Islet1 Derivatives in the Heart Are of Both Neural Crest and Second Heart Field Origin
0303 health sciences
Myocardium
Stem Cells
Green Fluorescent Proteins
LIM-Homeodomain Proteins
Heart
Mice, Transgenic
Wnt1 Protein
Mice
03 medical and health sciences
Neural Crest
Models, Animal
Animals
Cell Lineage
Biomarkers
Transcription Factors
DOI:
10.1161/circresaha.112.266510
Publication Date:
2012-03-07T05:17:11Z
AUTHORS (7)
ABSTRACT
Rationale:
Islet1
(
Isl1
) has been proposed as a marker of cardiac progenitor cells derived from the second heart field and is utilized to identify and purify cardiac progenitors from murine and human specimens for ex vivo expansion. The use of
Isl1
as a specific second heart field marker is dependent on its exclusion from other cardiac lineages such as neural crest.
Objective:
Determine whether
Isl1
is expressed by cardiac neural crest.
Methods and Results:
We used an intersectional fate-mapping system using the
RC
::FrePe allele, which reports dual Flpe and Cre recombination. Combining
Isl1
Cre
/+
, a SHF driver, and
Wnt1
::Flpe, a neural crest driver, with
Rc
::FrePe reveals that some
Isl1
derivatives in the cardiac outflow tract derive from
Wnt1
-expressing neural crest progenitors. In contrast, no overlap was observed between
Wnt1
-derived neural crest and an alternative second heart field driver,
Mef2c-AHF-Cre
.
Conclusions:
Isl1
is not restricted to second heart field progenitors in the developing heart but also labels cardiac neural crest. The intersection of
Isl1
and
Wnt1
lineages within the heart provides a caveat to using
Isl1
as an exclusive second heart field cardiac progenitor marker and suggests that some
Isl1
-expressing progenitor cells derived from embryos, embryonic stem cultures, or induced pluripotent stem cultures may be of neural crest lineage.
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