Chemistry: molecular biology and microbiology – Animal cell – per se ; composition thereof; process of... – Method of culturing cells in suspension
Reexamination Certificate
2002-02-04
2004-06-01
Afremova, Vera (Department: 1651)
Chemistry: molecular biology and microbiology
Animal cell, per se ; composition thereof; process of...
Method of culturing cells in suspension
C435S391000, C435S404000, C435S408000, C435S325000, C435S001100, C600S033000
Reexamination Certificate
active
06743629
ABSTRACT:
FIELD OF THE INVENTION
The present invention relates to a culture medium for the in vitro culture of porcine embryo which is produced in vitro (this culture medium will be referred as in vitro culture medium) and a method for in vitro production of porcine embryo using the said culture medium. More specifically, the invention relates to a culture medium for the in vitro culture of porcine embryo which is produced in vitro (this porcine embryo will be referred as in vitro-produced porcine embryo hereinafter), which can improve the quality of the resulting blastocyst and can also increase the development ratio into fetus and infant (or piglet) after transfer of the blastocyst, and a method for in vitro production of porcine embryo using the culture medium.
BACKGROUND OF THE INVENTION
In vitro maturation and in vitro fertilization oocyte (in vitro-produced embryo) has been used recently for the purpose of breeding and growing superior species in mammals. Additionally, the technique for in vitro producing embryo has also been utilized for the production of transgenic animals or clone animals.
In vitro-produced embryo can be generated for porcine [Theriogenology, Vol. 31, p. 1201-1207, 1989], but the resulting blastocyst is poor in quality, with the total cell number of about 35, which is extremely less compared with that of the in vivo-derived blastocyst at the same stage (total cell number of about 60 to 165).
First success has been attained in the production of piglet, more recently, by transferring a blastocyst to a female pig recipient [Theriogenology, Vol. 53, p. 361, 2000]. However, the number of piglets produced is only one to two, inefficiently. The reason why the technique cannot make a progress may possibly reside in the immaturity of the technique for the in vitro culture of in vitro-produced embryo.
According to the last report by some of the present inventors [Biology of Reproduction, Vol. 60, p. 336-340, 1999], it was verified that the in vitro culture of in vitro-produced embryo for a term as short as one or two days deteriorated the development ratio into fetus and infant after transfer.
For culturing in vitro-produced porcine embryo, the NCSU culture medium [Journal of Reproduction and Fertility Supplement, Vol. 48, p. 61-73, 1993] has been used widely. The culture medium contains glucose as an energy source. Glucose is a great energy source, but a possibility is suggested that the metabolites in the form of peroxide might potentially affect the culturing cell adversely. In embryo, in particular, the metabolites cause a concern of adverse effects on the gene expression and the cell cycle progress.
In such circumstances, it is desired to improve the in vitro culture technique of in vitro-produced porcine embryo.
SUMMARY OF THE INVENTION
An object of the invention is to provide a culture medium for the in vitro culture of in vitro-produced porcine embryo, which can improve the quality of the resulting blastocyst and can also increase the development ratio into fetus and piglet after transfer.
It is another object of the invention to provide a method for in vitro production of porcine embryo using the culture medium, thereby enabling to develop into high-quality blastocyst and also to develop into fetus or piglet after transferring of the blastocyst.
DETAILED DESCRIPTION OF THE INVENTION
So as to attain the objects, the inventors have made investigations and attempts to make a modification of the culture method of the two-day term in the early post-fertilization stage.
The reason why the two-day term in the early stage is targeted has a relation with the effect on the development ratio after transfer as described above and is due to the belief that the two-day term, in case of pig, corresponds to the preliminary stage for the expression of genes intrinsic to embryo, namely the 4-cell stage where the development is found to be arrested. In other words, the inventors have expectantly anticipated that the optimization of the culture method during the term can sufficiently progress subsequent development.
Thus, the inventors have determined to use pyruvic acid and lactic acid as energy sources in place of glucose in the conventional NCSU culture medium. Consequently, the inventors have found that the use of such culture medium containing these substances may possibly improve the quality of the blastocyst recovered by the in vitro culture of in vitro-produced porcine embryo.
Post-fertilization embryo exists in the oviduct in living organisms for the early two days, namely up to the 4-cell stage. Accordingly, the inventors have made attempts to develop a culture method mimicking the environment in the oviduct. The inventors have therefore focused their attention to oviductal epithelium. Oviduct epithelium secretes various factors participated in the cell growth and additionally adjusts the ions in a culture medium owing to the action of the cell itself. Hence, it is believed with higher possibility that so-called oviductal epithelial cell-conditioned culture medium containing oviductal epithelial cells at a dispersed state in the medium mimics in vitro the environment in oviduct, to support the early development.
By transferring the blastocyst recovered from the improved in vitro culture broth into a female pig recipient, finally, the inventors have verified that the developmental competence and transfer efficiency of the embryo has been improved significantly.
The present invention has been achieved, based on these findings.
A first aspect of the present invention relates to a culture medium for the in vitro culture of in vitro-produced porcine embryo, comprises containing lactic acid and pyruvic acid.
A second aspect of the present invention relates to a culture medium for the in vitro culture wherein the culture medium is conditioned with oviductal epithelial cell.
A third aspect of the present invention relates to a method for in vitro culturing of in vitro-produced porcine embryo, comprising culturing an in vitro-produced porcine embryo in the culture medium of the first or second aspect of the invention for 0 to 2 days after fertilization, and subsequently culturing the embryo in a glucose-containing culture medium.
The culture medium for the in vitro culture of the first aspect of the invention will now be described below.
A characteristic of the culture medium is basically comprises the NCSU culture medium, for example NCSU37, from which glucose is preliminarily removed and to which lactic acid and pyruvic acid are added in place of glucose.
The reference [Journal of Reproduction and Fertility Supplement, Vol. 48, p. 61-73, 1993] discloses about the NCSU culture medium and other culture medium for porcine embryo. For general porcine embryo culture, NCSU23 and NCSU37 are used. For culturing in vitro-produced porcine embryo, in particular, these culture medium as well as the M-199 culture medium and the SOF culture medium are used.
Further, sucrose can be used in place of sorbitol used in NCSU37, while taurine and hypotaurine used in NCSU23 can also be used in place of sorbitol.
Salts of lactic acid are used as lactic acid, including for example alkali metal salts such as sodium salt and potassium salt and alkali earth metal salts such as calcium salt. These may be used singly or in combination of two or more thereof.
The content of lactic acid in the culture medium is generally 0.25 to 5.5 &mgr;L/mL, preferably about 0.40 to 1.5 &mgr;L/mL in 60% solution.
As pyruvic acid, further, preference is given to pyruvate salts, particularly sodium pyruvate.
The content of pyruvic acid in the culture medium is 0.009 to 0.036 mg/mL, preferably about 0.010 to 0.025 mg/mL.
As described in the second aspect of the present invention, the culture medium being conditioned with an oviductal epithelial cell is preferably used as the culture medium for the in vitro culture. Specifically, the culture medium contains oviductal epithelial cells at a dispersed state. Thus, the culture medium is referred to as “oviductal epithelial cell-con
Kaneko Hiroyuki
Kikuchi Kazuhiro
Noguchi Junko
Afremova Vera
National Institute of Agrobiological
Oblon & Spivak, McClelland, Maier & Neustadt P.C.
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