Effect of ascorbic acid deficiency on mouse second molar tooth germs cultivated in vitro

Development ◽  
1976 ◽  
Vol 36 (1) ◽  
pp. 73-85
Author(s):  
Gordon E. Levenson

Mandibular second molar tooth germs from two-day old mice were cultured in vitro, on millipore membranes, for periods of up to 20 days in liquid medium with or without added ascorbic acid. Tooth germs grown in ascorbate medium were characterized by relatively normal growth, differentiation, morphology and histology. Cuspation patterns were maintained. The epithelial root sheath continued to grow along the millipore membrane. Tooth germs cultured in ascorbate-deficient medium manifested a consistent and striking failure in maintenance of differentiated odontoblastic and ameloblastic tissue with arrest of predentin synthesis, severe structural collapse and reduction in size. Cuspation patterns were lost in scorbutic molars, with sinking of surface layers into pulpal tissue and flattening of the entire organ. This resulted in a lack of recognizable morphology and in severe disorganization of tissues. Only growing areas of the root sheath with associated proliferation of preameloblasts and pre-odontoblasts and adjacent pulpal tissue remained normal and refractory to ascorbate deficiency. Odontoblastic as well as ameloblastic layers were disrupted and cells were dedifferentiated. Newly differentiated odontoblasts became highly vacuolated when they became polarized and started to secrete extracellular matrix.

Development ◽  
1977 ◽  
Vol 37 (1) ◽  
pp. 49-57
Author(s):  
John R. Schiltz ◽  
Joel Rosenbloom ◽  
Gordon E. Levenson

Second molar tooth germs from 2-day-old Swiss-Webster mice, grown in organ culture for 7 days in ascorbic-acid-deficient medium, synthesized about 65 % as much protein (measured by incorporation of [14C]proline during a 24-h pulse) as did ascorbic-acid-supplemented controls. The newly synthesized proteins from ascorbic-acid-deficient cultures contained only about 7% of the hydroxyproline content of the controls. Collagenase digestion of the newly synthesized proteins showed that collagen comprised the same fraction of the total protein synthesized under both culture conditions. This result indicates that the ascorbatedeficient cultures made significant quantities of underhydroxylated collagen. Partial characterization of the collagen alpha chains on carboxymethyl cellulose columns showed an α1/α2 ratio of about 5, suggesting that at least two different species of collagen were synthesized. The α1/α2 ratio of the chains recovered from the ascorbate-deficient cultures was also about 5 but the chains were slightly underhydroxylated and the total amount of these chains which could be identified accounted for only a small fraction of the total collagen which was synthesized. A large fraction of the synthesized collagenous protein was found in the culture medium, mostly in the form of lower molecular weight peptides. It is concluded that most of the collagen which is synthesized by ascorbate-deficient tooth-bud cultures is not utilized by the component tissues, but is probably degraded and released into the medium.


1986 ◽  
Vol 246 (3) ◽  
pp. 623-634 ◽  
Author(s):  
I. Gorter de Vries ◽  
P. C. Ameloot ◽  
D. Coomans ◽  
E. Wisse

2007 ◽  
Vol 86 (11) ◽  
pp. 1063-1067 ◽  
Author(s):  
M. Tummers ◽  
T. Yamashiro ◽  
I. Thesleff

Mouse molars are normally not capable of continuous growth. We hypothesized that the mouse molar has intrinsic potential to maintain the epithelial stem cell niche and assessed this potential by growth in vitro. Although the tooth germs flattened considerably, they developed a mineralized crown and a root. However, histologically, the root surface was composed of 3 structurally different regions affecting the fate of the dental epithelium. The anterior and posterior aspects maintained the morphological and molecular characteristics of the cervical loop of a continuously growing incisor, with a continuous layer of ameloblasts. The epithelium making contact with the supporting filter resembled Hertwig’ss epithelial root sheath. The top of the cultured molar exposed to air lacked epithelium altogether. We conclude that the fate of the epithelium is regulated by external cues influenced by culture conditions, and that the molar has the intrinsic capacity to grow continuously.


1997 ◽  
Vol 105 (1) ◽  
pp. 52-58 ◽  
Author(s):  
D. M. Lyaruu ◽  
M. A. Duin ◽  
T. J. M. Bervoets ◽  
J. H. M. Wöltgens ◽  
A. L. J. J. Bronckers

1998 ◽  
Vol 106 (S1) ◽  
pp. 156-159 ◽  
Author(s):  
Joseph H. M. Wöltgens ◽  
Donacian M. Lyaruu ◽  
Antonius L. J. J. Bronckers ◽  
Marion A. Duin ◽  
Theodor J. M. Bervoets

1988 ◽  
Vol 14 (5) ◽  
pp. 207-213 ◽  
Author(s):  
Franklin S. Weine ◽  
Richard A. Pasiewicz ◽  
R. Ted Rice

Endodontology ◽  
2017 ◽  
Vol 29 (2) ◽  
pp. 90
Author(s):  
Ruchi RaniPurvesh Shah ◽  
TapatiManohar Sinhal ◽  
NimishaChinmay Shah ◽  
PratikSubhas Jais ◽  
KrupaliDhirubhai Hadwani

1987 ◽  
Vol 1 (2) ◽  
pp. 196-201 ◽  
Author(s):  
J.H.M. Woltgens ◽  
D.M. Lyaruu ◽  
TH.J.M. Bervoets ◽  
A.L.J.J. Bronckers

We examined the effects of various calcium (Ca) and phosphate (P) levels on enamel matrix synthesis, secretion, and its subsequent mineralization in vitro. Second maxillary molar tooth germs of three-day-old hamsters were cultured for nine days in vitro in media containing low (0.9 mmol/L), moderate (2.6 mmol/L), or high (4.5 mmol/L) medium levels of Ca, with either moderate (1.65 mmol/L) or high (3.65 mmol/ L) medium levels of P. Explants were then examined histologically. For examination of matrix synthesis and mineralization, explants were labeled during the last 24 hr of culture with a triple label of 3H-proline, 45Ca, and 32PO4. At low Ca levels, tooth germs failed to deposit enamel matrix and dentin, and no mineralization took place, regardless of the levels of P. Low levels of Ca, however, did not prevent deposition of pre-dentin. At moderate and high levels of Ca, considerable amounts of enamel and dentin were deposited in vitro, and both matrices mineralized. At high Ca levels, however, the forming enamel hypermineralized, was more irregular, and tended to be thinner. Increasing P concentrations at moderate and high Ca levels resulted in formation of a more regular enamel and dentin and a better-controlled mineralization. Biochemically, high levels of Ca tended to decrease enamel matrix secretion but significantly enhanced the uptake of 45Ca. This Ca-stimulated increase of 45Ca uptake could be reduced to below control levels by increases in P medium levels. We conclude that: (1) a minimum medium Ca concentration is required to induce enamel matrix deposition and mineralization of both enamel and dentin; (2) high levels of medium Ca induce hypermineralization of enamel and give rise to deposition of a more irregular enamel than at moderate Ca levels; and (3) high levels of P are not able to induce mineralization when Ca levels are low but seem to moderate effects of moderate and high levels of Ca.


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