Prokineticin-1 (Prok-1) works coordinately with glial cell line-derived neurotrophic factor (GDNF) to mediate proliferation and differentiation of enteric neural crest cells
Autor: | Hiu-Ching Poon, Mai Har Sham, Cathy K.Y. Shum, Vincent C.H. Lui, Paul K.H. Tam, Elly Sau-Wai Ngan, Maria-Mercè Garcia-Barceló |
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Rok vydání: | 2008 |
Předmět: |
medicine.medical_specialty
Mice Transgenic Biology Models Biological Enteric Nervous System Receptors G-Protein-Coupled Mice Neurotrophic factors Internal medicine medicine Glial cell line-derived neurotrophic factor Animals Glial Cell Line-Derived Neurotrophic Factor Molecular Biology Neural crest cell Cell Proliferation Glycoproteins Oligonucleotide Array Sequence Analysis Extracellular Matrix Proteins urogenital system Microarray analysis techniques Gene Expression Profiling Proto-Oncogene Proteins c-ret Gene Expression Regulation Developmental Neural crest Cell Differentiation Cell Biology Prokineticin receptor 1 Embryo Mammalian GDNF Prokineticin Cell biology Endocrinology nervous system Neural Crest biology.protein Vascular Endothelial Growth Factor Endocrine-Gland-Derived Enteric nervous system GDNF family of ligands Prok-1 Vasoactive Intestinal Peptide |
Zdroj: | Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1783:467-478 |
ISSN: | 0167-4889 |
DOI: | 10.1016/j.bbamcr.2007.09.005 |
Popis: | Enteric neural crest cells (NCC) are multipotent progenitors which give rise to neurons and glia of the enteric nervous system (ENS) during fetal development. Glial cell line-derived neurotrophic factor (GDNF)/RET receptor tyrosine kinase (Ret) signaling is indispensable for their survival, migration and differentiation. Using microarray analysis and isolated NCCs, we found that 45 genes were differentially expressed after GDNF treatment (16 h), 29 of them were up-regulated including 8 previously undescribed genes. Prokineticin receptor 1 (PK-R1), a receptor for Prokineticins (Prok), was identified in our screen and shown to be consistently up-regulated by GDNF in enteric NCCs. Further, PK-R1 was persistently expressed at a lower level in the enteric ganglions of the c-Ret deficient mice when compared to that of the wild-type littermates. Subsequent functional analysis showed that GDNF potentiated the proliferative and differentiation effects of Prok-1 by up-regulating PK-R1 expression in enteric NCCs. In addition, expression analysis and gene knock-down experiments indicated that Prok-1 and GDNF signalings shared some common downstream targets. More importantly, Prok-1 could induce both proliferation and expression of differentiation markers of c-Ret deficient NCCs, suggesting that Prok-1 may also provide a complementary pathway to GDNF signaling. Taken together, these findings provide evidence that Prok-1 crosstalks with GDNF/Ret signaling and probably provides an additional layer of signaling refinement to maintain proliferation and differentiation of enteric NCCs. |
Databáze: | OpenAIRE |
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