PUBLICATION
The Kunitz-type serine protease inhibitor Spint2 is required for cellular cohesion, coordinated cell migration and cell survival during zebrafish hatching gland development
- Authors
- Hatzold, J., Wessendorf, H., Pogoda, H.M., Bloch, W., Hammerschmidt, M.
- ID
- ZDB-PUB-210409-12
- Date
- 2021
- Source
- Developmental Biology 476: 148-170 (Journal)
- Registered Authors
- Hammerschmidt, Matthias, Hatzold, Julia, Pogoda, Hans-Martin
- Keywords
- Cell death, Cohesion, Collective cell migration, E-cadherin, Hatching gland, Morphogenesis, Spint2, Zebrafish
- MeSH Terms
-
- Animals
- Epidermis/metabolism
- Cell Survival/physiology
- Membrane Glycoproteins/genetics
- Membrane Glycoproteins/metabolism
- Zebrafish/embryology
- Cadherins
- Serine Proteinase Inhibitors/genetics
- Serine Proteinase Inhibitors/metabolism*
- Gene Expression/genetics
- Cell Adhesion Molecules/genetics
- Gene Expression Regulation, Developmental/genetics
- Cell Movement/physiology
- Proteinase Inhibitory Proteins, Secretory/genetics*
- Proteinase Inhibitory Proteins, Secretory/metabolism
- Cell Adhesion/genetics
- Cell Adhesion/physiology*
- Epithelial Cells/metabolism
- Membrane Proteins/genetics
- Membrane Proteins/metabolism
- Zebrafish Proteins/genetics
- Zebrafish Proteins/metabolism
- Organogenesis
- PubMed
- 33826923 Full text @ Dev. Biol.
Citation
Hatzold, J., Wessendorf, H., Pogoda, H.M., Bloch, W., Hammerschmidt, M. (2021) The Kunitz-type serine protease inhibitor Spint2 is required for cellular cohesion, coordinated cell migration and cell survival during zebrafish hatching gland development. Developmental Biology. 476:148-170.
Abstract
We have previously shown that the Kunitz-type serine protease inhibitor Spint1a, also named Hai1a, is required in the zebrafish embryonic epidermis to restrict the activity of the type II transmembrane serine protease (TTSP) Matriptase1a/St14a, thereby ensuring epidermal homeostasis. A closely related Kunitz-type inhibitor is Spint2/Hai2, which in mammals plays multiple developmental roles that are either redundant or non-redundant with those of Spint1. However, the molecular bases for these non-redundancies are not fully understood. Here, we study spint2 during zebrafish development. It is co-expressed with spint1a in multiple embryonic epithelia, including the outer/peridermal layer of the epidermis. However, unlike spint1a, spint2 expression is absent from the basal epidermal layer but present in hatching gland cells. Hatching gland cells derive from the mesendodermal prechordal plate, from where they undergo a thus far undescribed transit into, and coordinated sheet migration within, the interspace between the outer and basal layer of the epidermis to reach their final destination on the yolk sac. Hatching gland cells usually survive their degranulation that drives embryo hatching but die several days later. In spint2 mutants, cohesion among hatching gland cells and their collective intra-epidermal migration are disturbed, leading to a discontinuous organization of the gland. In addition, cells undergo precocious cell death before degranulation, so that embryos fail to hatch. Chimera analyses show that Spint2 is required in hatching gland cells, but not in the overlying periderm, their potential migration and adhesion substrate. Spint2 acts independently of all tested Matriptases, Prostasins and other described Spint1 and Spint2 mediators. However, it displays a tight genetic interaction with and acts at least partly via the cell-cell adhesion protein E-cadherin, promoting both hatching gland cell cohesiveness and survival, in line with formerly reported effects of E-cadherin during morphogenesis and cell death suppression. In contrast, no such genetic interaction was observed between Spint2 and the cell-cell adhesion molecule EpCAM, which instead interacts with Spint1a. Our data shed new light onto the mechanisms of hatching gland morphogenesis and hatching gland cell survival. In addition, they reveal developmental roles of Spint2 that are strikingly different from those of Spint1, most likely due to differences in the expression patterns and relevant target proteins.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping