JDR JDR Most Cited Articles
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Abstract Freely available
Right arrow Full Text
Right arrow Full Text (PDF)
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via ISI Web of Science (3)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Nagata, J.
Right arrow Articles by Yamane, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nagata, J.
Right arrow Articles by Yamane, A.

Progress of Cell Proliferation in Striated Muscle Tissues during Development of the Mouse Tongue

J. Nagata, and A. Yamane*

Department of Pharmacology, Tsurumi University School of Dental Medicine, 2-1-3 Tsurumi, Tsurumi-ku, Yokohama 230-8501, Japan;



View larger version (13K):

[in a new window]
 
Figure 1. Electrophoretic gel pattern (A) of cyclin D1 cDNA standard and its competitor after competitive PCR, and the standard curve (B). Chronological changes in the expression level of cyclin D1 mRNA in mouse tongues at embryonic days (E) 11, 13, 15, 17, and birth as analyzed by competitive RT-PCR (C). Each point with its vertical bar represents the mean ± 1 SD of 5 samples. The vertical axis is expressed as a percentage of the mean value at E11.

 


View larger version (154K):

[in a new window]
 
Figure 2. Immunostaining images for PCNA (A-C) and desmin (D) in the somites 2, 3 (A), 4, 5 (B), and 3 (C,D) of the E9 mouse embryo. The diagrammatic representations show sagittal sections of tongues at E11 (E) and E13 ~ birth (F), viewed from the buccal side. The dotted rectangles indicate the regions in which proliferating cell nuclear antigen (PCNA)-labeling indices were obtained. Immunostaining images for PCNA (G,H,K-N) and fast myosin heavy-chain (I,O-R) in the whole portion of the E11 tongue (G,I), and in the anterior (K,L,O,P), middle (M,Q), and posterior (N,R) regions of E13 tongues. A control staining image of a whole portion of an E11 tongue treated with normal mouse IgG instead of the antibodies (J). H, L, and P are higher-magnification images of the regions indicated by the rectangles in G, K, and O, respectively. White lines in L contour the areas which lack the PCNA-positive cell nuclei.

 


View larger version (123K):

[in a new window]
 
Figure 3. Immunostaining images for PCNA (A-H) and fMHC (I-L) in the anterior (A,E,I), middle (B,F,J), and posterior (C,D,G,H,K,L) regions of E15 (A-D) and E17 (E-L) tongues. Chronological changes in the PCNA-labeling index in mouse tongues between E11 and birth (M). D, H, and L are higher-magnification images of the regions indicated by the rectangles in C, G, and K, respectively.

 


View larger version (12K):

[in a new window]
 
Figure 4. The stages in which commitment, migration, proliferation, differentiation, and maturation occur most actively during the development of the mouse tongue. Data for the commitment, migration, differentiation, and maturation stages are from the results of Mayo et al.(1992), Yamane et al.(2000), and Amano et al.(2002).

 





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
IADR Journals Advances in Dental Research ®
Journal of Dental Research ® Critical Reviews (1990-2004)
Copyright © 2004 Institutional Access Guidelines