Transforming growth factor-beta (TGF-beta) superfamily members and the
ir cell-surface receptors may play inductive and/or regulatory roles i
n tooth development and repair. It will be important to identify the c
omplete set of TGF-beta superfamily receptors, to examine their tempor
al and spatial localization during tooth development, and to elucidate
the cascade of molecular events of tooth formation induced by the TGF
-beta superfamily. In this report, we have cloned the cDNAs encoding p
otential receptors for TGF-beta superfamily members in rat incisor pul
p and bovine adult pulp which are regarded as embryonic and adult pulp
, respectively. We analyzed poly (A)(+) RNA from rat incisor pulp and
bovine adult pulp by reverse-transcriptase/polymerase chain-reaction (
RT-PCR), using degenerate primers corresponding to the most conserved
amino acid sequences in the intracellular serine/threonine kinase of t
ype I or type II receptors. Each amplified cDNA encoding activin recep
torlike kinase-l (ALK-1), ALK-2, ALK-3 (bone morphogenetic protein rec
eptor type IA, BMPR-IA), ALK-4 (B1), ALK-5, ALK-6 (BMPR-IB), and BMPR-
II (BMP type II receptor) was found to be in dental pulp. Northern blo
t analysis further detected TGF-beta type II receptor (T beta R-II) mR
NA transcript in addition to the above-identified receptors. These res
ults provide the first evidence of multiple type I and type II recepto
rs for TGF-beta s, activins, and BMPs expressed in embryonic and adult
pulp, implicating diverse function in tooth development and pulp tiss
ue repair.