Guldenaar S E, Nicholson H D, McCabe J T
Department of Anatomy and Cell Biology, U.S.U.H.S., F.E. Hébert School of Medicine, Bethesda, Maryland 20814-4799.
Anat Rec. 1992 Aug;233(4):538-42. doi: 10.1002/ar.1092330407.
The cellular localization of uterine oxytocin binding sites in the rat was studied by means of in vitro receptor autoradiography. Using [tyrosyl-3,5-3H]oxytocin as ligand, binding sites were localized in tissue sections from uteri of estrous, mated, and artificially cervically stimulated rats (n = 4 per group), and specificity of binding was investigated by means of simultaneous incubations with oxytocin, [Gly4,Thr7]oxytocin and [Arg]vasopressin. A previously unidentified type of cell was densely labelled by tritiated oxytocin. The labelled cells were preferentially localized near the endomyometrial border and at the interface of the circular and longitudinal muscle layers. In addition, these cells were found in the muscle layers. The dense labelling of these cells, which did not constitute part of the endometrial epithelium or blood vessels, was abolished when oxytocin or [Arg]vasopressin, but not [Gly4,Thr7]oxytocin, was added to the incubation medium. Binding of the radioligand was also found on muscle cells of the circular and longitudinal layers of the myometrium and cells of the endometrial luminal and glandular epithelium. Whereas incubation with oxytocin and [Gly4,Thr7]oxytocin diminished the labelling in both myometrium and endometrium, incubation with [Arg]vasopressin reduced labelling only in the myometrium. Similar results were obtained in tissues from rats in different reproductive states. This study demonstrates the presence of oxytocin binding sites in three different types of cell in the uterus of the rat. While the sites in the myometrium may be associated with the contractile response of this type of tissue to oxytocin, the functional significance of oxytocin binding sites on the endometrial epithelium and in the densely labelled, scattered cells remains to be elucidated.
通过体外受体放射自显影术研究了大鼠子宫催产素结合位点的细胞定位。使用[酪氨酸-3,5-³H]催产素作为配体,在动情期、交配后及人工刺激宫颈的大鼠子宫组织切片中定位结合位点(每组n = 4),并通过与催产素、[甘氨酸⁴,苏氨酸⁷]催产素和[精氨酸]加压素同时孵育来研究结合的特异性。一种先前未鉴定的细胞类型被氚标记的催产素密集标记。标记细胞优先定位于内膜肌层边界附近以及环形肌层和纵行肌层的交界处。此外,这些细胞也存在于肌层中。当向孵育培养基中添加催产素或[精氨酸]加压素而非[甘氨酸⁴,苏氨酸⁷]催产素时,这些并非子宫内膜上皮或血管组成部分的细胞的密集标记被消除。放射性配体的结合也见于子宫肌层环形和纵行层的肌细胞以及子宫内膜腔上皮和腺上皮细胞。虽然与催产素和[甘氨酸⁴,苏氨酸⁷]催产素孵育会减少子宫肌层和子宫内膜中的标记,但与[精氨酸]加压素孵育仅减少子宫肌层中的标记。在处于不同生殖状态的大鼠组织中获得了类似结果。本研究证明大鼠子宫中三种不同类型的细胞存在催产素结合位点。虽然子宫肌层中的位点可能与该类型组织对催产素的收缩反应有关,但催产素结合位点在子宫内膜上皮和密集标记的散在细胞上的功能意义仍有待阐明。