Shetty Ashok K, Hattiangady Bharathi
Institute for Regenerative Medicine, Texas A&M Health Science Center College of Medicine at Scott & White, Temple, TX, USA; Research Service, Olin E. Teague Veterans' Medical Center, CTVHCS, Temple, TX, USA; Department of Molecular and Cellular Medicine, Texas A&M Health Science Center College of Medicine, College Station, TX, USA; Division of Neurosurgery, Duke University Medical Center, Durham, NC, USA; Research and Surgery Services, Durham Veterans Affairs Medical Center, Durham, NC, USA.
Int J Dev Neurosci. 2013 Nov;31(7):646-56. doi: 10.1016/j.ijdevneu.2013.05.006. Epub 2013 Jun 3.
While neural stem/progenitor cells (NSCs) in the dentate gyrus of the hippocampus have been extensively characterized, the behavior of NSCs in the CA1 and CA3 subfields of the hippocampus is mostly unclear. Therefore, we compared the in vitro behavior of NSCs expanded from the micro-dissected CA1 and CA3 subfields of postnatal day (PND) 4 and 12 Fischer 344 rats. A small fraction (∼1%) of dissociated cells from CA1 and CA3 subfields of both PND 4 and 12 hippocampi formed neurospheres in the presence of EGF and FGF-2. A vast majority of neurosphere cells expressed NSC markers such as nestin, Sox-2 and Musashi-1. Differentiation assays revealed the ability of these NSCs to give rise to neurons, astrocytes, and oligodendrocytes. Interestingly, the overall neuronal differentiation of NSCs from both subfields decreased with age (23-28% at PND4 to 5-10% at PND12) but the extent of oligodendrocyte differentiation from NSCs increased with age (24-32% at PND 4 to 45-55% at PND 12). Differentiation of NSCs into astrocytes was however unchanged (40-48%). Furthermore, NSCs from both subfields gave rise to GABA-ergic neurons including subclasses expressing markers such as calbindin, calretinin, neuropeptide Y and parvalbumin. However, the fraction of neurons that expressed GABA decreased between PND4 (59-67%) and PND 12 (25-38%). Additional analyses revealed the presence of proliferating NSC-like cells (i.e. cells expressing Ki-67 and Sox-2) in different strata of hippocampal CA1 and CA3 subfields of both PND4 and PND 12 animals. Thus, multipotent NSCs persist in both CA1 and CA3 subfields of the hippocampus in the postnatal period. Such NSCs also retain their ability to give rise to both GABA-ergic and non-GABA-ergic neurons. However, their overall neurogenic potential declines considerably in the early postnatal period.
虽然海马齿状回中的神经干/祖细胞(NSCs)已得到广泛研究,但海马CA1和CA3亚区中NSCs的行为大多仍不清楚。因此,我们比较了从出生后第4天和第12天的Fischer 344大鼠的显微解剖CA1和CA3亚区扩增出的NSCs的体外行为。在表皮生长因子(EGF)和碱性成纤维细胞生长因子-2(FGF-2)存在的情况下,出生后第4天和第12天海马CA1和CA3亚区解离的一小部分细胞(约1%)形成了神经球。绝大多数神经球细胞表达NSC标志物,如巢蛋白、Sox-2和Musashi-1。分化试验显示这些NSCs有能力分化为神经元、星形胶质细胞和少突胶质细胞。有趣的是,两个亚区NSCs的总体神经元分化随年龄下降(出生后第4天为23 - 28%,出生后第12天为5 - 10%),但NSCs向少突胶质细胞的分化程度随年龄增加(出生后第4天为24 - 32%,出生后第12天为45 - 55%)。然而,NSCs向星形胶质细胞的分化没有变化(40 - 48%)。此外,两个亚区的NSCs都能分化为γ-氨基丁酸(GABA)能神经元,包括表达钙结合蛋白、钙视网膜蛋白、神经肽Y和小白蛋白等标志物的亚类。然而,表达GABA的神经元比例在出生后第4天(59 - 67%)和出生后第12天(25 - 38%)之间下降。进一步分析显示,在出生后第4天和第12天动物的海马CA1和CA3亚区的不同层中存在增殖的NSC样细胞(即表达Ki-67和Sox-2的细胞)。因此,多能NSCs在出生后时期持续存在于海马的CA1和CA3亚区。这些NSCs也保留了产生GABA能和非GABA能神经元的能力。然而,它们在出生后早期的总体神经发生潜能显著下降。