Figure 2.
General features of TCRA repertoire reconstitution. (A) Sharing of identifiable TCR clones between the donor graft and pooled TCR clones form the recipient GI tract. Results from 1 representative experiment are shown for total TCR sequences obtained (upper panels) and unique clones (lower panels). T-cell clones from the donor graft were identified as being shared in all, 2, or just 1 recipient group GI tract pooled TCR repertoire at days 9 to 11. A small proportion of the distinct TCR clonal sequences are shared among groups; however, the clones that occur at the most abundant frequency are commonly found across all groups (gray). Distinct donor TCR repertoire can be identified in C57BL6 syngeneic recipients (green), MHC major-mismatched BR10 (red), and BALB/c recipients (purple) or in both major but not syngeneic recipient mice (tan). (B) Sharing of distinct TCR clones among individual recipient mice. A representative transplant experiment is shown (experiment T1; n ≥ 3 mice per group) with degrees of clonal overlap shown by a Venn diagram comparing TCR clones within recipient groups for clones found in any recipient (first row, n = 1), clones found in at least 2 recipients (second row, n = 2), clones found in at least 3 recipients (third row, n = 3), clones found in all recipients within a group (fourth row, n = 3 or 4), and shared clone found across all mice in all transplant recipient groups. The only 1 common clone shared by 3 groups is iNKT CDR3 clone (last row).

General features of TCRA repertoire reconstitution. (A) Sharing of identifiable TCR clones between the donor graft and pooled TCR clones form the recipient GI tract. Results from 1 representative experiment are shown for total TCR sequences obtained (upper panels) and unique clones (lower panels). T-cell clones from the donor graft were identified as being shared in all, 2, or just 1 recipient group GI tract pooled TCR repertoire at days 9 to 11. A small proportion of the distinct TCR clonal sequences are shared among groups; however, the clones that occur at the most abundant frequency are commonly found across all groups (gray). Distinct donor TCR repertoire can be identified in C57BL6 syngeneic recipients (green), MHC major-mismatched BR10 (red), and BALB/c recipients (purple) or in both major but not syngeneic recipient mice (tan). (B) Sharing of distinct TCR clones among individual recipient mice. A representative transplant experiment is shown (experiment T1; n ≥ 3 mice per group) with degrees of clonal overlap shown by a Venn diagram comparing TCR clones within recipient groups for clones found in any recipient (first row, n = 1), clones found in at least 2 recipients (second row, n = 2), clones found in at least 3 recipients (third row, n = 3), clones found in all recipients within a group (fourth row, n = 3 or 4), and shared clone found across all mice in all transplant recipient groups. The only 1 common clone shared by 3 groups is iNKT CDR3 clone (last row).

Close Modal

or Create an Account

Close Modal
Close Modal