TABLE 2.
Expression of various T-cell surface molecules on two T-cell lines after incubation with various reagentsa
Reagent | Mean fluorescence intensity
|
|||||||||
---|---|---|---|---|---|---|---|---|---|---|
Anti-CD28
|
Anti-CD45RA
|
Anti-CD2
|
Anti-CD18
|
Anti-L-selectin
|
||||||
Ju | JR | Ju | JR | Ju | JR | Ju | JR | Ju | JR | |
Medium | 15 | 0 | 28 | 19 | 43 | 43 | 21 | 20 | 100 | 93 |
PMA | 13 | 0 | 29 | 21 | 51 | 51 | 24 | 19 | 17 | 13 |
GXM | 16 | 0 | 28 | 21 | 47 | 51 | 21 | 20 | 41 | 70 |
GalXM | 16 | 0 | 28 | 21 | 44 | 45 | 21 | 22 | 87 | 87 |
MP | 15 | 0 | 28 | 21 | 44 | 44 | 21 | 20 | 97 | 87 |
Ju, Jurkat; JR, J.RT3-T3.5. The T cells (106) were incubated for 2 h at 37°C with 100 ng of PMA/ml or 1 mg of GXM, GalXM, or MP/ml in serum-free RPMI 1640 medium. CD28, CD45RA, CD2, CD18, or L-selectin expression on the two T-cell lines was determined by immunofluorescence staining with the designated antibody and subjecting the cells to flow cytometric analysis. The data are from one experiment representative of the two experiments performed.