Lymphoproliferative activities produced by cloned thymic myoid cell 87
1207B were analysed by immunological and biochemical methods. The lymp
hoproliferative activities were separated into two fractions by DEAE-S
epharose CL-6B chromatography: one is in the fraction passed through t
he column and the other in the fraction eluated from the column with a
low concentration of NaCl. The eluated fraction induced the prolifera
tion of interleukin-1 (IL-1)-dependent D10N4 M cells. This activity wa
s abrogated by an anti-IL-1 alpha antibody, but not an anti-IL-1 beta
antibody. Expression of IL-1 alpha mRNA was also detected in 871207B c
ells. The thymocyte proliferative activity found in the fraction passe
d through the DEAE-Sepharose column was further separated into three f
ractions by heparin-Sepharose column chromatography: (1) the fraction
passed through the column, (2) the fraction weakly bound to the column
, and (3) the fraction firmly bound to the heparin column. The fractio
n passed through the heparin column sustained the growth of IL-6-depen
dent MH60 . BSF-2 cells. IL-6-specific mRNA was found in 871207B cells
. The thymocyte proliferative activity of the fraction firmly bound to
the heparin column was neutralized with an anti-IL-7 antibody. The bi
ological activity of the fraction weakly bound to the column remained
to be elucidated. These results suggest that thymic myoid cells produc
e IL-1 alpha, IL-6, IL-7 and unidentified lympho-stimulatory factors,
all of which play significant roles in many steps of T-cell developmen
t in the thymus.