JP2014520526A5 - - Google Patents
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- JP2014520526A5 JP2014520526A5 JP2014518556A JP2014518556A JP2014520526A5 JP 2014520526 A5 JP2014520526 A5 JP 2014520526A5 JP 2014518556 A JP2014518556 A JP 2014518556A JP 2014518556 A JP2014518556 A JP 2014518556A JP 2014520526 A5 JP2014520526 A5 JP 2014520526A5
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- mitochondrial
- various embodiments
- cell
- bioenergetic
- oocyte
- Prior art date
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- 230000002611 ovarian Effects 0.000 description 5
- KZNIFHPLKGYRTM-UHFFFAOYSA-N Apigenin Chemical compound C1=CC(O)=CC=C1C1=CC(=O)C2=C(O)C=C(O)C=C2O1 KZNIFHPLKGYRTM-UHFFFAOYSA-N 0.000 description 4
- IQPNAANSBPBGFQ-UHFFFAOYSA-N Luteolin Chemical compound C=1C(O)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(O)C(O)=C1 IQPNAANSBPBGFQ-UHFFFAOYSA-N 0.000 description 4
- 230000002715 bioenergetic Effects 0.000 description 4
- 230000002438 mitochondrial Effects 0.000 description 4
- 210000000287 oocyte Anatomy 0.000 description 4
- 210000001519 tissues Anatomy 0.000 description 4
- BAWFJGJZGIEFAR-NNYOXOHSSA-N Nicotinamide adenine dinucleotide Chemical compound NC(=O)C1=CC=C[N+]([C@H]2[C@@H]([C@H](O)[C@@H](COP([O-])(=O)OP(O)(=O)OC[C@@H]3[C@H]([C@@H](O)[C@@H](O3)N3C4=NC=NC(N)=C4N=C3)O)O2)O)=C1 BAWFJGJZGIEFAR-NNYOXOHSSA-N 0.000 description 3
- 210000004027 cells Anatomy 0.000 description 3
- 238000000338 in vitro Methods 0.000 description 3
- 239000002609 media Substances 0.000 description 3
- FNCOVSWSZZVFBQ-UHFFFAOYSA-N 2-[(4-hydroxyphenyl)methylidene]propanedinitrile Chemical compound OC1=CC=C(C=C(C#N)C#N)C=C1 FNCOVSWSZZVFBQ-UHFFFAOYSA-N 0.000 description 2
- 229940117893 Apigenin Drugs 0.000 description 2
- YBHILYKTIRIUTE-UHFFFAOYSA-N Berberine Chemical compound C1=C2CC[N+]3=CC4=C(OC)C(OC)=CC=C4C=C3C2=CC2=C1OCO2 YBHILYKTIRIUTE-UHFFFAOYSA-N 0.000 description 2
- 229940093265 Berberine Drugs 0.000 description 2
- 210000001185 Bone Marrow Anatomy 0.000 description 2
- 229920000460 Mitochondrial DNA Polymers 0.000 description 2
- 235000008714 apigenin Nutrition 0.000 description 2
- 229930015400 berberine Natural products 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 235000009498 luteolin Nutrition 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000035800 maturation Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229950006238 nadide Drugs 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000002407 ATP formation Effects 0.000 description 1
- ZKHQWZAMYRWXGA-KQYNXXCUSA-N Adenosine triphosphate Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O ZKHQWZAMYRWXGA-KQYNXXCUSA-N 0.000 description 1
- 210000004369 Blood Anatomy 0.000 description 1
- 102100003279 CD38 Human genes 0.000 description 1
- 101700044948 CD38 Proteins 0.000 description 1
- 101700037527 DAZL Proteins 0.000 description 1
- 210000001671 Embryonic Stem Cells Anatomy 0.000 description 1
- 208000007984 Female Infertility Diseases 0.000 description 1
- 210000004700 Fetal Blood Anatomy 0.000 description 1
- 206010021928 Infertility female Diseases 0.000 description 1
- 210000003470 Mitochondria Anatomy 0.000 description 1
- 108020005196 Mitochondrial DNA Proteins 0.000 description 1
- 229940052665 NADH Drugs 0.000 description 1
- 206010033165 Ovarian failure Diseases 0.000 description 1
- IASPBORHOMBZMY-UHFFFAOYSA-N SRT1720 Chemical compound C=1N=C2C=CC=CC2=NC=1C(=O)NC1=CC=CC=C1C(N=C1SC=2)=CN1C=2CN1CCNCC1 IASPBORHOMBZMY-UHFFFAOYSA-N 0.000 description 1
- 241000862969 Stella Species 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000000427 antigen Substances 0.000 description 1
- 102000038129 antigens Human genes 0.000 description 1
- 108091007172 antigens Proteins 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 239000006143 cell culture media Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002512 chemotherapy Methods 0.000 description 1
- 238000005138 cryopreservation Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 230000002708 enhancing Effects 0.000 description 1
- 210000004420 female germ cell Anatomy 0.000 description 1
- 230000004720 fertilization Effects 0.000 description 1
- 230000001605 fetal Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000003325 follicular Effects 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 230000004898 mitochondrial function Effects 0.000 description 1
- 230000000394 mitotic Effects 0.000 description 1
- 231100000539 ovarian failure Toxicity 0.000 description 1
- 239000011886 peripheral blood Substances 0.000 description 1
- 210000000130 stem cell Anatomy 0.000 description 1
- 238000004017 vitrification Methods 0.000 description 1
Description
前述の態様のいずれか、又は本明細書に記載の本発明のいずれかの態様の様々な実施形態では、本発明の組成物は、細胞培地、卵母細胞回収液、卵母細胞洗浄液、卵母細胞体外成熟培地、卵胞体外成熟培地、卵母細胞体外受精培地、ガラス化液及び低温保存液の1つ以上から選択される溶液をさらに含有する。様々な実施形態では、本組成物は、卵巣組織、卵胞、骨髄、臍帯血若しくは末梢血を含有する。他の実施形態では、OSCは、単離された非胚性幹細胞であり、これは、有糸分裂能があり、且つVasa、Oct−4、Dazl、Stella、及び任意選択でステージ特異的胎児抗原の1つ以上を発現する。他の実施形態では、OSCは、卵巣組織から得る。様々な実施形態において、OSCは、非卵巣組織から得る。特定の実施形態では、非卵巣組織は、血液又は骨髄である。様々な実施形態において、細胞は、卵巣幹細胞であり、ここで、細胞は、生体エネルギー物質と接触している。別の実施形態では、接触させた細胞は、増加したミトコンドリアDNAコピー数及び/又は増加したATP生産能力を有する。さらに別の実施形態では、ミトコンドリアの数は、約10%、20%、30%、40%、50%若しくは60%増加する。前述の態様のいずれか、又は本明細書に記載の本発明のいずれかの態様の様々な実施形態において、ミトコンドリア機能の増大は、mtDNA含量、ATP、NAD+/NADH、ミトコンドリア質量、膜電位、並びに既知ミトコンドリア量調節因子の遺伝子発現、及び電子伝達系成分をアッセイすることにより検出する。
CD38を阻害することがわかっている数種の生体エネルギー物質が、ベースライン(DMSOのみ)を超える活性を生成し、プラスの結果として評点されたが、このようなものとして、アピゲニン、ルテオリン、チルホスチン8、ベルベリン及びSRT−1720が挙げられる。従って、これらの生体エネルギー物質は、ミトコンドリアパラメータを有益な様式で増加することがわかった。
アピゲニン、ルテオリン、ベルベリン、及びチルホスチン8などの生体エネルギー物質は、NAD+レベルを高めると共に、ミトコンドリアパラメータを有益な様式で増加することが証明された。一実施形態では、このような物質は、化学療法、老化及び未成熟卵巣不全に関連する雌性不妊の治療のための雌性生殖細胞を増強する上で有用である。
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161502840P | 2011-06-29 | 2011-06-29 | |
US61/502,840 | 2011-06-29 | ||
US201261600529P | 2012-02-17 | 2012-02-17 | |
US61/600,529 | 2012-02-17 | ||
PCT/US2012/033672 WO2013002880A1 (en) | 2011-06-29 | 2012-04-13 | Compositions and methods for enhancing bioenergetic status in female germ cells |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2017116146A Division JP6496359B2 (ja) | 2011-06-29 | 2017-06-13 | 雌性生殖細胞における生体エネルギー状態を増強するための組成物及び方法 |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2014520526A JP2014520526A (ja) | 2014-08-25 |
JP2014520526A5 true JP2014520526A5 (ja) | 2017-08-03 |
JP6284475B2 JP6284475B2 (ja) | 2018-02-28 |
Family
ID=47424472
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2014518556A Expired - Fee Related JP6284475B2 (ja) | 2011-06-29 | 2012-04-13 | 雌性生殖細胞における生体エネルギー状態を増強するための組成物及び方法 |
JP2017116146A Expired - Fee Related JP6496359B2 (ja) | 2011-06-29 | 2017-06-13 | 雌性生殖細胞における生体エネルギー状態を増強するための組成物及び方法 |
JP2018202431A Pending JP2019030326A (ja) | 2011-06-29 | 2018-10-29 | インビボで雌性生殖細胞の生体エネルギー状態を増強するための方法 |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2017116146A Expired - Fee Related JP6496359B2 (ja) | 2011-06-29 | 2017-06-13 | 雌性生殖細胞における生体エネルギー状態を増強するための組成物及び方法 |
JP2018202431A Pending JP2019030326A (ja) | 2011-06-29 | 2018-10-29 | インビボで雌性生殖細胞の生体エネルギー状態を増強するための方法 |
Country Status (13)
Country | Link |
---|---|
US (4) | US9845482B2 (ja) |
EP (2) | EP2726601B1 (ja) |
JP (3) | JP6284475B2 (ja) |
CN (1) | CN103827293A (ja) |
AU (2) | AU2012276038B2 (ja) |
BR (1) | BR112013033797A2 (ja) |
CA (1) | CA2847292A1 (ja) |
EA (1) | EA201490050A1 (ja) |
IL (2) | IL230212B (ja) |
MX (1) | MX356815B (ja) |
UA (1) | UA117448C2 (ja) |
WO (1) | WO2013002880A1 (ja) |
ZA (1) | ZA201309707B (ja) |
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