Dutton J L, Hansen M A, Balcar V J, Barden J A, Bennett M R
Department of Physiology, The University of Sydney, NSW 2006, Australia.
J Neurocytol. 1999 Jan;28(1):4-16. doi: 10.1023/a:1007043132537.
Postnatal development of the distribution of different isoforms of purinergic (P2X) receptors on smooth muscle cells in relation to the development of the innervation of the cells by nerve varicosities in the rat urinary bladder has been determined with immunofluorescence and confocal microscopy. Antibodies against the extracellular domains of the P2X(1) to P2X(6) receptors were used to detect the receptors in the bladder. Several other antibodies were used to identify sympathetic varicosities and Schwann cells. At one day postnatal (D1) there were few strings of varicosities denoting isolated axons, with most axons confined to large nerve trunks. Small size clusters of P2X(1) to P2X(6) receptor subtypes (about 0.4 microm diameter) were observed in the muscle which were independent of each other, and sometimes juxtaposed to the rare isolated varicosity strings. At D4 large numbers of strings of varicosities could be discerned throughout the detrusor. Most of these clouds of small P2X(1) to P2X(6) receptor clusters in their immediate vicinity. Some of these were colocalised with the varicosities, which were of parasympathetic origin as they failed to counter-stain with antibodies to tyrosine hydroxylase. Up to D14 there was a gradual coalescence of many of the isolated P2X(1-6) small receptor clusters so that they became colocalized, often at varicosities. Most of the varicosities in isolated strings possessed receptor clusters at this time. By D21 it was rare to find varicosity strings in the detrusor that were not either in close juxtaposition with P2X small receptor clusters or possessing such clusters in colocalization. However, large numbers of small P2X receptor clusters, many of which consisted of a mixture of isoforms, could be found spatially unrelated to nerve varicosities throughout the detrusor muscle. In the adult, single axons were either coextensive with one or more isoforms of P2X receptor clusters or these were immediately juxtaposed to the axons so that is was rare to find a varicosity that did not possess a receptor cluster. However, different combinations of colocalized P2X receptor isoforms could still be discerned in small clusters unrelated to varicosities. These observations are discussed in relation to the mechanism of formation of the receptor clusters and their migration beneath parasympathetic varicosities during development.
通过免疫荧光和共聚焦显微镜,已确定了大鼠膀胱中平滑肌细胞上嘌呤能(P2X)受体不同亚型分布的产后发育情况,及其与神经膨体对细胞支配发育的关系。使用针对P2X(1)至P2X(6)受体细胞外结构域的抗体来检测膀胱中的受体。还使用了其他几种抗体来识别交感神经膨体和雪旺细胞。出生后一天(D1),表示孤立轴突的膨体串很少,大多数轴突局限于大神经干。在肌肉中观察到P2X(1)至P2X(6)受体亚型的小尺寸簇(直径约0.4微米),它们彼此独立,有时与罕见的孤立膨体串并列。在D4时,整个逼尿肌中可以辨别出大量的膨体串。在它们的紧邻区域有大多数这些小的P2X(1)至P2X(6)受体簇云。其中一些与膨体共定位,这些膨体是副交感神经起源的,因为它们不能用酪氨酸羟化酶抗体进行复染。直到D14,许多孤立的P2X(1 - 6)小受体簇逐渐合并,从而它们常常在膨体处共定位。此时,孤立串中的大多数膨体都拥有受体簇。到D21时,在逼尿肌中很少发现不与P2X小受体簇紧密并列或不与之共定位的膨体串。然而,在整个逼尿肌中可以发现大量与神经膨体在空间上不相关的小P2X受体簇,其中许多由亚型混合物组成。在成体中,单个轴突要么与一种或多种P2X受体簇亚型共延,要么这些受体簇紧邻轴突,因此很少发现没有受体簇的膨体。然而,在与膨体无关的小簇中仍可辨别出共定位的P2X受体亚型的不同组合。结合受体簇的形成机制及其在发育过程中在副交感神经膨体下方的迁移对这些观察结果进行了讨论。