Brennan E M, Martin L J, Johnston M V, Blue M E
The Kennedy Krieger Research Institute, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
J Comp Neurol. 1997 Sep 15;386(1):29-45. doi: 10.1002/(sici)1096-9861(19970915)386:1<29::aid-cne5>3.0.co;2-f.
The ontogeny of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) and kainate (KA) glutamate receptors in rat barrel field cortex was characterized by using receptor autoradiography and immunocytochemistry. A somatotopic pattern of AMPA receptors with fewer [3H]AMPA sites in barrel centers than in surrounding cortex did not emerge until postnatal day 10 (P10). After reaching a peak density at P14, the density of [3H]AMPA receptors declined in both barrel centers and surrounding cortex. Compared with AMPA receptors, the density of [3H]KA sites at all ages was low, a somatotopic expression of [3H]KA sites was missing, and the developmental curve for [3H]KA sites was more shallow than that for [3H]AMPA binding sites. A differential ontogeny of AMPA and KA receptors in barrel field cortex was also demonstrated in immunocytochemical studies with antibodies to the AMPA receptor subunits GluR1 and GluR2,3 and the KA receptor subunits GluR6,7. GluR1 and GluR2,3 staining was more dense in barrel septa than in barrel centers; this pattern persisted into adulthood. GluR1 and GluR2,3 receptors were localized to cell bodies and dendrites as well as the neuropil, but different populations of cortical neurons expressed these receptors. At P10, KA receptor subunits GluR6,7 exhibited a contrasting pattern to that of AMPA receptor subunits, with slightly more neuropil staining in barrel centers than in surrounding cortex. After that point, the somatotopic pattern of GluR6,7 subunit expression was lost. The contrasting developmental patterns of expression of the AMPA and KA receptors in the barrel field suggest that they may play different roles in the whisker-to-barrel pathway.
运用受体放射自显影术和免疫细胞化学方法,对大鼠桶状皮质中α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)和海人藻酸(KA)谷氨酸受体的个体发生进行了表征。直到出生后第10天(P10),AMPA受体的躯体定位模式才出现,即桶状中心的[3H]AMPA位点比周围皮质少。在P14达到峰值密度后,[3H]AMPA受体的密度在桶状中心和周围皮质均下降。与AMPA受体相比,各年龄段的[3H]KA位点密度较低,[3H]KA位点不存在躯体定位表达,且[3H]KA位点的发育曲线比[3H]AMPA结合位点的发育曲线更平缓。在使用针对AMPA受体亚基GluR1和GluR2,3以及KA受体亚基GluR6,7的抗体进行的免疫细胞化学研究中,也证实了桶状皮质中AMPA和KA受体的个体发生存在差异。GluR1和GluR2,3在桶状间隔中的染色比在桶状中心更密集;这种模式持续到成年期。GluR1和GluR2,3受体定位于细胞体、树突以及神经毡,但不同群体的皮质神经元表达这些受体。在P10时,KA受体亚基GluR6,7表现出与AMPA受体亚基相反的模式,桶状中心的神经毡染色略多于周围皮质。此后,GluR6,7亚基表达的躯体定位模式消失。桶状皮质中AMPA和KA受体表达的不同发育模式表明,它们可能在触须到桶状通路中发挥不同作用。