TRAFFICKING OF ADOPTIVELY TRANSFERRED B-LYMPHOCYTES IN B-LYMPHOCYTE-DEFICIENT MICE

Authors
Citation
R. Roth et Mj. Mamula, TRAFFICKING OF ADOPTIVELY TRANSFERRED B-LYMPHOCYTES IN B-LYMPHOCYTE-DEFICIENT MICE, Journal of Experimental Biology, 200(14), 1997, pp. 2057-2062
Citations number
15
Categorie Soggetti
Biology
ISSN journal
00220949
Volume
200
Issue
14
Year of publication
1997
Pages
2057 - 2062
Database
ISI
SICI code
0022-0949(1997)200:14<2057:TOATBI>2.0.ZU;2-H
Abstract
Many studies have investigated the fate of adoptively transferred lymp hocytes in recipient mice, although little is known of the sites where these transferred cells reside at particular time points, Using flow cytometry, we analyzed the trafficking pattern of adoptively transferr ed naive B cells into the lymphoid organs of syngeneic B-cell-deficien t (mu MT) mice, Within the first 24 h of transfer, the location of B c ells was highly dependent on the mode of B-cell transfer, When B cells were injected subcutaneously into mu MT mice, they showed a different trafficking pattern from cells administered into the peritoneal cavit y or injected intravenously. After subcutaneous transfer into the thig h, the greatest number of B cells was detected in the popliteal lymph node nearest to the injection site, whereas the lowest number was dete cted in the axillary lymph node opposite to the injection side, Within the first 24 h of either intraperitoneal and intravenous injection, B cells were found in approximately equal numbers in the lymph nodes an d the spleen, Two days later, the B-cell distribution in the lymphoid organs appeared to be independent of the mode of B-cell transfer, A tr ansient decrease in the numbers of splenic and lymph node B cells occu rred 9 days after B-cell transfer (a decrease from 70 to 87 %) prior t o the outgrowth of B cells that occurs 21 days after transfer, These s tudies are useful for understanding the numbers of B cells that may be required in adoptive transfer studies and their potential cellular in teractions at particular physiological sites based on the route of cel l transfer.