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Pale vacuolated epithelial cells in epididymis of aflatoxin-treated mice
1Department of Animal Science, School of Life Sciences, Bharathidhasan University, Tiruchirappalli-620024, India.
Abstract:
The responses of the mouse epididymal epithelium to subchronic doses of aflatoxin B1 were investigated in a histological study. Either few and large or small and profuse vacuoles containing an amorphous to dense periodic acid-Schiff-positive material were observed in the epithelium of all the segments of the epididymis. Resin-embedded semi-thin sections and transmission electron microscopy indicated that these vacuoles were intracellular. The cells that contained these vacuoles were quite different in organization and electron density from the cell types already established in the epididymal epithelium and are designated as pale vacuolated epithelial cells. Owing to aflatoxin B1 toxicity, the apical membrane of some of the principal cells, either individually or in groups, disintegrated so that the principal cells released their contents into the lumen of the duct through development of a 'fistula'. Spermatozoa from the ductal lumen entered the principal cell fistula and reached the basal lamina. If extravasation of the spermatozoa via this route occurred, it would bring about an autoimmune response, leading to the formation of spermatic granulomas and the generation of anti-sperm antibodies. Extravasation of spermatozoa seems to be offset by the underlying basal cell, which is presumed to develop into a pale vacuolated epithelial cell to enclose the disintegrating principal cells and the spermatozoa arriving at the principal cell. Thus, the development of pale vacuolated epithelial cells may be a protective device preventing an autoimmune response to sperm antigens in the context of toxicant-induced degeneration of the principal cells of the epididymal epithelium.
Insights
Aflatoxin B1 causes vacuolated cells and cell disintegration in the mouse epididymis. These pale vacuolated epithelial cells may protect against autoimmune responses to sperm antigens.
Area of Science:
- Reproductive toxicology
- Histopathology
- Cell biology
Background:
- The epididymis is crucial for sperm maturation and storage.
- Toxicant-induced damage to the epididymis can impair fertility.
- Understanding cellular responses to toxins is vital for reproductive health.
Purpose of the Study:
- To investigate the histological effects of aflatoxin B1 on the mouse epididymal epithelium.
- To identify and characterize novel cell types induced by aflatoxin B1 exposure.
- To elucidate the protective mechanisms against toxicant-induced epididymal damage.
Main Methods:
- Subchronic administration of aflatoxin B1 to mice.
- Histological examination of epididymal tissues.
- Resin-embedded semi-thin sections and transmission electron microscopy.
Main Results:
- Aflatoxin B1 induced intracellular vacuoles in epididymal epithelial cells, forming pale vacuolated epithelial cells.
- Principal cells showed apical membrane disintegration, creating fistulas that allowed sperm to reach the basal lamina.
- Basal cells appeared to differentiate into pale vacuolated cells, potentially enclosing damaged cells and sperm.
Conclusions:
- Pale vacuolated epithelial cells are a novel cell type in the epididymis, induced by aflatoxin B1.
- The formation of pale vacuolated cells may represent a protective mechanism against autoimmune responses to sperm antigens.
- Aflatoxin B1 causes significant structural damage to the epididymal epithelium, highlighting its reproductive toxicity.

