TY - JOUR
T1 - High-resolution episcopic microscopy
T2 - A rapid technique for high detailed 3D analysis of gene activity in the context of tissue architecture and morphology
AU - Weninger, Wolfgang J.
AU - Geyer, Stefan H.
AU - Mohun, Timothy J.
AU - Rasskin-Gutman, Diego
AU - Matsui, Takaaki
AU - Ribeiro, Ines
AU - Costa, Luciano Da F.
AU - Izpisúa-Belmonte, Juan Carlos
AU - Müller, Gerd B.
PY - 2006/6
Y1 - 2006/6
N2 - We describe a new methodology for rapid 2D and 3D computer analysis and visualisation of gene expression and gene product pattern in the context of anatomy and tissue architecture. It is based on episcopic imaging of embryos and tissue samples, as they are physically sectioned, thereby producing inherently aligned digital image series and volume data sets, which immediately permit the generation of 3D computer representations. The technique uses resin as embedding medium, eosin for unspecific tissue staining, and colour reactions (β-galactosidase/Xgal or BCIP/NBT) for specific labelling of gene activity and mRNA pattern. We tested the potential of the method for producing high-resolution volume data sets of adult human and porcine tissue samples and of specifically and unspecifically stained mouse, chick, quail, frog, and zebrafish embryos. The quality of the episcopic images resembles the quality of digital images of true histological sections with respect to resolution and contrast. Specifically labelled structures can be extracted using simple thresholding algorithms. Thus, the method is capable of quickly and precisely detecting molecular signals simultaneously with anatomical details and tissue architecture. It has no tissue restrictions and can be applied for analysis of human tissue samples as well as for analysis of all developmental stages of embryos of a wide variety of biomedically relevant species.
AB - We describe a new methodology for rapid 2D and 3D computer analysis and visualisation of gene expression and gene product pattern in the context of anatomy and tissue architecture. It is based on episcopic imaging of embryos and tissue samples, as they are physically sectioned, thereby producing inherently aligned digital image series and volume data sets, which immediately permit the generation of 3D computer representations. The technique uses resin as embedding medium, eosin for unspecific tissue staining, and colour reactions (β-galactosidase/Xgal or BCIP/NBT) for specific labelling of gene activity and mRNA pattern. We tested the potential of the method for producing high-resolution volume data sets of adult human and porcine tissue samples and of specifically and unspecifically stained mouse, chick, quail, frog, and zebrafish embryos. The quality of the episcopic images resembles the quality of digital images of true histological sections with respect to resolution and contrast. Specifically labelled structures can be extracted using simple thresholding algorithms. Thus, the method is capable of quickly and precisely detecting molecular signals simultaneously with anatomical details and tissue architecture. It has no tissue restrictions and can be applied for analysis of human tissue samples as well as for analysis of all developmental stages of embryos of a wide variety of biomedically relevant species.
KW - 3D reconstruction
KW - Anatomy
KW - Embryology
KW - Gene expression analysis
KW - RNA pattern
UR - http://www.scopus.com/inward/record.url?scp=33646868163&partnerID=8YFLogxK
U2 - 10.1007/s00429-005-0073-x
DO - 10.1007/s00429-005-0073-x
M3 - Article
C2 - 16429276
AN - SCOPUS:33646868163
SN - 0340-2061
VL - 211
SP - 213
EP - 221
JO - Anatomy and Embryology
JF - Anatomy and Embryology
IS - 3
ER -