Lee E Y, Lee T S, Baik S H, Cha C I
Department of Anatomy, College of Medicine, Chungbuk National University, Cheongju, Korea.
Int J Dev Neurosci. 1998 Feb;16(1):63-72. doi: 10.1016/s0736-5748(97)00040-3.
The postnatal development of somatostatin (SOM)- and neuropeptide Y (NPY)-immunoreactive (ir) neurons was examined in rat cerebral cortex, while considering their coexistence in cortical neurons. Using double immunohistochemical staining for SOM and NPY with diaminobenzidine and benzidine dihydrochloride as chromogens, we subdivided immunoreactive cells into double-labeled SOM/NPY-, SOM only-, and NPY only-ir neurons. SOM/NPY- and SOM only-ir neurons were detectable even at the day of birth, in contrast on NPY only-ir cells which first appeared in most cortices from week two. The morphological features of double-labeled SOM/NPY neurons differed with those of SOM only- and NPY only-ir neurons. No apparent changes in the shape and size of single-labeled neurons occurred with age; throughout their postnatal life they were round and ovoid, had a thin rim of perinuclear cytoplasm, and short processes. However, the features of SOM/NPY-ir neurons were not consistent according to postnatal age; by day P7, these neurons showed immature features and they began to show more advanced neuronal characteristics by week P2, when they had a larger and more intensely-stain cytoplasm. In addition, their processes were longer, thicker and more complex than at earlier ages. At this age, SOM/NPY-ir somata were close to their near maximum size. From week P4, they became smaller and were lightly labeled. SOM/NPY-ir somata were larger than SOM only- and NYP only-ir somata at and after two weeks of age. The present results, showing different postnatal maturation patterns such as time of appearance and morphological features, raise the possibilities that double-labeled SOM/NPY and single-labeled immunoreactive neurons may be different populations regulated by different mechanisms in their development, and with different functional properties during development.
在考虑生长抑素(SOM)和神经肽Y(NPY)免疫反应性(ir)神经元在皮质神经元中共存的情况下,研究了大鼠大脑皮质中SOM和NPY免疫反应性神经元的出生后发育情况。使用以二氨基联苯胺和盐酸联苯胺作为显色剂对SOM和NPY进行双重免疫组织化学染色,我们将免疫反应性细胞细分为双重标记的SOM/NPY、仅SOM和仅NPY免疫反应性神经元。即使在出生当天也能检测到SOM/NPY和仅SOM免疫反应性神经元,相比之下,仅NPY免疫反应性细胞最早在第二周出现在大多数皮质中。双重标记的SOM/NPY神经元的形态特征与仅SOM和仅NPY免疫反应性神经元不同。单标记神经元的形状和大小不会随年龄发生明显变化;在它们的整个出生后生命中,它们呈圆形和椭圆形,有一层薄的核周细胞质边缘,且突起较短。然而,SOM/NPY免疫反应性神经元按出生后年龄的特征并不一致;在出生后第7天,这些神经元表现出不成熟的特征,到出生后第2周时开始表现出更成熟的神经元特征,此时它们有更大且染色更强烈的细胞质。此外,它们的突起比早期更长、更粗且更复杂。在这个年龄,SOM/NPY免疫反应性胞体接近其最大尺寸。从出生后第4周开始,它们变小且标记较浅。出生后两周及之后,SOM/NPY免疫反应性胞体比仅SOM和仅NPY免疫反应性胞体更大。目前的结果显示出不同的出生后成熟模式,如出现时间和形态特征,这增加了以下可能性:双重标记的SOM/NPY和单标记免疫反应性神经元可能是不同的群体,在其发育过程中受不同机制调控,并且在发育过程中具有不同的功能特性。