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Differentiation of the chick oviduct in vitro Vanderhorst, Elizabeth Wilhelmina Maria
Abstract
Immature chick oviducts differentiate in vivo in response to daily injections of DES. This is indicated by increases in general oviduct protein nitrogen: DNA ratios and the production of immunologically precipitable ovalbumin. Three types of ovalbumin are produced in response to estrogen. These results indicate that ovalbumin free of phosphorus appears first in the oviduct tissue in response to DES. The appearance of phosphorus containing ovalbumin follows. Attempts were made to induce the in vitro differentiation of oviduct tissue under a variety of culture conditions. A standard culture media was supplemented with DES and serum (fetal calf, cockerel, laying hen, or chick serum) as well as serum from DES injected chicks. No changes were observed in the tissue histology nor in the production of the specific protein, ovalbumin, under the above conditions. Closely associated tissues such as kidneys, ovaries, mesentary or ureter tissue cultured with the oviduct tissue failed to elicite any detectible morphological and chemical changes in the latter. The addition of insulin or homogenized pituitaries from DES injected or non-injected chicks was ineffective as an inducer of differentiation in this system. Substituting 17 6-estradiol for DES as an inducer did not alter the results. Thus, with the exception of estrogen any factor(s) necessary for the in vivo differentiation of immature oviduct tissue remains unknown at this time.
Item Metadata
Title |
Differentiation of the chick oviduct in vitro
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Creator | |
Publisher |
University of British Columbia
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Date Issued |
1972
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Description |
Immature chick oviducts differentiate in vivo in response to daily injections of DES. This is indicated by increases in general oviduct protein nitrogen: DNA ratios and the production of immunologically precipitable ovalbumin. Three types of ovalbumin are produced in response to estrogen. These results indicate that ovalbumin free of phosphorus appears first in the oviduct tissue in response to DES. The appearance of phosphorus containing ovalbumin follows.
Attempts were made to induce the in vitro differentiation
of oviduct tissue under a variety of culture conditions.
A standard culture media was supplemented with DES and serum (fetal calf, cockerel, laying hen, or chick serum) as well as serum from DES injected chicks. No changes were observed in the tissue histology nor in the production of the specific protein, ovalbumin, under the above conditions.
Closely associated tissues such as kidneys, ovaries, mesentary or ureter tissue cultured with the oviduct tissue failed to elicite any detectible morphological and chemical changes in the latter. The addition of insulin or homogenized pituitaries from DES injected or non-injected chicks was ineffective as an inducer of differentiation in this system.
Substituting 17 6-estradiol for DES as an inducer did not alter the results.
Thus, with the exception of estrogen any factor(s) necessary for the in vivo differentiation of immature oviduct tissue remains unknown at this time.
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Genre | |
Type | |
Language |
eng
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Date Available |
2011-04-07
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Provider |
Vancouver : University of British Columbia Library
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Rights |
For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use.
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DOI |
10.14288/1.0101584
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URI | |
Degree | |
Program | |
Affiliation | |
Degree Grantor |
University of British Columbia
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Campus | |
Scholarly Level |
Graduate
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Aggregated Source Repository |
DSpace
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Item Media
Item Citations and Data
Rights
For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use.