کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2041041 | 1073141 | 2012 | 13 صفحه PDF | دانلود رایگان |

SummaryHigh-affinity antibodies are generated in germinal centers in a process involving mutation and selection of B cells. Information processing in germinal center reactions has been investigated in a number of recent experiments. These have revealed cell migration patterns, asymmetric cell divisions, and cell-cell interaction characteristics, used here to develop a theory of germinal center B cell selection, division, and exit (the LEDA model). According to this model, B cells selected by T follicular helper cells on the basis of successful antigen processing always return to the dark zone for asymmetric division, and acquired antigen is inherited by one daughter cell only. Antigen-retaining B cells differentiate to plasma cells and leave the germinal center through the dark zone. This theory has implications for the functioning of germinal centers because compared to previous models, high-affinity antibodies appear one day earlier and the amount of derived plasma cells is considerably larger.
Graphical AbstractFigure optionsDownload as PowerPoint slideHighlights
► A model for selecting high-affinity antibodies in the germinal center is derived
► B cell recycling is the dominant pathway of selected B cells
► B cells leave the germinal center through the dark zone
► Asymmetric division determines the fate of germinal center B cells
Journal: - Volume 2, Issue 1, 26 July 2012, Pages 162–174