Centre of Perinatal Medicine and Health, Institute of Neuroscience and Physiology, Department of Physiology, Sahlgrenska Academy, University of Gothenburg, 40530, Gothenburg, Sweden.
Centre for the Developing Brain, Department of Perinatal Imaging and Health, School of Biomedical Engineering and Imaging Sciences, King's College London, King's Health Partners, St Thomas' Hospital, London, UK.
Acta Neuropathol Commun. 2021 Oct 15;9(1):166. doi: 10.1186/s40478-021-01267-7.
Osteopontin (OPN) is a matricellular protein that mediates various physiological functions and is implicated in neuroinflammation, myelination, and perinatal brain injury. However, its expression in association with brain injury in preterm infants is unexplored. Here we examined the expression of OPN in postmortem brains of preterm infants and explored how this expression is affected in brain injury. We analyzed brain sections from cases with white matter injury (WMI) and cases with germinal matrix hemorrhage (GMH) and compared them to control cases having no brain injury. WMI cases displayed moderate to severe tissue injury in the periventricular and deep white matter that was accompanied by an increase of microglia with amoeboid morphology. Apart from visible hemorrhage in the germinal matrix, GMH cases displayed diffuse white matter injury in the periventricular and deep white matter. In non-injured preterm brains, OPN was expressed at low levels in microglia, astrocytes, and oligodendrocytes. OPN expression was significantly increased in regions with white matter injury in both WMI cases and GMH cases. The main cellular source of OPN in white matter injury areas was amoeboid microglia, although a significant increase was also observed in astrocytes in WMI cases. OPN was not expressed in the germinal matrix of any case, regardless of whether there was hemorrhage. In conclusion, preterm brain injury induces elevated OPN expression in microglia and astrocytes, and this increase is found in sites closely related to injury in the white matter regions but not with the hemorrhage site in the germinal matrix. Thus, it appears that OPN takes part in the inflammatory process in white matter injury in preterm infants, and these findings facilitate our understanding of OPN's role under both physiological and pathological conditions in the human brain that may lead to greater elucidation of disease mechanisms and potentially better treatment strategies.
骨桥蛋白(OPN)是一种基质细胞蛋白,它介导各种生理功能,并与神经炎症、髓鞘形成和围产期脑损伤有关。然而,它在早产儿脑损伤中的表达尚未被研究。在这里,我们检查了早产儿尸检脑样本中 OPN 的表达,并探讨了其在脑损伤中的表达如何受到影响。我们分析了伴有白质损伤(WMI)和伴有脑室内出血(GMH)病例的脑切片,并与无脑损伤的对照组进行比较。WMI 病例显示在脑室周围和深部白质中存在中度至重度组织损伤,伴有阿米巴样形态的小胶质细胞增多。除了在脑室内可见出血外,GMH 病例还显示在脑室周围和深部白质中有弥漫性白质损伤。在未受伤的早产儿脑中,OPN 在小胶质细胞、星形胶质细胞和少突胶质细胞中表达水平较低。在 WMI 病例和 GMH 病例中,白质损伤区域的 OPN 表达均显著增加。在白质损伤区域中,OPN 的主要细胞来源是阿米巴样小胶质细胞,尽管在 WMI 病例中星形胶质细胞的表达也显著增加。在任何病例的脑室内基质中均未检测到 OPN 的表达,无论是否存在出血。总之,早产儿脑损伤诱导小胶质细胞和星形胶质细胞中 OPN 表达升高,这种增加发生在与白质损伤部位密切相关的部位,但不在脑室内出血部位。因此,似乎 OPN 参与了早产儿白质损伤中的炎症过程,这些发现有助于我们理解 OPN 在人类大脑的生理和病理条件下的作用,可能会更好地阐明疾病机制,并制定出更好的治疗策略。