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To quantify mitochondrial accumulation at the junctions, we applied multiple immunolabeling, correlated confocal laser scanning , and a semi-automated unbiased technique (Figures 2L-2S).

We found that, at each investigated age, TOM20 immunofluorescence depth within the cell our bodies and proximal tufts of DCX+ neurons was substantially larger at websites of microglial contact compared with adjacent areas . These outcomes confirmed that neuronal mitochondria are strongly enriched at...
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To quantify mitochondrial accumulation at the junctions, we applied multiple immunolabeling, correlated confocal laser scanning , and a semi-automated unbiased technique (Figures 2L-2S).

We found that, at each investigated age, TOM20 immunofluorescence depth within the cell our bodies and proximal tufts of DCX+ neurons was substantially larger at websites of microglial contact compared with adjacent areas . These outcomes confirmed that neuronal mitochondria are strongly enriched at...
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To quantify mitochondrial accumulation at the junctions, we applied multiple immunolabeling, correlated confocal laser scanning , and a semi-automated unbiased technique (Figures 2L-2S).

We found that, at each investigated age, TOM20 immunofluorescence depth within the cell our bodies and proximal tufts of DCX+ neurons was substantially larger at websites of microglial contact compared with adjacent areas . These outcomes confirmed that neuronal mitochondria are strongly enriched at...
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To quantify mitochondrial accumulation at the junctions, we applied multiple immunolabeling, correlated confocal laser scanning , and a semi-automated unbiased technique (Figures 2L-2S).

We found that, at each investigated age, TOM20 immunofluorescence depth within the cell our bodies and proximal tufts of DCX+ neurons was substantially larger at websites of microglial contact compared with adjacent areas . These outcomes confirmed that neuronal mitochondria are strongly enriched at...
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