Catts Vibeke Sørensen, Wong Jenny, Fillman Stu Gregory, Fung Samantha Jane, Shannon Weickert Cynthia
Schizophrenia Research Institute, Sydney, Australia Schizophrenia Research Laboratory, Neuroscience Research Australia, Sydney, Australia School of Psychiatry, University of New South Wales, Sydney, Australia
Illawarra Health and Medical Research Institute, University of Wollongong, Wollongong, Australia School of Biological Sciences, University of Wollongong, Wollongong, Australia.
Aust N Z J Psychiatry. 2014 Aug;48(8):722-34. doi: 10.1177/0004867414531078. Epub 2014 Apr 17.
While schizophrenia may have a progressive component, the evidence for neurodegenerative processes as indicated by reactive astrocytes is inconclusive. We recently identified a subgroup of individuals with schizophrenia with increased expression of inflammatory markers in prefrontal cortex, and hypothesized that this subgroup would also have reactive astrocytes.
We measured glial fibrillary acidic protein (GFAP) mRNA by quantitative real-time reverse transcriptase polymerase chain reaction (RT-PCR) and protein levels by immunoblotting in grey matter homogenate from 37 individuals with schizophrenia and 37 unaffected controls. We examined the morphology of GFAP-positive astrocytes in immunostained sections of middle frontal gyrus. We tested if GFAP expression or astrocyte morphology were altered in people with schizophrenia with increased expression of inflammatory markers. We used RNA-Seq data on a subset of patients and controls (n=20/group) to ascertain whether mRNA transcripts associated with astrogliosis were elevated in the individuals with active neuroinflammation.
GFAP (mRNA and protein) levels and astrocyte morphology were not significantly different between people with schizophrenia and controls overall. However, individuals with schizophrenia with neuroinflammation had increased expression of GFAP mRNA (t(33)=2.978, p=0.005), hypertrophic astrocyte morphology (χ(2)(2)=6.281, p=0.043), and statistically significant elevated expression of three mRNA transcripts previously associated with astrogliosis.
We found clear evidence of astrogliosis in a subset of people with schizophrenia. We suggest that the lack of astrogliosis reported in previous studies may be due to cohort differences in aetiopathology, illness stage, treatment exposure, or a failure to examine subsets of people with schizophrenia.
虽然精神分裂症可能有进行性成分,但反应性星形胶质细胞所表明的神经退行性过程的证据尚无定论。我们最近发现了一组前额叶皮质炎症标志物表达增加的精神分裂症患者,并假设该亚组也会有反应性星形胶质细胞。
我们通过定量实时逆转录聚合酶链反应(RT-PCR)测量了37例精神分裂症患者和37例未受影响对照者灰质匀浆中的胶质纤维酸性蛋白(GFAP)mRNA,并通过免疫印迹法测量了其蛋白水平。我们检查了额中回免疫染色切片中GFAP阳性星形胶质细胞的形态。我们测试了炎症标志物表达增加的精神分裂症患者中GFAP表达或星形胶质细胞形态是否改变。我们使用了一部分患者和对照(每组n = 20)的RNA测序数据,以确定与星形胶质细胞增生相关的mRNA转录本在有活动性神经炎症的个体中是否升高。
总体而言,精神分裂症患者和对照者之间的GFAP(mRNA和蛋白)水平及星形胶质细胞形态没有显著差异。然而,有神经炎症的精神分裂症患者GFAP mRNA表达增加(t(33)=2.978,p = 0.005),星形胶质细胞形态肥大(χ(2)(2)=6.281,p = 0.043),并且之前与星形胶质细胞增生相关的三种mRNA转录本的表达在统计学上显著升高。
我们在一部分精神分裂症患者中发现了星形胶质细胞增生的明确证据。我们认为,先前研究中报道的缺乏星形胶质细胞增生可能是由于病因病理学、疾病阶段、治疗暴露方面的队列差异,或者是未能检查精神分裂症患者的亚组。