TY - JOUR
T1 - Regulation of primitive hematopoiesis in zebrafish embryos by the death receptor gene
AU - Kwan, Tommy T.
AU - Liang, Raymond
AU - Verfaillie, Catherine M.
AU - Ekker, Stephen C.
AU - Chan, Li C.
AU - Lin, Shuo
AU - Leung, Anskar Y.H.
N1 - Funding Information:
We thanked Mr. Howard C. H. Chow for performing the reverse transcriptase polymerase chain reaction experiments. Work was supported by RGC grant (HKU 7488/04M).
PY - 2006/1
Y1 - 2006/1
N2 - Objective. We investigated the regulatory mechanism of primitive hematopoiesis in zebrafish (Danio rerio) embryos with particular reference to the role of a death receptor (zDR) gene, based on a morpholino (MO) knockdown approach. Methods. MOs targeting the zDR and chordin (Chd) were injected into naturally spawned embryos at one- to four-cell stage. A random sequence (RS) MO was used as a control. Effects on hemoglobin formation (Hb), apoptosis, and lineage-specific gene expression were examined. Embryos injected with zDR, Chd, and RS-MOs were denoted zDRmo, zChdmo, and zRS mo, respectively. Those coinjected with Chd+zDR-MOs and Chd+RS-MOs were abbreviated zChd+DRmo and zChd+RSmo. Results. zDR mRNA expression was restricted to the intermediate cell mass of wild-type (WT) and zChdmo embryos. At 48 hours postfertilization, zDRmo embryos showed increased Hb compared with WT or zRSmo embryos (2.36 × 10-2 ± 1.13 × 10-3 vs 1.85 × 10-2 ± 5.60 × 10-4 vs 1.79 × 10 -2 ± 1.31 × 10-3 U, p < 0.05). zChd+DRmo embryos also showed increased Hb compared with zChd mo or zChd+RSmo embryos (4.60 × 10-2 ± 2.79 × 10-3 vs 3.17 × 10-2 ± 1.07 × 10-3 vs 3.05 × 10-2 ± 1.25 × 10-3 U, p < 0.05). zDR-MO reduced apoptosis, as shown by reduced terminal transferase-mediated dUTP nick end-labeling staining in zChd+DRmo compared with zChd+RSmo embryos and caspase-3 activity in zDRmo vs zRSmo (0.525 ± 0.094 vs 0.953 ± 0.113 U, p < 0.05), and zChd+DRmo vs zChd+RSmo embryos (0.247 ± 0.121 vs 1.180 ± 0.082, p < 0.05). zChd+DRmo embryos showed upregulation of erythroid-specific embryonic hemoglobin gene expression but not that of a myeloid-specific myeloperoxidase gene. Conclusion. Knockdown of zDR in zebrafish embryos decreased apoptosis and increased Hb, suggesting that zDR may regulate primitive hematopoiesis during development.
AB - Objective. We investigated the regulatory mechanism of primitive hematopoiesis in zebrafish (Danio rerio) embryos with particular reference to the role of a death receptor (zDR) gene, based on a morpholino (MO) knockdown approach. Methods. MOs targeting the zDR and chordin (Chd) were injected into naturally spawned embryos at one- to four-cell stage. A random sequence (RS) MO was used as a control. Effects on hemoglobin formation (Hb), apoptosis, and lineage-specific gene expression were examined. Embryos injected with zDR, Chd, and RS-MOs were denoted zDRmo, zChdmo, and zRS mo, respectively. Those coinjected with Chd+zDR-MOs and Chd+RS-MOs were abbreviated zChd+DRmo and zChd+RSmo. Results. zDR mRNA expression was restricted to the intermediate cell mass of wild-type (WT) and zChdmo embryos. At 48 hours postfertilization, zDRmo embryos showed increased Hb compared with WT or zRSmo embryos (2.36 × 10-2 ± 1.13 × 10-3 vs 1.85 × 10-2 ± 5.60 × 10-4 vs 1.79 × 10 -2 ± 1.31 × 10-3 U, p < 0.05). zChd+DRmo embryos also showed increased Hb compared with zChd mo or zChd+RSmo embryos (4.60 × 10-2 ± 2.79 × 10-3 vs 3.17 × 10-2 ± 1.07 × 10-3 vs 3.05 × 10-2 ± 1.25 × 10-3 U, p < 0.05). zDR-MO reduced apoptosis, as shown by reduced terminal transferase-mediated dUTP nick end-labeling staining in zChd+DRmo compared with zChd+RSmo embryos and caspase-3 activity in zDRmo vs zRSmo (0.525 ± 0.094 vs 0.953 ± 0.113 U, p < 0.05), and zChd+DRmo vs zChd+RSmo embryos (0.247 ± 0.121 vs 1.180 ± 0.082, p < 0.05). zChd+DRmo embryos showed upregulation of erythroid-specific embryonic hemoglobin gene expression but not that of a myeloid-specific myeloperoxidase gene. Conclusion. Knockdown of zDR in zebrafish embryos decreased apoptosis and increased Hb, suggesting that zDR may regulate primitive hematopoiesis during development.
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U2 - 10.1016/j.exphem.2005.09.017
DO - 10.1016/j.exphem.2005.09.017
M3 - Article
C2 - 16413388
AN - SCOPUS:30344457882
SN - 0301-472X
VL - 34
SP - 27
EP - 34
JO - Experimental Hematology
JF - Experimental Hematology
IS - 1
ER -