spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by HALE, L. J.
Right arrow Search for Related Content
PubMed
Right arrow Articles by HALE, L. J.

Quarterly Journal of Microscopical Science, Vol s3-97, 355-368, Copyright © 1956 by Company of Biologists

Mesodermal Cell Deaths during the Early Development of the Scleral Bones in the Chick

L. J. HALE 1

1 Department of Zoology, West Mains Road, Edinburgh 9

1. The positions of degenerating cells in the mesenchyme of the scleral bone primordia of the chick, and in the fibrous sclera beneath them, have been ascertained.

2. It is shown that the number of cell deaths within the bone primordia, and also beneath them in the fibrous sclera, is markedly higher than, and follows a different pattern from the regions between.

3. A centre of cell destruction is seen to occur at and near to the boundary of the mesenchyme and fibrous sclera. This begins in 7- to 8-day primordia, rises to a peak at 8 to 9 days, and subsides in 9- to 10-day primordia.

4. A second centre of cell death occurs in the mesenchyme nearer to the conjunctival papilla. It starts in 8- to 9-day eyes about mid-way between the conjunctiva and sclera, and as it increases in intensity, the centre moves nearer to the conjunctival papilla (9 to 10 days), beneath which it appears to subside (some 10-day primordia).

5. The function of these waves of cell destruction is discussed. It is concluded that their most likely function is morphogenetic; they may make a space into which the osteogenic cells migrate, or they may ensure a normal position and shape for the developing bone. Consideration has also been given to the possibility that the products of cell death might have a histiogenetic function.







© The Company of Biologists Ltd 1956