The Roskamp Institute, 2040 Whitfield Avenue, Sarasota, FL, 34243, USA.
The Open University, Walton Hall, Kents Hill, Milton Keynes, MK7 6AA, UK.
J Neuroinflammation. 2024 Aug 3;21(1):194. doi: 10.1186/s12974-024-03173-w.
Chronic neuroinflammation and microglial activation are key mediators of the secondary injury cascades and cognitive impairment that follow exposure to repetitive mild traumatic brain injury (r-mTBI). Peroxisome proliferator-activated receptor-γ (PPARγ) is expressed on microglia and brain resident myeloid cell types and their signaling plays a major anti-inflammatory role in modulating microglial responses. At chronic timepoints following injury, constitutive PPARγ signaling is thought to be dysregulated, thus releasing the inhibitory brakes on chronically activated microglia. Increasing evidence suggests that thiazolidinediones (TZDs), a class of compounds approved from the treatment of diabetes mellitus, effectively reduce neuroinflammation and chronic microglial activation by activating the peroxisome proliferator-activated receptor-γ (PPARγ). The present study used a closed-head r-mTBI model to investigate the influence of the TZD Pioglitazone on cognitive function and neuroinflammation in the aftermath of r-mTBI exposure. We revealed that Pioglitazone treatment attenuated spatial learning and memory impairments at 6 months post-injury and reduced the expression of reactive microglia and astrocyte markers in the cortex, hippocampus, and corpus callosum. We then examined whether Pioglitazone treatment altered inflammatory signaling mechanisms in isolated microglia and confirmed downregulation of proinflammatory transcription factors and cytokine levels. To further investigate microglial-specific mechanisms underlying PPARγ-mediated neuroprotection, we generated a novel tamoxifen-inducible microglial-specific PPARγ overexpression mouse line and examined its influence on microglial phenotype following injury. Using RNA sequencing, we revealed that PPARγ overexpression ameliorates microglial activation, promotes the activation of pathways associated with wound healing and tissue repair (such as: IL10, IL4 and NGF pathways), and inhibits the adoption of a disease-associated microglia-like (DAM-like) phenotype. This study provides insight into the role of PPARγ as a critical regulator of the neuroinflammatory cascade that follows r-mTBI in mice and demonstrates that the use of PPARγ agonists such as Pioglitazone and newer generation TZDs hold strong therapeutic potential to prevent the chronic neurodegenerative sequelae of r-mTBI.
慢性神经炎症和小胶质细胞激活是反复轻度创伤性脑损伤(r-mTBI)后继发性损伤级联和认知障碍的关键介质。过氧化物酶体增殖物激活受体-γ(PPARγ)在小胶质细胞和脑驻留髓样细胞类型上表达,其信号转导在调节小胶质细胞反应中发挥主要的抗炎作用。在损伤后的慢性时间点,组成型 PPARγ 信号被认为失调,从而释放对慢性激活的小胶质细胞的抑制性刹车。越来越多的证据表明,噻唑烷二酮类(TZDs),一类用于治疗糖尿病的化合物,通过激活过氧化物酶体增殖物激活受体-γ(PPARγ),有效减轻神经炎症和慢性小胶质细胞激活。本研究使用闭合性头部 r-mTBI 模型,研究 TZD 吡格列酮对 r-mTBI 暴露后认知功能和神经炎症的影响。我们发现,吡格列酮治疗可减轻损伤后 6 个月的空间学习和记忆障碍,并降低皮质、海马体和胼胝体中反应性小胶质细胞和星形胶质细胞标志物的表达。然后,我们检查了吡格列酮治疗是否改变了分离的小胶质细胞中的炎症信号机制,并证实了促炎转录因子和细胞因子水平的下调。为了进一步研究 PPARγ 介导的神经保护作用中小胶质细胞特异性机制,我们生成了一种新型他莫昔芬诱导的小胶质细胞特异性 PPARγ 过表达小鼠系,并检查了其对损伤后小胶质细胞表型的影响。通过 RNA 测序,我们发现 PPARγ 过表达可改善小胶质细胞激活,促进与伤口愈合和组织修复相关的途径的激活(如:IL10、IL4 和 NGF 途径),并抑制采用疾病相关的小胶质细胞样(DAM-like)表型。这项研究提供了关于 PPARγ 作为 r-mTBI 后小鼠神经炎症级联反应的关键调节剂的作用的见解,并表明使用 PPARγ 激动剂(如吡格列酮和新一代 TZDs)具有很强的治疗潜力,可以预防 r-mTBI 的慢性神经退行性后遗症。