Sel T Regulator CD4+CD25+ Mencegah Terjadinya Fenotip Letal pada Mencit Defisiensi CD122
Mice with a deficiency of cluster of differentiation/CD122 molecules experience increased memory Tcells. Increased memory T cells are activated and interfered with homeostasis that cause death at the ageof 10 ~ 12 weeks. To clarify whether the expression of CD25 molecules on CD4+ T cells responsible...
| 發表在: | Jurnal Veteriner |
|---|---|
| Main Authors: | , |
| 格式: | Article |
| 語言: | 英语 |
| 出版: |
Universitas Udayana
2012-11-01
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| 主題: | |
| 在線閱讀: | http://ojs.unud.ac.id/index.php/jvet/article/view/3498 |
| _version_ | 1857084812857180160 |
|---|---|
| author | Muhaimin Rifa’i Widodo - |
| author_facet | Muhaimin Rifa’i Widodo - |
| author_sort | Muhaimin Rifa’i |
| collection | DOAJ |
| container_title | Jurnal Veteriner |
| description | Mice with a deficiency of cluster of differentiation/CD122 molecules experience increased memory Tcells. Increased memory T cells are activated and interfered with homeostasis that cause death at the ageof 10 ~ 12 weeks. To clarify whether the expression of CD25 molecules on CD4+ T cells responsible for thedevelopment of lethal phenotypes in CD122-/- mice, we did a transfusion of CD4+CD25+ T cells from normalmice to CD122-/- neonates. Transfusion of purified CD4+CD25+ T cells as much as 3 x 104 can prevent theoccurrence of lethal phenotypes generally experienced by CD122-/- mice. Transfusion of CD4+CD25+ T cellsin CD122-/- neonates cause all of the abnormalities that occur in T cell and leukocyte cells can be preventedand develop into normal. Similarly, the hematocrit that decreased dramatically in CD122-/- mice candevelop normally after receiving a transfusion of CD4+CD25+ T cells. In contras, transfusion of CD4+CD25-T cells in CD122-/- mice did not have the effect of preventing the development of the abnormalities inCD122-/- mice. CD4+CD25+ T cells that are lost in periphery of CD122-/- mice can restore to normal afterreceiving a transfusion of CD4+CD25+ T cells. These results clearly show that the expression of IL-2R?(CD25) on CD4+ T cells become pre-requisite for CD4 T cell population in order to play a role as regulatorcells. |
| format | Article |
| id | doaj-art-bc306d188cd84d9f8a8f000bbdb8d24d |
| institution | Directory of Open Access Journals |
| issn | 1411-8327 2477-5665 |
| language | English |
| publishDate | 2012-11-01 |
| publisher | Universitas Udayana |
| record_format | Article |
| spelling | doaj-art-bc306d188cd84d9f8a8f000bbdb8d24d2025-08-19T19:21:00ZengUniversitas UdayanaJurnal Veteriner1411-83272477-56652012-11-011233324Sel T Regulator CD4+CD25+ Mencegah Terjadinya Fenotip Letal pada Mencit Defisiensi CD122Muhaimin Rifa’iWidodo -Mice with a deficiency of cluster of differentiation/CD122 molecules experience increased memory Tcells. Increased memory T cells are activated and interfered with homeostasis that cause death at the ageof 10 ~ 12 weeks. To clarify whether the expression of CD25 molecules on CD4+ T cells responsible for thedevelopment of lethal phenotypes in CD122-/- mice, we did a transfusion of CD4+CD25+ T cells from normalmice to CD122-/- neonates. Transfusion of purified CD4+CD25+ T cells as much as 3 x 104 can prevent theoccurrence of lethal phenotypes generally experienced by CD122-/- mice. Transfusion of CD4+CD25+ T cellsin CD122-/- neonates cause all of the abnormalities that occur in T cell and leukocyte cells can be preventedand develop into normal. Similarly, the hematocrit that decreased dramatically in CD122-/- mice candevelop normally after receiving a transfusion of CD4+CD25+ T cells. In contras, transfusion of CD4+CD25-T cells in CD122-/- mice did not have the effect of preventing the development of the abnormalities inCD122-/- mice. CD4+CD25+ T cells that are lost in periphery of CD122-/- mice can restore to normal afterreceiving a transfusion of CD4+CD25+ T cells. These results clearly show that the expression of IL-2R?(CD25) on CD4+ T cells become pre-requisite for CD4 T cell population in order to play a role as regulatorcells.http://ojs.unud.ac.id/index.php/jvet/article/view/3498CD4+CD25+, sel T regulator, CD122-/- |
| spellingShingle | Muhaimin Rifa’i Widodo - Sel T Regulator CD4+CD25+ Mencegah Terjadinya Fenotip Letal pada Mencit Defisiensi CD122 CD4+CD25+, sel T regulator, CD122-/- |
| title | Sel T Regulator CD4+CD25+ Mencegah Terjadinya Fenotip Letal pada Mencit Defisiensi CD122 |
| title_full | Sel T Regulator CD4+CD25+ Mencegah Terjadinya Fenotip Letal pada Mencit Defisiensi CD122 |
| title_fullStr | Sel T Regulator CD4+CD25+ Mencegah Terjadinya Fenotip Letal pada Mencit Defisiensi CD122 |
| title_full_unstemmed | Sel T Regulator CD4+CD25+ Mencegah Terjadinya Fenotip Letal pada Mencit Defisiensi CD122 |
| title_short | Sel T Regulator CD4+CD25+ Mencegah Terjadinya Fenotip Letal pada Mencit Defisiensi CD122 |
| title_sort | sel t regulator cd4 cd25 mencegah terjadinya fenotip letal pada mencit defisiensi cd122 |
| topic | CD4+CD25+, sel T regulator, CD122-/- |
| url | http://ojs.unud.ac.id/index.php/jvet/article/view/3498 |
| work_keys_str_mv | AT muhaiminrifai seltregulatorcd4cd25mencegahterjadinyafenotipletalpadamencitdefisiensicd122 AT widodo seltregulatorcd4cd25mencegahterjadinyafenotipletalpadamencitdefisiensicd122 |
