2000
DOI: 10.1002/(sici)1097-0177(200005)218:1<123::aid-dvdy11>3.0.co;2-6
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The rostro-caudal position of cardiac myocytes affect their fate

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Cited by 21 publications
(19 citation statements)
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“…Using different techniques, several investigators established that cardiac AP fates are specified between HH4-7 and determined around HH7-8 (Orts Llorca and Collado, 1967;Satin et al, 1988;Inagaki et al, 1993;Yutzey et al, 1995;Patwardhan et al, 2000). We extend these findings by showing, through reciprocal manipulations of RA signalling, that cardiac AP fates remain plastic from HH4-7, but not after HH8.…”
Section: Gata4 As a Marker For The Early Cardiac Fieldsupporting
confidence: 66%
See 1 more Smart Citation
“…Using different techniques, several investigators established that cardiac AP fates are specified between HH4-7 and determined around HH7-8 (Orts Llorca and Collado, 1967;Satin et al, 1988;Inagaki et al, 1993;Yutzey et al, 1995;Patwardhan et al, 2000). We extend these findings by showing, through reciprocal manipulations of RA signalling, that cardiac AP fates remain plastic from HH4-7, but not after HH8.…”
Section: Gata4 As a Marker For The Early Cardiac Fieldsupporting
confidence: 66%
“…However, the putative contribution of this early RA signalling to cardiac AP patterning needs to be evaluated in the light of previous work indicating that cardiac cells commit irreversibly to their AP phenotypes between stages HH7 and 8, but not earlier (Orts-Llorca and Collado, 1967;Satin et al, 1988;Inagaki et al, 1993;Yutzey et al, 1995;Patwardhan et al, 2000) (for a review, see Xavier-Neto et al, 2001). Therefore, although earlier RA signalling by enzymes other than RALDH2 may play a major role in cardiac development and be necessary or permissive for induction of RALDH2 in the appropriate regions of the cardiogenic plate, the data available indicate that the crucial decision between anterior or posterior fates occurs at developmental times when RALDH2 is the only RALDH enzyme expressed in a clear AP pattern in the cardiac mesoderm.…”
Section: Discussionmentioning
confidence: 99%
“…Chicken and mouse embryo studies indicated that retinoid signaling regulates the fate specification of inflow and out-flow track tissues [17][18][19][20][21][22]. Therefore, we hypothesized that the activation or inactivation of retinoid signaling directs the atrial vs. ventricular fate specification of differentiated hESC cardiac progenitors, and such a mechanism could be used to efficiently generate either hESC-derived atrial-or ventricular-like myocytes.…”
Section: Alternative Retinoid Signals Direct the Differentiation Of Hmentioning
confidence: 99%
“…RA signaling also regulates anterior-posterior polarisation of the heart [17]. Chicken transplantation studies have revealed that the cardiogenic mesoderm from HH stages 4-6, originally fated to be atria, is competent to develop into functional ventricles, and vice versa [18,19]. RA treatment of HH stage 4 cardiogenic tissue activates the expression of the atrium-specific gene AMHC1 in anterior progenitors fated to develop into out-flow track tissues [20].…”
Section: Introductionmentioning
confidence: 99%
“…AMHC1) and posterior region expressing ventricular marker (i.e. VMHC1) [284]. Inhibition of RA signaling in specific time interval during mouse and chicken development (i.e.…”
Section: Signaling Pathways Underlying Cardiac Differentiationmentioning
confidence: 99%