistry , Glycosaminoglycans/analysis , Animals , Histocytochemistry , Hydrogen-Ion Concentration , Periodic Acid-Schiff Reaction/veterinary , Staining and Labeling/veterinary
3.
Res Vet Sci ; 86(2): 189-93, 2009 Apr.
Article in English | MEDLINE | ID: mdl-18707745

ABSTRACT

The aim of the present study was to investigate the presence and the distribution of cells containing orexin A and orexin type 2 receptor in the horse stomach and gut, by means of immunohistochemical techniques. Orexin A was identified in the stomach fundic and pyloric regions and in the duodenum. In the same stomach regions, a large subset of orexin A-positive cells also showed orexin type 2 receptor-like immunoreactivity. Moreover, in the duodenum, many of them, seemed to store serotonin. Characteristically, enteric neurons or ganglia also displayed orexin A and, sometimes, orexin type 2 receptor immunoreaction. Orexin A and orexin type 2 receptor immunoreactivity was also found in the nerve fibers in the enteric submucosal layer. Our results, together with data present in the literature, could contribute to the understanding of complex mechanisms regulating the horse gut functionality that are depending very likely on the consequence of the co-operation of both a central and a peripheral control.


Subject(s)
Gastrointestinal Tract/metabolism , Horses/metabolism , Intracellular Signaling Peptides and Proteins/metabolism , Neuropeptides/metabolism , Receptors, G-Protein-Coupled/metabolism , Receptors, Neuropeptide/metabolism , Animals , Female , Gastrointestinal Tract/cytology , Immunohistochemistry/veterinary , Male , Orexin Receptors , Orexins
4.
Histol Histopathol ; 23(8): 973-8, 2008 08.
Article in English | MEDLINE | ID: mdl-18498072

ABSTRACT

This study was performed to identify the equine respiratory tract areas which express the specific receptor for equine influenza virus; findings may be useful to provide new ways to treat the infectious disease. The present work aims to visualize in situ the presence of sialoderivatives in the horse respiratory tract in order to localize sialoderivatives acting as influenza virus receptors. To this purpose, nasal mucosae, trachea, bronchus and lung parenchyma were removed from 8 mature horses of both sexes. We performed sialic acid characterization by means of mild and strong periodate oxidation and saponification, combined with lectin histochemistry and sialidase digestion, in addition to the direct evidentiation of sialic acid residues. No differences were shown between sexes. Sialic acid residues are present in the nasal mucous cell secretion, where they are linked to galactose by means of alpha2-3 linkage and are mainly C9 acetylated, and in the nasal and tracheal epithelial lining, where they are represented by periodate labile residues (alpha2-3)- and/or (alpha2-6)- linked to galactose. Specific receptors for equine influenza viruses are present at the nasal and tracheal epithelial lining cell coat levels, and in some trachea epithelial cells, but the horse possesses a preventive defence, which consists of the secretion of a mucous layer at nasal level, which could specifically inactivate the hemagglutinins of equine influenza virus; in addition, it expresses other sialoreceptors which can mask the influenza specific ones.


Subject(s)
Influenza A Virus, H3N8 Subtype/metabolism , N-Acetylneuraminic Acid/metabolism , Orthomyxoviridae Infections/virology , Receptors, Cell Surface/metabolism , Receptors, Virus/metabolism , Respiratory Tract Infections/virology , Animals , Female , Horse Diseases , Horses , Immunoenzyme Techniques , Influenza A Virus, H3N8 Subtype/isolation & purification , Lectins/metabolism , Male
5.
Vet Dermatol ; 17(4): 244-51, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16827667

ABSTRACT

It is widely documented that a pool of multipotent stem cells located in humans and mice hair follicle outer root sheath (bulge region) is involved in the restoration of the whole follicular unit during each anagen phase. To the authors' knowledge, data regarding the location and characterization of hair follicle stem compartment in dogs have not been reported in the recent relevant literature. In this study, we investigated the haematopoietic stem and progenitor cell antigen CD34 as a marker of putative stem cells located in a bulge-like region of canine hair follicles. The presence of CD34 mRNA and glycoprotein was assessed on formalin-fixed, paraffin-embedded canine skin samples by in situ hybridization technique and by standard immunohistochemistry, respectively. A strong expression of CD34 mRNA and glycoprotein was observed in a well-defined area of the hair follicle isthmic region and appeared uniformly concentrated at the level of the basal layer of the outer root sheath. These findings provide compelling support to the hypothesis that in dogs, a subpopulation of basal keratinocytes located in the hair follicle isthmic region and characterized by the selective expression of CD34 is potentially associated with the stem cell compartment of this skin appendage.


Subject(s)
Antigens, CD34/analysis , Hair Follicle/cytology , Stem Cells/cytology , Animals , Biomarkers/analysis , Dogs , Female , Glycoproteins/analysis , Immunohistochemistry/veterinary , In Situ Hybridization/veterinary , Male , RNA, Messenger/analysis
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