TY - JOUR
T1 - Natural Occurrence of Nuc in the Sera of Autoimmune-Prone MRL/lpr Mice
AU - Kanai, Yoshiyuki
AU - Miura, Keiji
AU - Uehara, Takemi
AU - Amagai, Mieko
AU - Takeda, Osamu
AU - Tanuma, Sei Ichi
AU - Kurosawa, Yoshikazu
PY - 1993/10/29
Y1 - 1993/10/29
N2 - We previously established a clone of cells termed KML1-7 which produces a soluble factor that boosts anti-DNA antibody production both in vitro and in vivo across the H-2 barrier. By using the purified protein, termed nucleobindin (Nuc), we cloned cDNA and produced recombinant (r) Nuc in E.coli. Although the purified rNuc showed biological activities such as anti-DNA antibody boosting and DNA binding, there was no evidence that Nuc is really associated with autoimmune status in lupus-prone MRL/lpr mice. Here we report that identification of Nuc was successful from the sera of MRL/lpr mice, but not from those of the substrain MRL/n mice, which show no apparent autoimmune syndrome at the same age of MRL/lpr mice, by means of immunochemical as well as N-terminal amino-acid sequencing methods.
AB - We previously established a clone of cells termed KML1-7 which produces a soluble factor that boosts anti-DNA antibody production both in vitro and in vivo across the H-2 barrier. By using the purified protein, termed nucleobindin (Nuc), we cloned cDNA and produced recombinant (r) Nuc in E.coli. Although the purified rNuc showed biological activities such as anti-DNA antibody boosting and DNA binding, there was no evidence that Nuc is really associated with autoimmune status in lupus-prone MRL/lpr mice. Here we report that identification of Nuc was successful from the sera of MRL/lpr mice, but not from those of the substrain MRL/n mice, which show no apparent autoimmune syndrome at the same age of MRL/lpr mice, by means of immunochemical as well as N-terminal amino-acid sequencing methods.
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U2 - 10.1006/bbrc.1993.2310
DO - 10.1006/bbrc.1993.2310
M3 - Article
C2 - 8240349
AN - SCOPUS:0027482974
SN - 0006-291X
VL - 196
SP - 729
EP - 736
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -