Abstract
This study identified the cellular compositions of the gills in molly fish and their role in immunity using light-, electron- microscopy, and immunohistochemistry. The molly fish gills consisted of four holobranchs spaced between five branchial slits. Each hemibranch carried many fine primary and secondary gill lamellae. The gill arch was a curved cartilaginous structure, from which radiated the bony supports of the primary lamellae. The gill arch contained the afferent and efferent brachial arteries. The gill arch was covered by epidermal tissue rich with mucous cells. The primary lamella had a central cartilaginous support and efferent and afferent arterioles and was covered with pavement cells (PVC), salt-secreting chloride cells, and pale-staining mucous cells. These chloride cells contained abundant mitochondria and tubulovesicular system and are involved in ionic transport with a potential role in detoxification. The surface of the secondary lamellae (site of gaseous exchange) consisted of overlapping or interdigitating PVC supported and separated by pillar cells. Other cells were found within the gill epithelium and interstitial connective tissues, including lymphocytes, macrophages, monocytes, telocytes, stem cells, astrocytes, and neuroepithelial cells. The immunohistochemical analysis revealed that APG-5, iNOS-2, IL-1β, NF-κB, and TGF-B showed positive immunoreactivity in macrophages. The epithelium of the primary gill lamellae contained positive-GFAP astrocytes and S100 protein—chloride cells. The stem cells expressed SOX9, myostatin, and Nrf2. Neuroendocrine cells expressed S100 protein. In conclusion, the current work suggests that the gills of molly fish are multifunctional organs and are involved in immune reactions.
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