Abstract

BackgroundThe reproductive strategies of vertebrates are diverse. Seahorses (Pisces: Syngnathidae) possess the unique characteristic of male pregnancy; i.e., males, not females, incubate embryos in a specialized structure called a ‘brood pouch’. The brood pouch is formed along the ventral midline of the tail. The lumen of the brood pouch is surrounded by loose connective tissue, called pseudoplacenta, and dermis.ResultsWe visualized and evaluated the morphology of brood pouch formation in Hippocampus abdominalis to gain generalizable insights into this process in seahorses. First, we employed several staining methods to characterize the pseudoplacenta and dermis of the brood pouch of mature male seahorses. The pseudoplacenta is composed mainly of reticular fibers, while the dermis is composed mainly of collagenous fibers. Further observations showed that pouch formation is initiated by linear projections of epithelia on both ventrolateral sides of the body. These projections elongated toward the ventral midline, eventually fused together, and then formed a baggy structure composed of a single dermis layer with neither smooth muscle nor pseudoplacenta. Finally, the pseudoplacenta was formed, together with two layers of dermis and smooth muscle. Thus, a fully developed brood pouch was established. The morphology of the luminal epithelium also changed during pouch formation. We analyzed the localization of C-type lectins as markers; haCTL II was localized in both the outer and luminal epithelia of the brood pouch throughout development in the male seahorse, whereas haCTL IV, which was not detected in the early stage of seahorse development, became localized only in the luminal epithelium as development proceeded.ConclusionsWe categorized the processes of brood pouch formation during male seahorse development into three stages: (1) the early stage, characterized by formation of a baggy structure from the primordium; (2) the middle stage, characterized by the differentiation and establishment of brood pouch-specific tissues; and (3) the late stage, characterized by a fully formed pouch with developing blood vessels and a pouch fold ultimately capable of carrying and incubating embryos.

Highlights

  • The reproductive strategies of vertebrates are diverse

  • Some species of gobies and sticklebacks protect their eggs until hatching by making nests, and some species of cichlids protect eggs and hatched-out fry within their mouths [1]

  • Scale bars: a, h, l, p = 1 mm; b–g, i–k, m–o, and q–s = 20 μm. bv, blood vessel; le, luminal epithelium; mg, mucous granule; oe, outer epithelium; pg, pigment cell; pp, pseudoplacenta; sc, stratum compactum; sk, skeletal muscle; sm, smooth muscle; ss, stratum spongiosum. These photographs were taken using two individual male seahorses; one specimen for a, h, p, and another for l, due to the lack of black staining in the first specimen granules were found in the luminal epithelium (Fig. 1b)

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Summary

Methods

Fish Pot-bellied seahorses, Hippocampus abdominalis, aged 20–30 days (20 individuals), two months (two individuals), three months (one individual), five months (one individual), six months (one individual), seven months (three individuals), and eight months (two individuals), as well as several mature adults, were obtained from Seahorse Ways Co. Ltd., Kagoshima, Japan, for use in the present study. The samples were dehydrated in a stepwise manner using 25, 50, 70, 90, 95 and 100% ethanol, and embedded in paraffin following the standard protocol [17]. Thin (8-μm) sections were cut with a Microm HM 325 Rotary Microtome (Thermo ScientificTM), deparaffinized in Clear-Rite 3 (Thermo ScientificTM Richard-Allan ScientificTM), and stained using the standard protocols for hematoxylin and eosin stain, Masson’s trichrome stain, reticulin silver stain, and Elastica van Gieson stain [17]. The samples were observed under a light microscope (BX51, Olympus, Tokyo, Japan) equipped with a digital camera (D7000, Nikon, Tokyo, Japan)

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