Department of Ecology and Evolutionary Biology, Yale University, New Haven, Connecticut, United States of America.
PLoS One. 2013 Aug 14;8(8):e72221. doi: 10.1371/journal.pone.0072221. eCollection 2013.
The muscular anatomy of the athecate hydroid Podocoryna carnea hydrorhiza is elucidated. The polyp-stolon junction is characterized by an opening, here called the chloe, in the otherwise continuous hydrorhizal perisarc. The chloe is elliptical when the polyp first arises, but takes on a more complex outline as multiple stolons anastomose to communicate with that polyp. Surrounding the polyp base are spots, here called anchors, which autofluoresce at the same wavelengths as perisarc and which, like perisarc, contain chitin as assessed by Calcofluor White, Congo Red and wheat germ agglutinin staining. Anchors remain after living tissues are digested using KOH. Collagen IV staining indicates that the mesoglea is pegged to the anchors and rhodamine phallodin staining detects cytoskeletal F-actin fibers of the basal epidermis surrounding the anchors. Longitudinal muscle fibers of the polyp broaden at the polyp base and are inserted into the mesoglea of the underlying stolon, but were neither observed to extend along the stolonal axis nor to attach to the anchors. Circular muscular fibers of the polyp extend into stolons as a dense collection of strands running along the proximal-distal axis of the stolon. These gastrodermal axial muscular fibers extend to the stolon tip. Epidermal cells at the stolon tip and the polyp bud display a regular apical latticework of F-actin staining. A similar meshwork of F-actin staining was found in the extreme basal epidermis of all stolons. Immunohistochemical staining for tubulin revealed nerves at stolon tips, but at no other hydrorhizal locations. These studies bear on the mechanisms by which the stolon tip and polyp bud pulsate, the manner in which the stolon lumen closes, and on the developmental origin of the basal epidermis of the hydrorhiza.
阐明了无鞘水母 Podocoryna carnea hydrorhiza 的肌肉解剖结构。珊瑚虫茎节连接处有一个开口,这里称为“chloe”,在无鞘的水螅体被膜的连续部分中形成开口。当珊瑚虫最初出现时,chloe 呈椭圆形,但随着多个茎节吻合以与该珊瑚虫沟通,chloe 会呈现出更复杂的轮廓。围绕珊瑚虫基部的是斑点,这里称为“锚”,这些锚在与被膜相同的波长处自发荧光,并且与被膜一样,在用 KOH 消化活组织后仍然存在,用 Calcofluor White、刚果红和麦胚凝集素染色评估含有几丁质。胶原 IV 染色表明中胶层被固定在锚上,罗丹明鬼笔环肽染色检测围绕锚的基表皮的细胞骨架 F-肌动蛋白纤维。珊瑚虫的纵向肌肉纤维在珊瑚虫基部变宽,并插入到下面茎节的中胶层中,但既未观察到它们沿茎节轴延伸,也未观察到它们附着在锚上。珊瑚虫的圆形肌肉纤维延伸到茎节中,形成沿着茎节近-远轴的密集链。这些腹侧轴向肌肉纤维延伸到茎节末端。茎节末端和珊瑚虫芽的表皮细胞显示出 F-肌动蛋白染色的规则顶端格子结构。在所有茎节的极端基表皮中都发现了类似的 F-肌动蛋白染色网格。微管蛋白免疫组织化学染色显示在茎节末端有神经,但在水螅体的其他位置没有。这些研究涉及茎节末端和珊瑚虫芽跳动的机制、茎节腔关闭的方式以及水螅体基表皮的发育起源。