A novel leukemia cell gro-th-promoting activity has been identified in
the culture supernatant from a human B cell leukemia cell line, BALL-
1. The supernatant from unstimulated cultures or the BALL-1 cells sign
ificantly pro-ted the growth of 16 out of 24 leukemia/lymphoma cell li
nes of different lineages (T, B and non-lymphoid) in a minimal concent
ration of fetal bovine serum (FBS), and of 5 out of 12 cases of fresh
leukemia cells in FBS-free medium. The growth-promoting activity in th
e BALL-1 supernatant has been further characterized using FPLC chromat
ography, molecular weight (MW) sieve filtration and dialysts. The MW o
f the factor was less than 10 kDa. The growth-promoting activity was h
eat and acid stable and resistant to trypsin treatment. The factor iso
lated from the BALL-1 supernatant was distinct from known polypeptide
growth factors with MW below 10 kDa, such as epidermal growth factor,
transforming growth factor alpha, insulin-like growth factor I (IGF-I)
, IGF-II and insulin, as determined by specific antibodies and by cell
growth-promoting tests. The factor in the BALL-1 supernatant did not
promote the proliferation of normal human fresh peripheral blood lymph
ocytes or mouse fibroblast cell line, BALB/c 3T3. In addition to the B
ALL-1 supernatant, a similar growth-promoting activity was found in th
e culture supernatants from 13 of 17 leukemia/lymphoma cell lines test
ed. The activity in these culture supernatants promoted the growth of
leukemia/lymphoma cell lines in autocrine and/or paracrine fashions. T
hese observations suggest that the low MW cell growth-promoting activi
ty found in the BALL-1 culture supernatant is mediated by a novel fact
or which may well be responsible for the clonal expansion of particula
r leukemic clones.