Sveinsdóttir Kristbjörg, Länsberg John-Kalle, Sveinsdóttir Snjólaug, Garwicz Martin, Ohlsson Lennart, Hellström Ann, Smith Lois, Gram Magnus, Ley David
Department of Pediatrics, Lund University, Lund, Sweden.
Dev Neurosci. 2017;39(6):487-497. doi: 10.1159/000480428. Epub 2017 Oct 4.
Cerebellar growth is impeded following very preterm birth in human infants and the observed reduction in cerebellar volume is associated with neurodevelopmental impairment. Decreased levels of circulating insulin-like growth factor 1 (IGF-1) are associated with decreased cerebellar volume. The relationship between preterm birth, circulating IGF-1, and key cell populations supporting cerebellar proliferation is unknown. The aim of this study was to evaluate the effect of preterm birth on postnatal growth, circulating IGF-1, and cerebellar maturation in a preterm rabbit pup model. Preterm rabbit pups (PT) were delivered by cesarean section at day 29 of gestation, cared for in closed incubators with humidified air, and gavage fed with formula. Control term pups (T) delivered by spontaneous vaginal delivery at day 32 of gestation were housed and fed by their lactating doe. In vivo perfusion-fixation for immunohistochemical evaluation of cerebellar proliferation, cell maturation, and apoptosis was performed at repeated time points in PT and T pups. Results show that the mean weight of the pups and circulating IGF-1 protein levels were lower in the PT group at all time points (p < 0.05) than in the T group. Postnatal weight development correlated with circulating IGF-1 (r2 = 0.89) independently of gestational age at birth and postnatal age. The proliferative (Ki-67-positive) portion of the external granular layer (EGL) was decreased in the PT group at postnatal day 2 (P2) compared to in the T group (p = 0.01). Purkinje cells exhibited decreased calbindin staining at P0 (p = 0.003), P2 (p = 0.004), and P5 (p = 0.04) in the PT group compared to in the T group. Staining for sonic hedgehog was positive in neuronal EGL progenitors and Purkinje cells at early time points but was restricted to a well-defined Purkinje cell monolayer at later time points. Preterm birth in rabbit pups is associated with lower circulating levels of IGF-1, decreased postnatal growth, and decreased cerebellar EGL proliferation and Purkinje cell maturation. The preterm rabbit pup model exhibits important characteristics of human preterm birth, and may thus be suitable for the evaluation of interventions aiming to modify growth and cerebellar development in the preterm population.
人类婴儿极早产会阻碍小脑生长,观察到的小脑体积减小与神经发育障碍有关。循环胰岛素样生长因子1(IGF-1)水平降低与小脑体积减小有关。早产、循环IGF-1与支持小脑增殖的关键细胞群之间的关系尚不清楚。本研究的目的是在早产兔幼崽模型中评估早产对出生后生长、循环IGF-1和小脑成熟的影响。早产兔幼崽(PT)在妊娠第29天通过剖宫产分娩,在装有湿润空气的封闭孵化器中饲养,并用配方奶灌胃喂养。妊娠第32天通过自然阴道分娩的足月对照幼崽(T)由其哺乳母兔饲养和喂养。在PT和T组幼崽的重复时间点进行体内灌注固定,用于小脑增殖、细胞成熟和凋亡的免疫组织化学评估。结果显示,在所有时间点,PT组幼崽的平均体重和循环IGF-1蛋白水平均低于T组(p < 0.05)。出生后体重发育与循环IGF-1相关(r2 = 0.89),与出生时的胎龄和出生后年龄无关。与T组相比,PT组在出生后第2天(P2)的外颗粒层(EGL)增殖部分(Ki-67阳性)减少(p = 0.01)。与T组相比,PT组在P0(p = 0.003)、P2(p = 0.004)和P5(p = 0.04)时浦肯野细胞的钙结合蛋白染色减少。在早期时间点,音猬因子在神经元EGL祖细胞和浦肯野细胞中染色呈阳性,但在后期时间点仅限于明确的浦肯野细胞单层。兔幼崽早产与循环IGF-1水平降低、出生后生长减少以及小脑EGL增殖和浦肯野细胞成熟减少有关。早产兔幼崽模型表现出人类早产的重要特征,因此可能适用于评估旨在改善早产人群生长和小脑发育的干预措施。