Naegele J R, Barnstable C J, Wahle P R
Department of Ophthalmology and Visual Sciences, Yale University School of Medicine, New Haven, CT 06510.
Proc Natl Acad Sci U S A. 1991 Jan 15;88(2):330-4. doi: 10.1073/pnas.88.2.330.
In the mammalian cerebral cortex, neurons destined for layers 2-6 are generated only after the period of genesis for a group of transient neurons that populate the subplate and marginal zones. Although a number of molecular markers for the subplate zone exist, most are also expressed by other cell populations in the cortical plate. To begin to study molecular properties of the subplate, we generated monoclonal antibodies against homogenates of cat cortical subplate zone. One monoclonal antibody, termed subplate 1 (SP1), recognized a polypeptide of 56 kDa. This antigen was strongly expressed within the subplate neurons only during a 3-week period beginning at birth and extending until 3 weeks after birth. From postnatal day 1, the number of SP1-immunoreactive neurons below the visual cortex increased until the end of second postnatal week and then declined thereafter. This period coincides with the period when a majority of the subplate neurons undergo naturally occurring cell death. The antigen was not expressed by subplate neurons surviving in the adult white matter. At the peak of antigen expression, 14% or less of the immunoreactive neurons also coexpressed gamma-aminobutyric acid, somatostatin, or neuropeptide Y. Biochemical and immunocytochemical properties of the SP1 antigen were also compared with the Alz-50 antigen (A68), a marker for dying neurons. On Western blots, SP1- and Alz-50-reactive polypeptides were selectively enriched in cytosolic fractions of kitten cerebral cortex, but each marker recognized different molecular weight polypeptides. In tissue sections many subplate, cortical plate, and layer 1 neurons were Alz-50 immunoreactive. In contrast, a rarer subpopulation of neurons restricted to the subplate was labeled by SP1. We propose that the SP1 antigen is a protein expressed within dying cortical subplate neurons, at the commencement of cell death.
在哺乳动物的大脑皮层中,注定要进入第2 - 6层的神经元仅在一群占据亚板层和边缘区的瞬时神经元的发生期之后产生。尽管存在许多亚板层区的分子标记,但大多数也在皮质板的其他细胞群体中表达。为了开始研究亚板层的分子特性,我们针对猫皮质亚板层区的匀浆产生了单克隆抗体。一种单克隆抗体,称为亚板层1(SP1),识别出一条56 kDa的多肽。这种抗原仅在出生后开始的3周内,即在出生后持续到出生后3周的时间内,在亚板层神经元中强烈表达。从出生后第1天开始,视皮层下方SP1免疫反应性神经元的数量在出生后第二周结束前增加,此后减少。这个时期与大多数亚板层神经元自然发生细胞死亡的时期相吻合。该抗原在成年白质中存活的亚板层神经元中不表达。在抗原表达的高峰期,14%或更少的免疫反应性神经元也共表达γ-氨基丁酸、生长抑素或神经肽Y。还将SP1抗原的生化和免疫细胞化学特性与Alz - 50抗原(A68)进行了比较,Alz - 50抗原是死亡神经元的标志物。在蛋白质免疫印迹法中,SP1和Alz - 50反应性多肽在小猫大脑皮层的胞质部分中选择性富集,但每个标志物识别不同分子量的多肽。在组织切片中,许多亚板层、皮质板和第1层神经元是Alz - 50免疫反应性的。相比之下,仅限于亚板层的较罕见的神经元亚群被SP1标记。我们提出,SP1抗原是一种在皮质亚板层神经元死亡开始时在其中表达的蛋白质。