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Table 4 Localization and change of lipopolysaccharides in Alzheimer’s disease

From: Gram-negative bacteria and their lipopolysaccharides in Alzheimer’s disease: pathologic roles and therapeutic implications

Source

Subject

Method

Main findings

References

Brain

AD patients

Immunoblot

LPS was detected in the area adjacent to the lateral ventricle of the parietal lobe of AD brain

[38]

AD patients

WB

IHC

LPS was detected in temporal lobe neocortex perinuclear region of AD brain

LPS was co-localized with Aβ plaque

[125]

AD patients

IF

WB

LPS was detected in superior temporal gyrus gray matter, frontal lobe white matter, and periventricular white matter of AD brain

LPS was localized with Aβ plaque, neurons, microglia, and oligodendrocytes

[15]

AD patients

IHC

LPS was detected in superior temporal lobe neocortex of AD brain

LPS was localized in neurons

[124]

AD patients

WB

LPS was detected in temporal lobe neocortex and hippocampus of AD brain

[123]

5×FAD mice

IF

LPS was detected in pyramidal and stratum oriens regions of hippocampus of AD brain

LPS was co-localized with LPS-phagocytic cell

[23]

Blood

AD patients

LAL assay

LPS levels in AD patients were 3- to 6-fold compared with that in control

[22]

5×FAD mice

ELISA

LPS levels in AD mice were 4-fold compared with that in control

[23]

5×FAD mice

LAL assay

LPS levels in AD mice were 4-fold compared with that in control

[136]

Feces

5×FAD mice

LAL assay

LPS levels in AD mice were 3- to 4-fold compared with that in control

[23, 136]

  1. AD Alzheimer’s disease, ELISA Enzyme-linked immunosorbent assay, IF immunofluorescence, IHC immunohistochemistry, LAL assay limulus amebocyte lysate assay, LPS lipopolysaccharides, WB western blot