کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5531864 1401817 2017 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Luteinizing Hormone is an effective replacement for hCG to induce ovulation in Xenopus
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیولوژی سلول
پیش نمایش صفحه اول مقاله
Luteinizing Hormone is an effective replacement for hCG to induce ovulation in Xenopus
چکیده انگلیسی


• Luteinizing Hormone is an effective replacement for hCG in Xenopus.
• Comparison of functional efficacy of different species LH demonstrates that human and ovine work best, with porcine and bovine not as effective.
• J strain X. laevis frogs require slightly less hormone to induce ovulation.
• Eggs from inbred J strain X. laevis are slightly smaller than those from WT frogs.

Injection of human Chorionic Gonadotropin (hCG) directly into the dorsal lymph sac of Xenopus is a commonly used protocol for induction of ovulation, but recent shortages in the stocks of commercially available hCG as well as lack of a well tested alternative have resulted in frustrating experimental delays in laboratories that predominantly use Xenopus in their research. Mammalian Luteinizing Hormones (LH) share structural similarity, functional equivalency, and bind the same receptor as hCG; this suggests that LH may serve as a good alternative to hCG for promoting ovulation in Xenopus. LH has been found to induce maturation of Xenopus oocytes in vitro, but whether it can be used to induce ovulation in vivo has not been examined. Here we compared the ability of four mammalian LH proteins, bovine (bLH), human (hLH), ovine (oLH), porcine (pLH), to induce ovulation in Xenopus when injected into the dorsal lymph sac of sexually mature females. We find that both ovine and human LH, but not bovine or porcine, are good substitutes for hCG for induction of ovulation in WT and J strain Xenopus laevis and Xenopus tropicalis.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Developmental Biology - Volume 426, Issue 2, 15 June 2017, Pages 442–448