Table 3. Human brain tissue used in Fig. 5

Sample (lanes)

Diagnosis

Brain region

Age

PMD, h

LB load

1

Control

Cingulate cortex

66

10

0

2

Control

Cingulate cortex

74

4

0

3

AD

Cingulate cortex

88

14

0

4

AD

Cingulate cortex

80

9

0

5

PD/MID/cortical LBs

Midfrontal gyrus

75

9

1

6

PD/LBD

Midfrontal gyrus

90

16

3

7

PD/AD

Midfrontal gyrus

64

21

2

8

PD/AD prob./LB changes

Cingulate cortex

82

5

10

9

PD/MID/cortical LBs

Cingulate cortex

75

9

12

10

PD/diffuse Ab deposits

Cingulate cortex

77

16

18.5

11

PD/AD/LB

Cingulate cortex

84

12

20

12

PD/AD

Cingulate cortex

64

21

20

13

AD/PD

Frontal cortex

81

33

20

14

AD

Cingulate cortex

78

4

20+

AD, Alzheimer’s disease; LB, Lewy body; LBD, LB dementia, MID, mutiple infarct

dementia; PD, Parkinson’s disease; PMD, postmortem delay. Brain tissues were obtained from the Brain Resource Center (Department of Pathology, Johns Hopkins University School of Medicine). At autopsy, one hemibrain was cut and stored at –80° C, and another hemi-brain was fixed in formalin, and tissue blocks were embedded in paraffin for histological analysis. The pathological diagnosis of AD was formulated according to the Consortium to Establish a Registry for Alzheimer's Disease (1), and PD was formulated according to the criteria proposed by McKeith et al. (2). LB/LN loads were determined by semi-quantitative analysis of a -Syn-immunostained paraffin sections. Briefly, 10-m m paraffin sections were pretreated with formic acid and immunostained with Syn-1 antibody. The LB load was determined by counting the number of LBs per ´ 100 microscopic field, corresponding to 3.14 mm2, by using a light microscope interfaced with a Microbrightfield Sterology System (3). The samples in bold were used for the semiquantitative analysis.

1. Mirra, S. S., Heyman, A., McKeel, D., Sumi, S. M., Crain, B. J., Brownlee, L. M., Vogel, F. S., Hughes, J. P., van Belle, G. & Berg, L. (1991) Neurology 41, 479–486.

2. McKeith, I. G., Galasko, D., Kosaka, K., Perry, E. K., Dickson, D. W., Hansen, L. A., Salmon, D. P., Lowe, J., Mirra, S. S., Byrne, E. J. et al. (1996) Neurology 47, 1113–1124.

3. Pletnikova, O., West, N., Lee, M. K., Rudow, G., Dawson, T. M., Marsh, L. & Troncoso, J. C. (December 28, 2004) Neurobiol. Aging, 10.1016/j.neurobiolaging.2004.10.006.