|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Development, Vol 112, Issue 2 627-637, Copyright © 1991 by Company of Biologists
JOURNAL ARTICLES |
B Wehrle-Haller, M Koch, S Baumgartner, J Spring and M Chiquet
Department of Biophysical Chemistry, Biocenter of the University, Basel, Switzerland.
The extracellular matrix protein, tenascin, appears in a restricted pattern during organ morphogenesis. Tenascin accumulates along developing peripheral nerves as they leave the spinal cord and enter the limb mesenchyme (Wehrle and Chiquet, Development 110, 401-415, 1990). Here we found that most but not all tenascin deposited along growing nerves is of glial origin. By in situ hybridization with a tenascin cDNA probe, we determined the site of tenascin mRNA accumulation both in normal and nerve-free limbs. In normal wing buds, tenascin mRNA was first detected within the developing limb nerves. Vinculin-positive glial precursor cells, which comigrate with the axons, are the likely source of this tenascin message. In nerveless wing grafts, tenascin was first expressed in tendon primordia in the absence, and thus independently, from innervation. In contrast to normal limbs, grafted wing buds neither contained vinculin-positive glial precursor cells, nor expressed tenascin in regions proximal to tendon primordia. In normal wing buds, tenascin deposited by tendon primordia transiently parallels and surrounds certain developing nerves. After the major nerve pattern is established, tenascin mRNA disappears from nerves in the upper limb, but is expressed in perichondrium and tendons. We propose that glial tenascin facilitates the penetration of axons into the limb bud and is important for nerve fasciculation. In some places, early tendon primordia might help to guide the migration of axons and glial precursor cells towards their target.
This article has been cited by other articles:
![]() |
T. Sugawara, B.T. Himes, M. Kowada, M. Murray, A. Tessler, and W. P. Battisti Putative Inhibitory Extracellular Matrix Molecules Do Not Prevent Dorsal Root Regeneration into Fetal Spinal Cord Transplants Neurorehabil Neural Repair, June 1, 1999; 13(2): 135 - 147. [Abstract] [PDF] |
||||
![]() |
L. M. Moscoso, H. Cremer, and J. R. Sanes Organization and Reorganization of Neuromuscular Junctions in Mice Lacking Neural Cell Adhesion Molecule, Tenascin-C, or Fibroblast Growth Factor-5 J. Neurosci., February 15, 1998; 18(4): 1465 - 1477. [Abstract] [Full Text] [PDF] |
||||
![]() |
G Kardon Muscle and tendon morphogenesis in the avian hind limb Development, January 10, 1998; 125(20): 4019 - 4032. [Abstract] [PDF] |
||||
![]() |
R. Tucker, J. Hammarback, D. Jenrath, E. Mackie, and Y Xu Tenascin expression in the mouse: in situ localization and induction in vitro by bFGF J. Cell Sci., January 1, 1993; 104(1): 69 - 76. [Abstract] [PDF] |
||||
![]() |
R. Tucker The in situ localization of tenascin splice variants and thrombospondin 2 mRNA in the avian embryo Development, January 1, 1993; 117(1): 347 - 358. [Abstract] [PDF] |
||||
![]() |
M Umbhauer, J. Riou, J Spring, J. Smith, and J. Boucaut Expression of tenascin mRNA in mesoderm during Xenopus laevis embryogenesis: the potential role of mesoderm patterning in tenascin regionalization Development, January 9, 1992; 116(1): 147 - 157. [Abstract] [PDF] |
||||