Accumulation of collagen III at the cleft points of developing mouse submandibular epithelium.

The distribution of collagens I, III, IV and V was studied by immunoperoxidase staining of early developing mouse submandibular glands. Collagen I was always present in the extracellular matrices of the mesenchyme and at the epithelial-mesenchymal interfaces of the 12-day gland with no clefts and of the 13-day gland with a few definite clefts. Collagen III was found in a similar fashion to that of collagen I in the mesenchyme, but the distribution at the epithelial-mesenchymal interfaces was very different. In the mid 12-day gland with a round lobule, collagen III was distributed at every slightly indented site of basal epithelial surfaces. At the late 12-day stage, a few initial signs of cleft appeared on the surface, at which accumulation of collagen III became evident. Intense immunoreaction of collagen III in the early 13-day gland was seen at the bottom of every narrow cleft. No specific accumulation of collagens IV and V was observed in clefts of the late 12-day and early 13-day glands. Staining of collagen III in the 12-day gland cultured for 10 h in the presence of bovine dental pulp collagenase inhibitor, which has been shown to stimulate cleft initiation, was very prominent at the bottom of every narrow cleft. These observations suggest that collagen III works as a key substance for either in vitro or in vivo cleft initiation of the mouse embryonic submandibular epithelium.

[1]  C. Grobstein,et al.  Collagenase: effect on the morphogenesis of embryonic salivary epithelium in vitro. , 1965, Science.

[2]  Y. Fukuda,et al.  The role of interstitial collagens in cleft formation of mouse embryonic submandibular gland during initial branching. , 1988, Development.

[3]  B. Sykes,et al.  The estimation of two collagens from human dermis by interrupted gel electrophoresis. , 1976, Biochemical and biophysical research communications.

[4]  N. K. Wessells,et al.  Effects of collagenase on developing epithelia in vitro: lung, ureteric bud, and pancreas. , 1968, Developmental biology.

[5]  N. K. Wessells,et al.  Intra- and extracellular control of epithelial morphogenesis. , 1970, The ... Symposium. Society for Developmental Biology. Symposium.

[6]  J. Kishi,et al.  Collagenase inhibitor stimulates cleft formation during early morphogenesis of mouse salivary gland. , 1986, Developmental biology.

[7]  B. Spooner,et al.  Collagen involvement in branching morphogenesis of embryonic lung and salivary gland. , 1980, Developmental biology.

[8]  T. Hayakawa,et al.  Isolation and characterization of type V collagen from human post-burn granulation tissues. , 1986, The Journal of investigative dermatology.

[9]  J. Kishi,et al.  Scanning electron microscopic observation of mouse embryonic submandibular glands during initial branching: preferential localization of fibrillar structures at the mesenchymal ridges participating in cleft formation. , 1986, Journal of embryology and experimental morphology.

[10]  J. Paranko Expression of type I and III collagen during morphogenesis of fetal rat testis and ovary , 1987, The Anatomical record.

[11]  J. Kishi,et al.  Local effects of implanted Elvax chips containing collagenase inhibitor and bacterial collagenase on branching morphogenesis of mouse embryonic submandibular glands in vitro , 1986 .

[12]  M. W. Jennison Bacterial Collagenase , 1945, Journal of bacteriology.

[13]  M. Bernfield,et al.  DEPENDENCE OF SALIVARY EPITHELIAL MORPHOLOGY AND BRANCHING MORPHOGENESIS UPON ACID MUCOPOLYSACCHARIDE-PROTEIN (PROTEOGLYCAN) AT THE EPITHELIAL SURFACE , 1972, The Journal of cell biology.

[14]  M. Karnovsky,et al.  THF EARLY STAGES OF ABSORPTION OF INJECTED HORSERADISH PEROXIDASE IN THE PROXIMAL TUBULES OF MOUSE KIDNEY: ULTRASTRUCTURAL CYTOCHEMISTRY BY A NEW TECHNIQUE , 1966, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[15]  T. Mizuno,et al.  Mesenchymal control over elongating and branching morphogenesis in salivary gland development. , 1981, Journal of embryology and experimental morphology.

[16]  J. Thiery,et al.  Distribution of laminin and collagens during avian neural crest development. , 1987, Development.

[17]  H. Nogawa Determination of the curvature of epithelial cell mass by mesenchyme in branching morphogenesis of mouse salivary gland. , 1983, Journal of embryology and experimental morphology.

[18]  Y Nakanishi,et al.  Cell proliferation is not required for the initiation of early cleft formation in mouse embryonic submandibular epithelium in vitro. , 1987, Development.

[19]  M. Bernfield,et al.  Heparan sulfate proteoglycans from mouse mammary epithelial cells. Cell surface proteoglycan as a receptor for interstitial collagens. , 1985, The Journal of biological chemistry.

[20]  T. Yamagata,et al.  Purification and properties of bacterial chondroitinases and chondrosulfatases. , 1968, The Journal of biological chemistry.

[21]  C. Little,et al.  Cellular events associated with lung branching morphogenesis including the deposition of collagen type IV. , 1987, Developmental biology.

[22]  J. Kishi,et al.  Purification and characterization of bovine dental pulp collagenase inhibitor. , 1984, Journal of biochemistry.

[23]  R. Jaenisch,et al.  Normal epithelial branching morphogenesis in the absence of collagen I. , 1986, Developmental biology.

[24]  Y. Nakanishi,et al.  Mechanical aspects of the mesenchymal influence on epithelial branching morphogenesis of mouse salivary gland , 1987 .

[25]  R. Jaenisch,et al.  Collagen synthesis by cell lines derived from Mov-13 mouse embryos which have a lethal mutation in the collagen alpha 1(I) gene. , 1987, The Biochemical journal.

[26]  R. Glanville,et al.  Isolation and Characterization of a Native Placental Basement-Membrane Collagen and Its Component α Chains , 1979 .

[27]  R. Timpl,et al.  The genetically distinct collagens , 1985 .

[28]  K. Kratochwil Organ specificity in mesenchymal induction demonstrated in the embryonic development of the mammary gland of the mouse. , 1969, Developmental biology.