A prominent feature of disease induced by Mycoplasma gallisepticum is a lymphoproliferative response in the respiratory tract. Although this is also seen in other mycoplasma infections, including Mycoplasma pneumoniae, the phenotype of the lymphocytes infiltrating the respiratory tract has not been determined. In this study, the numbers and distribution of lymphocytes in the tracheas of chickens infected with a virulent strain of M. gallisepticum were examined. Three groups of chickens were experimentally infected with M. gallisepticum and three unchallenged groups were used as controls. One infected and one control group were culled at 1, 2 and 3 weeks post infection.
Changes in the ovine mammary gland epithelium during initiated involution were studied by light and electron microscopy. Apoptosis of the duct and alveolar epithelial cells was first identified at 2 d after weaning, reached a peak at 4 d and then progressed gradually thereafter. Apoptotic cells were phagocytosed by intraepithelial macrophages and alveolar epithelial cells. Occasional apoptotic epithelial cells were observed in the alveolar and duct lumina. The highly vacuolated cells in the alveolar and duct lumina were confirmed to be macrophages as they were CD45+, MHC class II+. Changes in myoepithelial cells involved shrinkage and extension of cytoplasmic processes into the underlying stroma and no apoptosis was observed. Regression of the blood capillaries was also by apoptosis. The resulting apoptotic bodies were either taken up by adjacent endothelial cells or were shed into the capillary lumen to be phagocytosed later by mural endothelial cells or blood monocytes. The mammary glands were completely involuted by 30 d after weaning. It was concluded that the mammary gland involutes by apoptosis, a process which allows deletion of cells without the loss of the basic architecture and the integrity of the epithelial lining of the gland.
Mammary glandular tissues and mammary secretions were obtained from sheep at 2-60 d after weaning to study the leucocyte phenotypes associated with mammary involution. From 2-4 d after weaning, neutrophils were the predominant leucocytes in the alveolar and ductal lumina. Lymphocytes were present in the alveolar and ductal epithelium, interalveolar and periductal areas. Most of the lymphocytes in the alveolar and ductal epithelium (IEL) were CD8 + , some were CD45R + and few were CD4 + . In the periductal clusters and in the interalveolar areas most of the lymphocytes were CD4 + . There was a significant increase (P 0n05) in the percentages of CD45R + granulated IEL from 2 to 7 d after weaning, and this paralleled the increase in the percentages of apoptotic cells in the glandular epithelium. By 7-60 d after weaning, most cells within the alveolar and ductal lumina were macrophages followed by predominantly CD8 + lymphocytes. CD8 + lymphocytes were still predominant in the alveolar and ductal epithelium while CD4 + cells were predominant in the interalveolar areas. Very few γδ + T cells were observed at all the stages examined. The cells in the mammary secretions correlated with those observed in the alveolar and ductal lumina. At the early stages of involution, the neutrophils and macrophages were heavily laden with lipid droplets, casein and cellular debris. The most interesting feature was the presence of cells either with extensive cytoplasmic processes (LCA + MHC class II + ) or cytoplasmic veils (LCA + MHC class II + CD1 + ), probably dendritic cells. It is concluded that the cellular constituents of the mammary gland at the latter part of involution may afford the mammary gland more resistance to infection than the lactating gland and the gland at early stages of involution. The CD45R + IEL may trigger apoptotic cell death in the mammary glandular epithelium during mammary involution.Key words : Lactation ; granulated lymphocytes ; mammary regression ; dendritic cells. It has been reported that the early period of mammary gland involution coincides with a period of acutely increased susceptibility to intramammary infection (Nickerson, 1989 ;Oliver & Sordillo, 1989). One of the reasons given was that this could be due to the loss of the physical barrier by sloughing of the alveolar epithelium. Our recent studies (Lee et al. 1996 ;Tatarczuch et al. 1997) excluded this possibility as it was clearly shown that the process of apoptosis enabled the deletion of the alveolar epithelial cells without the loss of the integrity of the epithelial lining of the gland.Our previous studies (Lee et al. 1989) showed thatCorrespondence to Dr C. S. Lee, Department of Veterinary Science, The University of Melbourne, 3010, Victoria, Australia. Fax :j61 3 9344 7374 ; e-mail : c.lee!vet.unimelb.edu.au in the mammary gland of both nonpregnant and pregnant sheep, the great majority of the lymphocytes in the ductal and alveolar epithelium were agranulated and that they belong to the CD8 + CD5 V phenotype follow...
There are many reports describing fractures in the bony elements of the equine fetlock joint and a few of these discuss possible relationships of these fractures to the mechanical loading of these bones. The likelihood of fracture must be related to the size and shape of bones involved, but information concerning the normal range in size and shape of these bones in horses is lacking. This study aimed to identify morphometrical variations of these bones within different groups of horses. Right and left metacarpal, proximal phalangeal and proximal sesamoid bones were collected from 10 Thoroughbreds (TB), five Standardbreds (SB) and eight Ponies (P) euthanized for non-orthopaedic reasons. All bones were boiled, cleaned and dried. Dimensional parameters were measured using a custom-built apparatus, calliper and plastic tape. The width and depth of the medial condyles of Mc3 were greater than the lateral condyles in all groups. The length to the lateral condyle was greater than the length to the medial condyle of Mc3, and the lengths of the lateral sides of the Mc3 and P1 bones were greater than the lengths of the medial sides in both forelimbs of all groups. The lateral sesamoids were similar to, or larger than, the medial sesamoids in all dimensions. There were some morphometrical variations in the bony elements of the equine fetlock joints in all groups.
Lactating animals are particularly susceptible to mastitis during the early stages of mammary gland involution following weaning. In this study we compared the phagocytic capacity of cells collected from sheep mammary secretions at different stages of involution. The ability of neutrophils and macrophages to ingest latex beads in an in vitro phagocytosis assay was found to be dependent on how heavily the phagocytes were loaded with milk constituents. There was a decline in the phagocytic capacity of neutrophils from 1 to 2 days after weaning, while macrophages collected from fully involuted glands were more effective phagocytes compared with earlier stages (7-15 days) of involution. In addition, dendritic cells present in fully involuted mammary gland secretions (30 days after weaning) were highly phagocytic. These studies demonstrate that neutrophils and macrophages in sheep mammary secretions at early stages of involution are incapacitated, and as such may compromise the immune status of the mammary gland.
Sacrocaudal fusion appears to be more prevalent in Greyhounds than in other domestic dog breeds and may be attributable to selection pressure for speed on a region of the spine that is naturally prone to variation. Its significance for performance and soundness requires further study.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.