Annals of Anatomy 194 (2012) 334–338
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Annals of Anatomy
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Research article
Expression analysis of ADAM17 during mouse eye development
Saadettin Sel
a,∗,1
, Thomas Kalinski
b,1
, Isabelle Enssen
a
, Maja Kaiser
a
, Norbert Nass
a
,
Stefanie Trau
a
, Gregor Wollensak
a
, Lars Bräuer
c,d
, Kristin Jäger
c
, Friedrich Paulsen
c,d
a
Department of Ophthalmology (Experimental Ophthalmology), Martin Luther University Halle/Wittenberg, Erst-Grube-Str. 40, D-06120 Halle/Saale, Germany
b
Department of Pathology, Otto-von-Guericke-University, Magdeburg, Germany
c
Department of Anatomy and Cell Biology, Martin Luther University Halle/Wittenberg, Halle/Saale, Germany
d
Department of Anatomy II, University of Erlangen-Nuremberg, Erlangen, Germany
a r t i c l e i n f o
Article history:
Received 5 July 2011
Received in revised form
26 September 2011
Accepted 7 October 2011
Keywords:
ADAM17
Gene expression
Embryo
Eye development
Corneal epithelium
Ciliary body epithelial cells
Retinal vessels
s u m m a r y
ADAM17 (a disintegrin and metallopeptidase domain 17) is crucial for eye morphogenesis. In this study
we analysed the expression pattern of ADAM17 during mouse eye development.
ADAM17 expression in adult retina was examined using the reverse transcription-polymerase chain
reaction (RT-PCR) and verification of the RT-PCR products by DNA sequencing. Immunohistochemistry
was performed to evaluate the ADAM17 expression pattern in mouse eyes at developmental stages of
embryonic day (E) 12, E14, E16, E18, postnatal day (P) 0, P1, P4, P7, P14, P 30 and P175 (adult).
We detected ADAM17 mRNA in adult retina tissue. ADAM17 protein was expressed in non-pigmented
ciliary epithelial cells and in retinal vessels from P7 onwards during eye development. In corneal epithelial
cells and endothelium, ADAM17 protein was present from P14 onwards.
Although, mice in which the functional ADAM17 gene is significantly reduced develop multiple eye
malformations, the expression of ADAM17 is not ubiquitous over the entire eye. Its expression pattern
during development suggests that not only TNF-alpha but additional membrane-anchored substrates of
ADAM17 play an important role in eye formation.
© 2011 Elsevier GmbH. All rights reserved.
1. Introduction
During embryogenesis, the mammalian eye develops from all
three blastodermic layers. The retina and retinal pigment epithe-
lium (RPE) develop from the neuroectoderm whereas cornea and
sclera arise mainly from the mesoderm and the lens is derived from
the surface ectoderm (Graw, 2010; Kondoh, 2002).
In humans, corneal epithelium consists of 5–7 cell layers which
are regenerated continuously or after injury by limbal stem cells.
Under physiological conditions, a complete turnover time of the
corneal epithelium is about 7 days. During this renewal pro-
cess, limbal stem cells develop a single layer of columnar basal
cells resting on the basement membrane. The basal cells can
proliferate and differentiate to suprabasal or wing cells. Finally,
the wing cells evolve into 1–3 layers of superficial squamous
cells. In particular, the basal cells of the corneal epithelium have
This work was supported in part by the Deutsche Forschungsgemeinschaft (SE
1995/1-1) and the Wilhelm-Roux program (FKZ 10/41) from Martin Luther Univer-
sity Halle-Wittenberg.
∗
Corresponding author. Tel.: +49 345 557 1878; fax: +49 345 557 1848.
E-mail address: saadettinsel@googlemail.com (S. Sel).
URL: http://www.medizin.uni-halle.de/kau/index.php?cid=1123 (S. Sel).
1
Both authors contributed equally to this work.
several important functions. Besides generating new wing cells,
basal cells secrete extracellular matrix molecules that form the
basement membrane and are involved in the organization of the
hemidesmosomes to stabilize the connection to the underlying
basement membrane. Abnormalities in this attachment result clin-
ically in recurrent corneal erosion syndromes or in persistent
corneal epithelial defects (Pajoohesh-Ganji and Stepp, 2005).
The ciliary epithelium consists of an outer pigmented ciliary
epithelium facing the stroma of the ciliary body and an inner
non-pigmented ciliary epithelium facing the vitreous cavity. By an
active ion transport mechanism, ciliary epithelium is responsible
for aqueous humor production that is crucial for the maintenance
of a constant intraocular pressure. Dysregulation of the intraocular
pressure leads to debilitating visual impairment (Delamere, 2005).
The retinal blood vessels are highly organized to supply the
retina with sufficient blood with minimal interference of the light
path to the photoreceptors. During embryogenesis, the retinal vas-
culature develops radially from the optic nerve head towards the
periphery at the ganglion cell layer (GCL) forming the superficial
vascular plexus. The superficial vessels branch into inner layers
of the retina and form the deep vascular plexus along the outer
edge of the inner nuclear layer (INL), and the intermediate vascu-
lar plexus along the inner edge of the INL (Bromberg-White et al.,
2009; Dorrell et al., 2007).
0940-9602/$ – see front matter © 2011 Elsevier GmbH. All rights reserved.
doi:10.1016/j.aanat.2011.10.008