TY - JOUR
T1 - Marked reduction of mouse peritoneal CD5+ B cells by intraperitoneal administration of lipopolysaccharide
AU - Paeng, Noriko
AU - Kido, Nobuo
AU - Kato, Yutaka
AU - Sugiyama, Tsuyoshi
AU - Koide, Naoki
AU - Naruse, Makoto
AU - Jiang, Guo Zhi
AU - Lwin, Tint
AU - Yoshida, Tomoaki
AU - Yokochi, Takashi
PY - 1997/1
Y1 - 1997/1
N2 - Intraperitoneal administration of lipopolysaccharide to mice induced a marked reduction of CD5+ B cells in the peritoneal cavity. The reduction was not induced by intravenous, subcutaneous, or oral administration of lipopolysaccharide. The reduction continued for about 10 days after the injection, and the CD5+ B-cell count recovered to the normal state about 14 days after the injection. The reduction of peritoneal CD5+ B cells might be caused by apoptotic cell death. Injection of lipopolysaccharide did not result in production of antibody to lipopolysaccharide. On the other hand, intraperitoneal injection of heat-killed bacteria did not induce a reduction of peritoneal CD5+ B cells and elicited the definite production of antibody to lipopolysaccharide.
AB - Intraperitoneal administration of lipopolysaccharide to mice induced a marked reduction of CD5+ B cells in the peritoneal cavity. The reduction was not induced by intravenous, subcutaneous, or oral administration of lipopolysaccharide. The reduction continued for about 10 days after the injection, and the CD5+ B-cell count recovered to the normal state about 14 days after the injection. The reduction of peritoneal CD5+ B cells might be caused by apoptotic cell death. Injection of lipopolysaccharide did not result in production of antibody to lipopolysaccharide. On the other hand, intraperitoneal injection of heat-killed bacteria did not induce a reduction of peritoneal CD5+ B cells and elicited the definite production of antibody to lipopolysaccharide.
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U2 - 10.1128/iai.65.1.122-126.1997
DO - 10.1128/iai.65.1.122-126.1997
M3 - Article
C2 - 8975901
AN - SCOPUS:14444279914
SN - 0019-9567
VL - 65
SP - 122
EP - 126
JO - Infection and Immunity
JF - Infection and Immunity
IS - 1
ER -