A novel alpha-chemokine, designated KS1, was identified from an EST databas
e of a murine immature keratinocyte cDNA library. The ESI has 94% similarit
y to a recently cloned human gene, BRAK, that has no demonstrated function.
Northern analysis of mouse and human genes showed detectable mRNA in brain
, intestine, muscle and kidney. Tumour panel blots showed that BRAK was dow
n-regulated in cervical adenocarcinoma and uterine leiomyoma, but was up-re
gulated in breast invasive ductal carcinoma. KS1 bound specifically to a ce
lls and macrophages, as well as two a cell lines, CESS and A20, and a monoc
yte line, THP-1, KS1 showed no binding to naive or activated T cells. In ad
dition, KS1 stimulated the chemotaxis of CESS and THP-1 cells but not T cel
ls. The s.c. injection of KS1 creates a mixed inflammatory response in Nude
and C3H/HeJ mice. The above data indicates that KS1 and its human homologu
e represents a novel non-ELR a-chemokine that may have important roles in t
rafficking of a cells and monocytes, We propose the name a cell- and monocy
te-activating chemokine (BMAC) for this molecule to reflect the described b
iological functions.