Development and fibronectin signaling requirements of the zebrafish interrenal vessel
- Authors
- Chiu, C.H., Chou, C.W., Takada, S., and Liu, Y.W.
- ID
- ZDB-PUB-120905-5
- Date
- 2012
- Source
- PLoS One 7(8): e43040 (Journal)
- Registered Authors
- Liu, Yi-wen, Takada, Shinji
- Keywords
- none
- MeSH Terms
-
- Animals
- Fibronectins/genetics
- Fibronectins/metabolism*
- Immunohistochemistry
- In Situ Hybridization
- Interrenal Gland/blood supply*
- Interrenal Gland/embryology
- Signal Transduction/genetics
- Signal Transduction/physiology
- Zebrafish
- Zebrafish Proteins/genetics
- Zebrafish Proteins/metabolism*
- PubMed
- 22937010 Full text @ PLoS One
Background
The early morphogenetic steps of zebrafish interrenal tissue, the teleostean counterpart of the mammalian adrenal gland, are modulated by the peri-interrenal angioblasts and blood vessels. While an organized distribution of intra-adrenal vessels and extracellular matrix is essential for the fetal adrenal cortex remodeling, whether and how an intra-interrenal buildup of vasculature and extracellular matrix forms and functions during interrenal organogenesis in teleosts remains unclear.
Methodology and Principal Findings
We characterized the process of interrenal gland vascularization by identifying the interrenal vessel (IRV); which develops from the axial artery through angiogenesis and is associated with highly enriched Fibronectin (Fn) accumulation at its microenvironment. The loss of Fn1 by either antisense morpholino (MO) knockdown or genetic mutation inhibited endothelial invasion and migration of the steroidogenic tissue. The accumulation of peri-IRV Fn requires Integrin α5 (Itga5), with its knockdown leading to interrenal and IRV morphologies phenocopying those in the fn1 morphant and mutant. fn1b, another known fn gene in zebrafish, is however not involved in the IRV formation. The distribution pattern of peri-IRV Fn could be modulated by the blood flow, while a lack of which altered angiogenic direction of the IRV as well as its ability to integrate with the steroidogenic tissue. The administration of Fn antagonist through microangiography exerted reducing effects on both interrenal vessel angiogenesis and steroidogenic cell migration.
Conclusions and Significance
This work is the first to identify the zebrafish IRV and to characterize how its integration into the developing interrenal gland requires the Fn-enriched microenvironment, which leads to the possibility of using the IRV formation as a platform for exploring organ-specific angiogenesis. In the context of other developmental endocrinology studies, our results indicate a highly dynamic interrenal-vessel interaction immediately before the onset of stress response in the zebrafish embryo.