Liang Anna C, Mandeville Emiri T, Maki Takakuni, Shindo Akihiro, Som Angel T, Egawa Naohiro, Itoh Kanako, Chuang Tsu Tshen, McNeish John D, Holder Julie C, Lok Josephine, Lo Eng H, Arai Ken
Neuroprotection Research Laboratory, Departments of Radiology and Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Cell Transplant. 2016;25(4):705-14. doi: 10.3727/096368916X690557. Epub 2016 Jan 22.
Aging and vascular comorbidities such as hypertension comprise critical cofactors that influence how the brain responds to stroke. Ischemic stress induces neurogenesis and oligodendrogenesis in younger brains. However, it remains unclear whether these compensatory mechanisms can be maintained even under pathologically hypertensive and aged states. To clarify the age-related remodeling capacity after stroke under hypertensive conditions, we assessed infarct volume, behavioral outcomes, and surrogate markers of neurogenesis and oligodendrogenesis in acute and subacute phases after transient focal cerebral ischemia in 3- and 12-month-old spontaneously hypertensive rats (SHRs). Hematoxylin and eosin staining showed that 3- and 12-month-old SHRs exhibited similar infarction volumes at both 3 and 14 days after focal cerebral ischemia. However, recovery of behavioral deficits (neurological score assessment and adhesive removal test) was significantly less in 12-month-old SHRs compared to 3-month-old SHRs. Concomitantly, numbers of nestin(+) neural stem/progenitor cells (NSPCs) near the infarct border area or subventricular zone in 12-month-old SHRs were lower than 3-month-old SHRs at day 3. Similarly, numbers of PDGFR-α(+) oligodendrocyte precursor cells (OPCs) in the corpus callosum were lower in 12-month-old SHRs at day 3. Lower levels of NSPC and OPC numbers were accompanied by lower expression levels of phosphorylated CREB. By day 14 postischemia, NSPC and OPC numbers in 12-month-old SHRs recovered to similar levels as in 3-month-old SHRs, but the numbers of proliferating NSPCs (Ki-67(+)nestin(+) cells) and proliferating OPCs (Ki-67(+)PDGFR-α(+) cells) remained lower in the older brains even at day 14. Taken together, these findings suggest that aging may also decrease poststroke compensatory responses for neurogenesis and oligodendrogenesis even under hypertensive conditions.
衰老和血管共病(如高血压)是影响大脑对中风反应方式的关键辅助因素。缺血应激在年轻大脑中诱导神经发生和少突胶质细胞生成。然而,目前尚不清楚即使在病理性高血压和衰老状态下,这些代偿机制是否能够维持。为了阐明高血压条件下中风后与年龄相关的重塑能力,我们评估了3个月和12个月大的自发性高血压大鼠(SHR)短暂性局灶性脑缺血后急性期和亚急性期的梗死体积、行为结果以及神经发生和少突胶质细胞生成的替代标志物。苏木精和伊红染色显示,3个月和12个月大的SHR在局灶性脑缺血后3天和14天的梗死体积相似。然而,与3个月大的SHR相比,12个月大的SHR行为缺陷(神经评分评估和黏附去除试验)的恢复明显较差。同时,在第3天,12个月大的SHR梗死边界区域或脑室下区附近的巢蛋白(+)神经干细胞/祖细胞(NSPC)数量低于3个月大的SHR。同样,在第3天,12个月大的SHR胼胝体中血小板衍生生长因子受体-α(+)少突胶质细胞前体细胞(OPC)数量较低。NSPC和OPC数量的降低伴随着磷酸化CREB表达水平的降低。到缺血后第14天,12个月大的SHR中的NSPC和OPC数量恢复到与3个月大的SHR相似的水平,但即使在第14天,老年大脑中增殖的NSPC(Ki-67(+)巢蛋白(+)细胞)和增殖的OPC(Ki-67(+)血小板衍生生长因子受体-α(+)细胞)数量仍然较低。综上所述,这些发现表明,即使在高血压条件下,衰老也可能降低中风后神经发生和少突胶质细胞生成的代偿反应。