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Asymmetric T Lymphocyte Division in the Initiation of Adaptive Immune Responses
Oleh:
Chang, John T.
;
Palanivel, Vikram R.
;
Kinjyo, Ichiko
;
Schambach, Felix
;
Intlekofer, Andrew M
;
Banerjee, Arnob
;
Longworth, Sarah A.
;
Vinup, Kristine E.
;
Mrass, Paul
;
Oliaro, Jane
;
Kileen, Nigel
;
Orange, Jordan S.
;
Russell, Sara M.
;
Weninger, Wolfgang
;
Reiner, Steven L.
Jenis:
Article from Bulletin/Magazine
Dalam koleksi:
SCIENCE (keterangan: ada di Proquest) vol. 315 no. 5819 (Mar. 2007)
,
page 1687.
Topik:
Immunology
Ketersediaan
Perpustakaan FK
Nomor Panggil:
S01.K.2007.03
Non-tandon:
1 (dapat dipinjam: 0)
Tandon:
tidak ada
Lihat Detail Induk
Isi artikel
A hallmark of mammalian immunity is the heterogeneity of cell fate that exists among pathogen experienced lymphocytes. We show that a dividing T lymphocyte initially responding to a microbE exhibits unequal partitioning of proteins that mediate signaling, cell fate specification, and asymmetric cell division. Asymmetric segregation of determinants appears to be coordinated by prolonged interaction between the T cell and its antigen-presenting cell before division. Additionally, the first two daughter T cells displayed phenotypic and functional indicators of bein~ differentially fated toward effector and memory lineages. These results suggest a mechanism by which a single lymphocyte can apportion diverse cell fates necessary for adaptive immunity.
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