TY - JOUR
T1 - Distribution of N-cadherin in human cerebral cortex during prenatal development
AU - Tanriover, Gamze
AU - Kayisli, Umit A.
AU - Demir, Ramazan
AU - Pestereli, Elif
AU - Karaveli, Seyda
AU - Demir, Necdet
N1 - Funding Information:
Fig. 7a–d Representative serial sections for N-cadherin and Tuj-1 stainings from developing cerebral neocortex during second trimester. Similar immunoreactivities are seen for both proteins in a cell type manner (compare group II a–d with group III a–d). Group I a–d Negative staining for N-cadherin and stained with hematoxylin. Group II a–d N-cadherin immunoreactivity from different neocortex layers. Group III a–d Tuj-1 immunoreactivity from different neocortex layers that matched to group II pairs. Group IV a, b Negative staining for Tuj-1 (human decidua). Group IV c, d A negative tissue for Tuj-1 staining. Group I a–d ×40; groups II–IV a–d ×20 Acknowledgements This study is a part of the master thesis of Gamze Tanriover and is partially supported by the Research Fund of Akdeniz University, Antalya, Turkey. The authors would like to thank Prof. Dr. Joel C. Glover for helpful discussions and advice and for critically editing the manuscript.
Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2004/9
Y1 - 2004/9
N2 - An important subgroup of adhesion molecules is the superfamily of cadherins, which takes part in cell recognition and differentiation during development. To our knowledge only one study describing N-cadherin expression in developing human brain has been performed so far. Our aim is to identify N-cadherin expression to establish a relationship between its expression and function in human cerebral cortex during prenatal development. In the present study, localization and intensity of N-cadherin was investigated in developing cerebral cortex. Fetuses from spontaneous abortions (n=13) were obtained from first, second, and third trimesters. Western blot analysis revealed three bands and the third trimester samples showed the strongest bands for N-cadherin. Cell processes, axon bundles, and some of the developing neurons revealed immunoreactivity for N-cadherin throughout pregnancy. The immunoreactivity increased in the developing neocortex and expanded from the ventricular layer toward the marginal zone as development progressed. Moreover, the immunoreactivity was strong in vascular endothelium during all three trimesters. We conclude that N-cadherin is dynamically related to the organization of cerebral cortex layers during prenatal development. The dynamic expression pattern implicates N-cadherin as a potential regulator of cell migration, axon extension and fasciculation, the establishment of synaptic contacts, and neurovascular angiogenesis in the developing human cerebral cortex.
AB - An important subgroup of adhesion molecules is the superfamily of cadherins, which takes part in cell recognition and differentiation during development. To our knowledge only one study describing N-cadherin expression in developing human brain has been performed so far. Our aim is to identify N-cadherin expression to establish a relationship between its expression and function in human cerebral cortex during prenatal development. In the present study, localization and intensity of N-cadherin was investigated in developing cerebral cortex. Fetuses from spontaneous abortions (n=13) were obtained from first, second, and third trimesters. Western blot analysis revealed three bands and the third trimester samples showed the strongest bands for N-cadherin. Cell processes, axon bundles, and some of the developing neurons revealed immunoreactivity for N-cadherin throughout pregnancy. The immunoreactivity increased in the developing neocortex and expanded from the ventricular layer toward the marginal zone as development progressed. Moreover, the immunoreactivity was strong in vascular endothelium during all three trimesters. We conclude that N-cadherin is dynamically related to the organization of cerebral cortex layers during prenatal development. The dynamic expression pattern implicates N-cadherin as a potential regulator of cell migration, axon extension and fasciculation, the establishment of synaptic contacts, and neurovascular angiogenesis in the developing human cerebral cortex.
KW - Cerebral cortex
KW - Developing brain
KW - Human fetus
KW - N-cadherin
KW - Prenatal period
UR - https://www.scopus.com/pages/publications/5644244405
U2 - 10.1007/s00418-004-0691-z
DO - 10.1007/s00418-004-0691-z
M3 - Article
C2 - 15309553
AN - SCOPUS:5644244405
SN - 0948-6143
VL - 122
SP - 191
EP - 200
JO - Histochemistry and Cell Biology
JF - Histochemistry and Cell Biology
IS - 3
ER -