Table 2.
Basement Membrane Coverage of Endothelial Sprouts on Tumor Blood Vessels*
| RIP-Tag2 pancreatic islet tumors | MCa-IV mammary carcinomas | Lewis lung carcinomas | |
|---|---|---|---|
| Length of CD31-immunoreactive endothelial sprouts (range) | 13 ± 1 μm (5–35 μm) | 32 ± 5 μm (11–61 μm) | 20 ± 4 μm (5–49 μm) |
| Length of type IV collagen-immunoreactive sleeve on endothelial sprouts (range) | 23 ± 2 μm (7–41 μm) | 54 ± 9 μm (14–90 μm) | 30 ± 5 μm (9–75 μm) |
| Length of portion of type IV collagen-immunoreactive sleeve beyond tip of CD31-staining | 10 ± 3 μm | 22 ± 3 μm | 10 ± 3 μm |
| Length of type IV collagen-immunoreactive sleeve on endothelial sprouts expressed as % of length of CD31-stained sprout | 175 ± 18% | 170 ± 7% | 153 ± 18% |
| Length of pericyte processes on sprouts expressed as % of length of CD31-stained sprout† | 180% | 162% | 138% |
| Percent of sprouts with naked tips (length of naked tips of sprouts) | 5% (4.8 μm) | 5% (5.5 μm) | 5% (4.2 μm) |
*Endothelial sprouts, identified as thin, tapered, blind-ended CD31-immunoreactive projections away from the vascular axis, were analyzed in 80-μm sections of tumors double-stained for type IV collagen and CD31 immunoreactivities. Naked tips represent the distal-most region of CD31 staining of sprouts with no detectable type IV collagen immunoreactivity. No sprouts were identified on blood vessels of normal pancreatic islets. Values are expressed as means ± SE (n = 4 mice per group). Ten sprouts were examined in each mouse. Ranges are values for 40 sprouts per group.
†Pericyte data from Morikawa et al. (2002). 10