Center for Metabolic Disease Research, Temple University Lewis Katz School of Medicine, 3500 N Broad Street, Philadelphia, PA 19140, United States; Department of Pathology and Laboratory Medicine, Temple University Lewis Katz School of Medicine, 3500 N Broad Street, Philadelphia, PA 19140, United States.
Department of Clinical Science, Temple University Lewis Katz School of Medicine, 3500 N Broad Street, Philadelphia, PA 19140, United States.
Brain Behav Immun. 2019 Aug;80:488-499. doi: 10.1016/j.bbi.2019.04.029. Epub 2019 Apr 16.
Varying degrees of cognitive deficits affect over half of all HIV-1 infected patients. Because of antiretroviral treatment (ART) regimens, the HIV-1 patient population is increasing in age. Very few epidemiological studies have focused on sex-specific differences in HIV-1-associated neurocognitive disorders (HAND). The purpose of this study is to examine any possible differences between male and female mice in the progression of cognitive dementia during persistent low-level HIV-1 protein exposure, mimicking the typical clinical setting in the post-ART era. Eight to ten-month old HIV-1 Tg26(+/-) transgenic mice were utilized to assess for specific learning and memory modalities. Initial physiological screening and fear conditioning assessments revealed that Tg26 mice exhibited no significant differences in general behavioral function, contextual fear conditioning, or cued fear conditioning responses when compared to their wild-type (WT) littermates, regardless of sex. However, Barnes maze testing revealed significantly impaired short and long-term spatial memory in males, while females had impaired spatial learning abilities and short-term spatial memory. The potential cellular mechanism underlying these sex-specific neurocognitive deficits was explored with hippocampal neurogenic analysis. Compared to WT mice, both male and female Tg26(+/-) mice had fewer quiescent neural stem cells and neuroblasts in their hippocampi. Male Tg26(+/-) mice had a more robust reduction of the quiescent neural stem cell pool than female Tg26(+/-) mice. While female WT mice had a higher number of neural progenitor cells than male WT mice, only female Tg26(+/-) mice exhibited a robust reduction in the number of neural progenitor cells. Altogether, these results suggest that middle-aged male and female Tg26(+/-) mice manifest differing impairments in cognitive functioning and hippocampal neurogenesis. This study emphasizes the importance of understanding sex related differences in HAND pathology, which would aid in designing more optimized therapeutic regimens for the treatment of HAND.
不同程度的认知缺陷影响了超过一半的 HIV-1 感染患者。由于抗逆转录病毒治疗 (ART) 方案的实施,HIV-1 患者人群的年龄正在增长。很少有流行病学研究关注 HIV-1 相关神经认知障碍 (HAND) 的性别特异性差异。本研究旨在研究在持续低水平 HIV-1 蛋白暴露下,模拟抗逆转录病毒治疗后时代的典型临床环境,雄性和雌性小鼠在认知痴呆进展方面是否存在差异。研究使用了 8 至 10 个月大的 HIV-1 Tg26(+/-)转基因小鼠来评估特定的学习和记忆方式。初步的生理筛选和恐惧条件反射评估表明,与野生型 (WT) 同窝仔鼠相比,Tg26 小鼠在一般行为功能、情境恐惧条件反射或线索恐惧条件反射反应方面没有显著差异,无论性别如何。然而,Barnes 迷宫测试显示,雄性小鼠的短期和长期空间记忆明显受损,而雌性小鼠的空间学习能力和短期空间记忆受损。使用海马神经发生分析探索了这些性别特异性神经认知缺陷的潜在细胞机制。与 WT 小鼠相比,雄性和雌性 Tg26(+/-)小鼠的海马神经干细胞和神经前体细胞数量均减少。雄性 Tg26(+/-)小鼠的静息神经干细胞池减少幅度比雌性 Tg26(+/-)小鼠更为显著。虽然雌性 WT 小鼠的神经祖细胞数量多于雄性 WT 小鼠,但只有雌性 Tg26(+/-)小鼠的神经祖细胞数量明显减少。总之,这些结果表明,中年雄性和雌性 Tg26(+/-)小鼠在认知功能和海马神经发生方面表现出不同的损伤。本研究强调了理解 HAND 病理性别差异的重要性,这将有助于设计更优化的 HAND 治疗方案。