Lavin S T, Southwell B R, Murphy R, Jenkinson K M, Furness J B
Department of Anatomy and Cell Biology, University of Melbourne, Parkville, Victoria, Australia.
Histochem Cell Biol. 1998 Sep;110(3):263-71. doi: 10.1007/s004180050288.
The aims of this work were to determine whether cells that are similar to the interstitial cells of Cajal (ICC) and have immunoreactivity for the neurokinin 1 (NK1) receptor are indeed ICC; to determine whether the agonist, substance P, binds to and activates the receptor on presumptive ICC; and to investigate the relationship between substance P-immunoreactive nerve fibres and ICC. ICC at the level of the myenteric plexus and in the deep muscular plexus in the duodenum and ileum of the guinea-pig were investigated. Immunoreactivities for the ICC marker, Kit, and the NK1 receptor were colocalised in ICC of the myenteric and deep muscular plexuses. In tissue fixed immediately after its removal from the animal, NK1 receptor-immunoreactive ICC were found at the level of the myenteric plexus in the duodenum, but not in the ileum, and in the deep muscular plexus in the duodenum and ileum. The majority of receptor immunoreactivity was on the cell surface. ICC were exposed to substance P (10(-7) M), initially at 4 degrees C for 1 h to allow the agonist to bind, followed by incubation at 37 degrees C to allow receptor internalisation to proceed. Exposure to substance P caused the NK1 receptor immunoreactivity to aggregate in clumps in the cytoplasm of ICC of the myenteric and deep muscular plexuses, including the ICC of the myenteric plexus of the ileum, where NK1 receptor immunoreactivity was not seen if tissue was not exposed to substance P. Substance P, to which the fluorescent label, cyanine 3.18 (Cy-3), was coupled, bound to the ICC. The Cy-3-substance P was internalised with the receptor following warming to 37 degrees C. Many, but not all, ICC were closely apposed by nerve fibres with immunoreactivity for substance P. It is concluded that the NK1 receptor immunoreactivity on ICC represents receptor that is functional in the sense that it binds the natural agonist substance P and undergoes agonist-induced internalisation. ICC are likely to receive excitatory innervation from the close approaches of tachykinin-containing nerve fibres.
这项工作的目的是确定那些类似于 Cajal 间质细胞(ICC)且对神经激肽 1(NK1)受体具有免疫反应性的细胞是否确实为 ICC;确定激动剂 P 物质是否与假定的 ICC 上的受体结合并激活该受体;以及研究 P 物质免疫反应性神经纤维与 ICC 之间的关系。对豚鼠十二指肠和回肠的肌间神经丛水平以及深部肌丛中的 ICC 进行了研究。ICC 标志物 Kit 和 NK1 受体的免疫反应性在肌间和深部肌丛的 ICC 中共定位。在从动物身上取出后立即固定的组织中,在十二指肠的肌间神经丛水平发现了 NK1 受体免疫反应性 ICC,但在回肠中未发现,在十二指肠和回肠的深部肌丛中也发现了。大多数受体免疫反应性位于细胞表面。将 ICC 暴露于 P 物质(10⁻⁷ M),最初在 4℃下放置 1 小时以使激动剂结合,然后在 37℃下孵育以使受体内化进行。暴露于 P 物质导致 NK1 受体免疫反应性在肌间和深部肌丛的 ICC 细胞质中聚集成团,包括回肠肌间神经丛的 ICC,在未暴露于 P 物质的组织中此处未见 NK1 受体免疫反应性。与荧光标记物花青素 3.18(Cy - 3)偶联的 P 物质与 ICC 结合。升温至 37℃后,Cy - 3 - P 物质与受体一起内化。许多(但不是全部)ICC 与对 P 物质具有免疫反应性的神经纤维紧密相邻。得出的结论是,ICC 上的 NK1 受体免疫反应性代表了一种功能性受体,因为它能结合天然激动剂 P 物质并经历激动剂诱导的内化。ICC 可能通过含速激肽神经纤维的紧密靠近而接受兴奋性神经支配。