TY - JOUR
T1 - Islet1 cardiovascular progenitors
T2 - A single source for heart lineages?
AU - Laugwitz, Karl Ludwig
AU - Moretti, Alessandra
AU - Caron, Leslie
AU - Nakano, Atsushi
AU - Chien, Kenneth R.
PY - 2008/1
Y1 - 2008/1
N2 - The creation of regenerative stem cell therapies for heart disease requires that we understand the molecular mechanisms that govern the fates and differentiation of the diverse muscle and non-muscle cell lineages of the heart. Recently, different cardiac cell types have been reported to arise from a common, multipotent Islet1 (lsl1)-positive progenitor, suggesting that a clonal model of heart lineage diversification might occur that is analogous to hematopoiesis. The ability to isolate, renew and differentiate lsl1+ precursors from postnatal and embryonic hearts and from embryonic stem cells provides a powerful cell-based system for characterizing the signaling pathways that control cardiovascular progenitor formation, renewal, lineage specification and conversion to specific differentiated progeny.
AB - The creation of regenerative stem cell therapies for heart disease requires that we understand the molecular mechanisms that govern the fates and differentiation of the diverse muscle and non-muscle cell lineages of the heart. Recently, different cardiac cell types have been reported to arise from a common, multipotent Islet1 (lsl1)-positive progenitor, suggesting that a clonal model of heart lineage diversification might occur that is analogous to hematopoiesis. The ability to isolate, renew and differentiate lsl1+ precursors from postnatal and embryonic hearts and from embryonic stem cells provides a powerful cell-based system for characterizing the signaling pathways that control cardiovascular progenitor formation, renewal, lineage specification and conversion to specific differentiated progeny.
UR - http://www.scopus.com/inward/record.url?scp=38949168086&partnerID=8YFLogxK
U2 - 10.1242/dev.001883
DO - 10.1242/dev.001883
M3 - Review article
C2 - 18156162
AN - SCOPUS:38949168086
SN - 0950-1991
VL - 135
SP - 193
EP - 205
JO - Development (Cambridge)
JF - Development (Cambridge)
IS - 2
ER -