Figure 6
Figure 6. Role of lymphocytes and the common γ chain for mast cells in KitW/Wv mice. Adoptive transfer of wild-type (R+γ+Kit+/+) splenic lymphocytes into R−γ−KitW/Wv mice (D) lead to approximately 50% reconstitution of circulating T cells compared with Kit+/+ (A) or KitW/Wv (B) mice. Nonreconstituted R−γ−KitW/Wv mice are shown as controls (C). Ears in these groups of mice were subjected to PMA treatment over a period of 6 weeks, and mast cell numbers in treated and untreated ears from all mice were determined by histology (E-H). The differences in mast cell counts comparing untreated (closed symbols) and PMA-treated (open symbols) skin samples had significant one-sided P values (P = .05, Mann-Whitney test) in panels E through H. The P value (.2) comparing the PMA-treated skins in panel G versus panel H was not significant (see text). Kit+/+ were 13-week-old C57BL/6 mice (A,E). KitW/Wv (B,F), noninjected R−γ−KitW/Wv (C,G), and lymphocyte-recipient R−γ−KitW/Wv (D,H) mice were 17 to 20 weeks old. Donors (D,H) were 25-week-old C57BL/6 mice. To determine the possible role of γc for the defective mast cell reconstitution in R−γ−KitW/Wv mice, wild-type (R+γ+Kit+/+) BMMCs were injected repeatedly (see “Material and methods” for cell numbers, frequency of injections, and duration of the experiment) into R−γ−KitW/Wv (J) and KitW/Wv (K) mice. Numbers of mast cells in the spleen, a site that is more effectively colonized than skin following intravenous transfer of BMMCs,33 were determined by flow cytometry in noninjected controls (solid symbols in I-K) and in injected R−γ−KitW/Wv (J) and KitW/Wv (K). Age of the mice was 17 weeks (C57BL/6) (I), 9 to 11 weeks (noninjected R−γ−KitW/Wv) (J), 13 to 30 weeks (BMMC-injected R−γ−KitW/Wv) (J), 21 weeks (noninjected KitW/Wv) (K), and 39 weeks (BMMC-injected KitW/Wv) (K). Mast cells appeared in the spleens of both types of recipients, but their numbers were at least one order of magnitude higher in KitW/Wv compared with R−γ−KitW/Wv. The one-sided P value (.004) of the comparison of the BMMC-injected animals in panel J versus panel K by Mann-Whitney test was significant. Horizontal lines indicate the mean cell number for each group of mice (A-K). Hence, γc-competent mast cells did not rescue the defective mast cell reconstitution in R−γ−KitW/Wv mice.

Role of lymphocytes and the common γ chain for mast cells in KitW/Wv mice. Adoptive transfer of wild-type (R+γ+Kit+/+) splenic lymphocytes into RγKitW/Wv mice (D) lead to approximately 50% reconstitution of circulating T cells compared with Kit+/+ (A) or KitW/Wv (B) mice. Nonreconstituted RγKitW/Wv mice are shown as controls (C). Ears in these groups of mice were subjected to PMA treatment over a period of 6 weeks, and mast cell numbers in treated and untreated ears from all mice were determined by histology (E-H). The differences in mast cell counts comparing untreated (closed symbols) and PMA-treated (open symbols) skin samples had significant one-sided P values (P = .05, Mann-Whitney test) in panels E through H. The P value (.2) comparing the PMA-treated skins in panel G versus panel H was not significant (see text). Kit+/+ were 13-week-old C57BL/6 mice (A,E). KitW/Wv (B,F), noninjected RγKitW/Wv (C,G), and lymphocyte-recipient RγKitW/Wv (D,H) mice were 17 to 20 weeks old. Donors (D,H) were 25-week-old C57BL/6 mice. To determine the possible role of γc for the defective mast cell reconstitution in RγKitW/Wv mice, wild-type (R+γ+Kit+/+) BMMCs were injected repeatedly (see “Material and methods” for cell numbers, frequency of injections, and duration of the experiment) into RγKitW/Wv (J) and KitW/Wv (K) mice. Numbers of mast cells in the spleen, a site that is more effectively colonized than skin following intravenous transfer of BMMCs,33  were determined by flow cytometry in noninjected controls (solid symbols in I-K) and in injected RγKitW/Wv (J) and KitW/Wv (K). Age of the mice was 17 weeks (C57BL/6) (I), 9 to 11 weeks (noninjected RγKitW/Wv) (J), 13 to 30 weeks (BMMC-injected RγKitW/Wv) (J), 21 weeks (noninjected KitW/Wv) (K), and 39 weeks (BMMC-injected KitW/Wv) (K). Mast cells appeared in the spleens of both types of recipients, but their numbers were at least one order of magnitude higher in KitW/Wv compared with RγKitW/Wv. The one-sided P value (.004) of the comparison of the BMMC-injected animals in panel J versus panel K by Mann-Whitney test was significant. Horizontal lines indicate the mean cell number for each group of mice (A-K). Hence, γc-competent mast cells did not rescue the defective mast cell reconstitution in RγKitW/Wv mice.

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