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Fig. 1. Isl1 marks a subset of progenitors in heart and limb. (A-H)
Isl1 lineages in heart. Lineage studies with a new Isl1Cre/+ mouse
line give results consistent with those observed utilizing an
Isl1-IRES-Cre mouse line (Srinivas et al., 1999;
Cai et al., 2003). Excision
with the new Isl1Cre/+ occurred more efficiently. Isl1-expressing
progenitors contribute to most cells of the outflow tract, right ventricle and
atria, and also to some cells in the left ventricle (Cai et al., 203).
(I,J) Isl1 lineages in forelimb. Isl1 lineages do not contribute
in any significant number to the forelimbs. (K-U) Isl1 lineages in
hindlimb. A majority of cells in the hindlimb derive from Isl1-expressing
cells. Isl1 cells contribute in an anterior-posterior gradient, with posterior
domains deriving almost entirely from Isl1-expressing lineages. Isl1 lineages
contribute to hindlimb mesoderm, not ectoderm (S-U). (V-G') Isl1
mRNA expression in lateral plate mesoderm adjacent to and within the limb bud.
A comparison of Isl1 mRNA expression to Isl1 lineage results demonstrated that
Isl1 mRNA expression is downregulated as hindlimb progenitors migrate into the
limb. OFT, outflow tract; RV, right ventricle; LV, left ventricle; A,
anterior; P, posterior; Lat, lateral view; Dor, dorsal view; Ven, ventral
view.