Publication:
Ciliary muscle in avian is derived from mesenchymal and epithelial cells

Loading...
Thumbnail Image
Full text at PDC
Publication Date
2002-06
Authors
Barrio Asensio, María del Carmen
Puerta Fonollá, Javier
Advisors (or tutors)
Editors
Journal Title
Journal ISSN
Volume Title
Publisher
Elsevier
Citations
Google Scholar
Research Projects
Organizational Units
Journal Issue
Abstract
It has long been maintained that the ciliary muscle derives from mesenchymal cells. The embryonic development of the avian ciliary muscle was studied in chick embryos from stage 25 HH to the time of hatching. Serial sections of the eye were stained routinely or immunocytochemically using the monoclonal antibody 13F4, which recognizes a cytoplasmic antigen specific for all types of muscle cells. We found that the mesenchymal immunoreactive cells, at stage 37 HH, are arranged in two distinct orientations forming the anterior and posterior portions of the ciliary muscle. At stages 38 and 39 HH the pigmented epithelium contained 13F4 positive cells, which detach from the epithelium and apparently migrate into stroma. These epithelial cells may differentiate into muscle cells. Within this same time period a progressive accumulation of myoblasts was detected between the pigmented epithelium and the ciliary muscle. Some myoblasts containing melanin were also observed. At stage 40 HH the internal portion of the ciliary muscle was visible. These findings indicate that the immunopositive epithelial cells participate in the formation of the internal portion of the muscle. We conclude that the ciliary muscle derives not only from the mesenchymal cells but also from the pigmented epithelium.
Description
Received 28 December 2001, Revised 7 February 2002, Available online 28 May 2002
Keywords
Citation
1- Bard, J. B., & Ross, A. S. (1982a). The morphogenesis of the ciliary body of the avian eye. I. Lateral cell detachment facilitates epithelial folding. Developmental Biology, 92, 73–86. 2- Bard, J. B., & Ross, A. S. (1982b). The morphogenesis of the ciliary body of the avian eye. II. Differential enlargement causes an epithelium to form radial folds. Developmental Biology, 92, 87–96. 3- Barrio-Asensio, C., Murillo-Gonz�alez, J., Peña-Meli�an, A., & Puerta-Fonoll�a, J. (1999). Immunocytochemical study on the triple origin of the sphincter iris in the chick embryo. Development, Genes and Evolution, 209, 620–624. 4- Coulombre, A. J., & Coulombre, J. L. (1957). The role of intraocular pressure in the development of the chick eye. III. Ciliary body. The American Journal of Ophthalmology, 44, 85–92. 5- Gabella, G., & Clarke, E. (1983). Embryonic development of the smooth and striated musculatures of the chicken iris. Cell and Tissue Research, 229, 37–59. 6- Geberg, A. (1884). Uber die nerven der Iris und des Ciliarkorpers bei Vogeln. Internationale Monatsschrift f€ur Anatomie und Histologie, 1, 7–52. 7- Hamburger, V., & Hamilton, H. L. (1951). A series of normal stages in the development of the chick embryo. Journal of Morphology, 88, 49–92. 8- Johnston, M. C., Noden, D. M., Hazelton, R. D., Coulombre, J. L., & Coulombre, A. J. (1979). Origins of avian ocular and periocular tissues. Experimental Eye Research, 29, 27–43. 9- Lai, Y. L. (1972a). The development of the sphincter muscle in the iris of the albino rat. Experimental Eye Research, 14, 196–202. 10- Lai, Y. L. (1972b). The development of the dilator muscle in the iris of the albino rat. Experimental Eye Research, 14, 203–207. 11- Leplat, G. (1912). Recherches sur le d�eveloppement et la structure de la membrane vasculaire de l’oeil des oiseaux. Archives de Biologie (Li�ege), 27, 403–523. 12- Lewis, W. H. (1903). Wandering pigmented cells arising from the epithelium of the optic cup, with observations on the origin of the m. sphincter pupillae in the chick. The American Journal of Anatomy, 2, 405–416. 13- Link, B. A., & Nishi, R. (1998a). Development of the avian iris and ciliary body: the role of activin and follistatin in coordination of the smooth-to-striated muscle transition. Developmental Biology, 199, 226–234. 14- Link, B. A., & Nishi, R. (1998b). Development of the avian iris and ciliary body: mechanisms of cellular differentiation during the smooth-to-striated muscle transition. Developmental Biology, 203, 163–176. 15- Lucchi, M. L., Bortolami, R., & Callegari, E. (1974). Fine structure of intrinsic eye muscle of birds: development and postnatal changes. Journal of Submicroscopic Cytology, 6, 205–218. 16- Murphy, Ch. J., Glasser, A., & Howland, H. C. (1995). The anatomy of the ciliary region of the chicken eye. Investigative Ophthalmology and Visual Science, 36, 889–890. 17- Pardue, M. T., & Sivak, J. G. (1997). The functional anatomy of the ciliary muscle in four avian species. Brain Behavior and Evolution, 49, 295–311. 18- Peirone, S., Sisto-Daneo, L., & Filogamo, G. (1990). Embryogenesis of the avian iris sphincter muscle: in vivo and in vitro studies. International Journal of Developmental Neuroscience, 8, 17–31. 19- Reichman, E. F., & Beebe, D. C. (1990). Acetylcholinesterase activity as a marker for the development of the ciliary epithelium in the chicken embryo. Experimental Eye Research, 51, 249–255. 20- Rong, P. M., Ziller, C., Pe~na-Meli�an, A., & Le Douarin, N. (1987). A monoclonal antibody specific for avian early myogenic cells and differentiated muscle. Developmental Biology, 122, 338–353. 21- Scapolo, P. A., Peirone, S. M., Filogamo, G., & Veggetti, A. (1988). Histochemical, immunohistochemical, and ultrastructural observations on the iris muscles of Gallus gallus. The Anatomical Record, 221, 687–699. 22- Yamashita, T., & Sohal, G. S. (1986). Development of smooth and skeletal muscle cells in the iris of the domestic duck, chick and quail. Cell and Tissue Research, 244, 121–131.
Collections