Kühne Britta Anna, Gutierrez-Vázquez Lara, Sánchez Lamelas Estela, Guardia-Escote Laia, Pla Laura, Loreiro Carla, Gratacós Eduard, Barenys Marta, Illa Miriam
Grup de Recerca en Toxicologia (GRET) i INSA-UB, Departament de Farmacologia, Toxicologia i Química Terapèutica, Facultat de Farmàcia i Ciències de l'Alimentació, Universitat de Barcelona, Barcelona, Spain.
BCNatal | Fetal Medicine Research Center (Hospital Clínic and Hospital Sant Joan de Déu), Universitat de Barcelona, Barcelona, Spain.
Front Cell Neurosci. 2023 Apr 26;17:1116405. doi: 10.3389/fncel.2023.1116405. eCollection 2023.
Intrauterine growth restriction (IUGR) is a well-known cause of impaired neurodevelopment during life. In this study, we aimed to characterize alterations in neuronal development underlying IUGR and discover strategies to ameliorate adverse neurodevelopment effects by using a recently established rabbit in vitro neurosphere culture.
IUGR was surgically induced in pregnant rabbits by ligation of placental vessels in one uterine horn, while the contralateral horn remained unaffected for normal growth (control). At this time point, rabbits were randomly assigned to receive either no treatment, docosahexaenoic acid (DHA), melatonin (MEL), or lactoferrin (LF) until c-section. Neurospheres consisting of neural progenitor cells were obtained from control and IUGR pup's whole brain and comparatively analyzed for the ability to differentiate into neurons, extend neurite length, and form dendritic branching or pre-synapses. We established for the very first time a protocol to cultivate control and IUGR rabbit neurospheres not only for 5 days but under long-term conditions up to 14 days under differentiation conditions. Additionally, an in vitro evaluation of these therapies was evaluated by exposing neurospheres from non-treated rabbits to DHA, MEL, and SA (sialic acid, which is the major lactoferrin compound) and by assessing the ability to differentiate neurons, extend neurite length, and form dendritic branching or pre-synapses.
We revealed that IUGR significantly increased the neurite length after 5 days of cultivation in vitro, a result in good agreement with previous in vivo findings in IUGR rabbits presenting more complex dendritic arborization of neurons in the frontal cortex. MEL, DHA, and SA decreased the IUGR-induced length of primary dendrites , however, only SA was able to reduce the total neurite length to control level in IUGR neurospheres. After prenatal administration of SAs parent compound LF with subsequent evaluation , LF was able to prevent abnormal neurite extension.
We established for the first time the maintenance of the rabbit neurosphere culture for 14 days under differentiation conditions with increasing complexity of neuronal length and branching up to pre-synaptic formation. From the therapies tested, LF or its major compound, SA, prevents abnormal neurite extension and was therefore identified as the most promising therapy against IUGR-induced changes in neuronal development.
宫内生长受限(IUGR)是生活中神经发育受损的一个众所周知的原因。在本研究中,我们旨在通过使用最近建立的兔体外神经球培养来表征IUGR潜在的神经元发育改变,并发现改善不良神经发育影响的策略。
通过结扎一个子宫角的胎盘血管,在怀孕兔中手术诱导IUGR,而对侧子宫角保持不受影响以实现正常生长(对照)。在这个时间点,将兔随机分配为不接受治疗、接受二十二碳六烯酸(DHA)、褪黑素(MEL)或乳铁蛋白(LF),直至剖宫产。从对照和IUGR幼崽的全脑中获得由神经祖细胞组成的神经球,并对其分化为神经元的能力、神经突长度的延伸以及形成树突分支或突触前结构的能力进行比较分析。我们首次建立了一个方案,不仅在分化条件下将对照和IUGR兔神经球培养5天,而且在长期条件下培养长达14天。此外,通过将未治疗兔的神经球暴露于DHA、MEL和SA(唾液酸,乳铁蛋白的主要化合物),并评估其分化为神经元的能力、神经突长度的延伸以及形成树突分支或突触前结构能力,对这些疗法进行体外评估。
我们发现,在体外培养5天后,IUGR显著增加了神经突长度,这一结果与先前在IUGR兔体内的研究结果一致,即IUGR兔额叶皮质神经元的树突分支更复杂。MEL、DHA和SA减少了IUGR诱导的初级树突长度,然而,只有SA能够将IUGR神经球中的总神经突长度降低到对照水平。在产前给予SA的母体化合物LF并进行后续评估后,LF能够预防异常神经突延伸。
我们首次在分化条件下将兔神经球培养维持了14天,神经元长度和分支的复杂性不断增加,直至形成突触前结构。在所测试的疗法中,LF或其主要化合物SA可预防异常神经突延伸,因此被确定为对抗IUGR诱导的神经元发育变化最有前景的疗法。