中文摘要：

小膠質(zhì)細(xì)胞是大腦駐留的巨噬細(xì)胞，可以獲得不同的功能表型分享，這些表型得到了細(xì)胞代謝差異重編程的支持講實踐。這些適應(yīng)包括糖酵解和線粒體代謝通量的重塑保供，可能會(huì)改變組織水平的能量底物可用性大型。這種現(xiàn)象可能與大腦高度相關(guān)，因?yàn)樵诖竽X中不難發現，新陳代謝必須得到精確調(diào)節(jié)研究進展，以維持適當(dāng)?shù)纳窠?jīng)元興奮性和突觸傳遞。然而智慧與合力，小膠質(zhì)細(xì)胞可以影響神經(jīng)元能量代謝的直接證據(jù)一直缺乏喜愛。結(jié)合分子分析、電生理學(xué)開放要求、氧微傳感器記錄和數(shù)學(xué)建模向好態勢，我們研究了神經(jīng)炎癥期間小膠質(zhì)細(xì)胞介導(dǎo)的大腦能量紊亂。我們的結(jié)果表明服務機製，促炎小膠質(zhì)細(xì)胞表現(xiàn)出增強(qiáng)的一氧化氮釋放和 CX3CR1 表達(dá)降低貢獻力量，短暫增加了組織乳酸/葡萄糖比率，這取決于小膠質(zhì)細(xì)胞中的轉(zhuǎn)錄重編程更多可能性，而不是神經(jīng)元中的轉(zhuǎn)錄重編程去創新。在這種情況下，神經(jīng)網(wǎng)絡(luò)活動(dòng)緊迫性，如伽馬振蕩（30-70 Hz）可以通過線粒體中ATP的產(chǎn)生增加來推動(dòng)結構，這反映在耗氧量增加上。在失調(diào)的炎癥期間高效，高能量需求和低葡萄糖可用性可能是神經(jīng)元代謝適應(yīng)性的邊界條件溝通協調，正如單神經(jīng)元能量學(xué)的動(dòng)力學(xué)模型所揭示的那樣要素配置改革。總的來說帶動擴大，這些發(fā)現(xiàn)表明核心技術體系，在中度神經(jīng)炎癥期間，代謝靈活性可以保護(hù)神經(jīng)元網(wǎng)絡(luò)功能免受局部底物可用性的改變持續發展。必然趨勢。

英文摘要：

Microglia, brain-resident macrophages, can acquire distinct functional phenotypes, which are supported by differential reprogramming of cell metabolism. These adaptations include remodeling in glycolytic and mitochondrial metabolic fluxes, potentially altering energy substrate availability at the tissue level. This phenomenon may be highly relevant in the brain, where metabolism must be precisely regulated to maintain appropriate neuronal excitability and synaptic transmission. Direct evidence that microglia can impact on neuronal energy metabolism has been widely lacking, however. Combining molecular profiling, electrophysiology, oxygen microsensor recordings and mathematical modeling, we investigated microglia-mediated disturbances in brain energetics during neuroinflammation. Our results suggest that proinflammatory microglia showing enhanced nitric oxide release and decreased CX3CR1 expression transiently increase the tissue lactate/glucose ratio that depends on transcriptional reprogramming in microglia, not in neurons. In this condition, neuronal network activity such as gamma oscillations (30–70 Hz) can be fueled by increased ATP production in mitochondria, which is reflected by elevated oxygen consumption. During dysregulated inflammation, high energy demand and low glucose availability can be boundary conditions for neuronal metabolic fitness as revealed by kinetic modeling of single neuron energetics. Collectively, these findings indicate that metabolic flexibility protects neuronal network function against alterations in local substrate availability during moderate neuroinflammation.

論文信息：

論文題目：Metabolic flexibility ensures proper neuronal network function in moderate neuroinflammation

期刊名稱：Scientific Reports

時(shí)間期卷：volume 14, Article number: 14405 (2024) pages685–700 (2024)

在線時(shí)間：2024年6月22日

研究亮點(diǎn)：

代謝靈活性確保了炎癥期間神經(jīng)元網(wǎng)絡(luò)的正常功能。在體內(nèi)平衡中擴大，血液輸入葡萄糖的消耗和腦細(xì)胞平行產(chǎn)生乳酸多樣性，從乳酸/葡萄糖比值低的血管周圍空間到實(shí)質(zhì)（該比率增加）產(chǎn)生溫和的能量底物梯度。在炎癥期間新格局，小膠質(zhì)細(xì)胞葡萄糖消耗和乳酸產(chǎn)生通過代謝重編程得到增強(qiáng)明顯，這導(dǎo)致更高的乳酸/葡萄糖比率，加劇了血管周圍空間和腦實(shí)質(zhì)之間的能量底物梯度顯示。在這種情況下創新為先，神經(jīng)元網(wǎng)絡(luò)活動(dòng)可能會(huì)通過平行增加耗氧量來保持。炎癥期間神經(jīng)元能量適應(yīng)性的邊界是高能量需求伴隨著極低的葡萄糖可用性科普活動。在炎癥失調(diào)的生態(tài)位中可能會(huì)達(dá)到這些限制創新延展，其中反應(yīng)性小膠質(zhì)細(xì)胞的聚集可能發(fā)生在遠(yuǎn)離毛細(xì)血管的區(qū)域。

材料方法：

氯膦酸鹽脂質(zhì)體巨噬細(xì)胞清除劑Clodronateliposomes（liposoma長期間，CP-005-005）加入培養(yǎng)基清除小膠質(zhì)巨噬細(xì)胞基本情況，可以參考這篇文獻(xiàn)。腦切片體外培養(yǎng)高端化，文獻(xiàn)濃度是100ug/ml力量。荷蘭liposoma巨噬細(xì)胞清除劑Clodronate Liposomes的濃度是5mg/ml。僅僅體外實(shí)驗(yàn)才建議稀釋不負眾望，用無菌PBS稀釋高效流通。