Canine Uterine Epithelial Cells

Cat.No.: CSC-C9131J

Species: Dog

Source: Uterus

Cell Type: Epithelial Cell

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Cat.No.
CSC-C9131J
Description
Canine Uterine Epithelial Cells from Creative Bioarray are isolated from uterine tissue of pathogen-free laboratory Canine. Canine Uterine Epithelial Cells are grown in a T25 tissue culture flask pre-coated with gelatin-based coating solution for 2 min and incubated in Creative Bioarray’s Culture Complete Growth Medium for 3-5 days. Prior to shipping, cells at passage 2 are detached from flasks and immediately cryo-preserved in vials. Each vial contains at least 0.5x10^6 cells per ml and is delivered frozen. Cells can be expanded for 3-7 passages at a split ratio of 1:2 under the cell culture conditions specified by Creative Bioarray. Repeated freezing and thawing of cells is not recommended.
Species
Dog
Source
Uterus
Recommended Medium
Complete Epithelial Cell Medium
Cell Type
Epithelial Cell
Disease
Normal
Storage and Shipping
We ship frozen cells on dry ice. Upon receiving, directly and immediately transfer the cells from dry ice to liquid nitrogen and keep the cells in liquid nitrogen until they are needed for experiments. Never can primary cells be kept at -20 °C.
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

Canine uterine epithelial cells are primary epithelial cells from the inner mucosal layer of the canine uterus and constitute an essential physiological and structural barrier in the female canine reproductive tract. This cell type mostly consists of endometrial luminal epithelial cells and glandular epithelial cells, which are critical for the maintenance of homeostasis of the uterine environment, embryo implantation, and gestational establishment.

They release cytokines, growth factors and uterine fluid components that affect maternal-fetal communication and immunological tolerance in pregnancy. Moreover, these cells are implicated in inflammatory responses and the pathological development of common canine reproductive illnesses, including pyometra, endometritis, and hormone-induced uterine lesions.

Canine uterine epithelial cells are widely used in in vitro experimental models to aid research in reproductive endocrinology, pathogen-host interaction, endometrial pathophysiology and drug screening for canine reproductive diseases, and also provide an important cellular tool for veterinary reproductive biology and preclinical studies.

Oleic Acid Induces Lipid Droplet Accumulation in Canine Endometrial Epithelial Cells

Recent observations of lipid droplet (LD) accumulation in pyometra-affected uteri prompted a comparison of LD localization, quality, and quantity in healthy versus diseased tissues and in vitro models.

Oil Red O (ORO) staining revealed that canine endometrial epithelial cells cultured without lipid supplementation contained few, homogeneously sized LDs. However, treatment with oleic acid-alone or with cholesterol-significantly increased LD accumulation (Fig. 1A). Cholesterol alone had no effect. Quantitative image analysis showed a significant rise in ORO-positive area in oleic acid-treated groups compared to controls (Fig. 1B), which was corroborated by spectrophotometry (2-3-fold increase, Fig. 1C).

Immunostaining for perilipin 2 (PLIN2) mirrored ORO results, confirming increased LDs with oleic acid ± cholesterol treatment (Fig. 1A, D). PLIN3 staining revealed a granular cytoplasmic pattern that shifted moderately with oleic acid treatment due to enlarged LDs (Fig. 1A). Quantification showed a significant increase in PLIN3 signal in oleic acid-treated groups (Fig. 1E). These data demonstrate that canine endometrial epithelial cells actively process exogenous fatty acids, leading to LD accumulation.

Lipid droplet dynamics in healthy and pyometra-affected canine endometrium.

Fig. 1. Lipid droplet dynamics in healthy and pyometra-affected canine endometrium (Leitner N, Hlavaty J, et al., 2022).

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