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Expression of two glycoprotein hormone receptors in larval, parasitic phase, and adult sea lampreys. | LitMetric

Expression of two glycoprotein hormone receptors in larval, parasitic phase, and adult sea lampreys.

Gen Comp Endocrinol

Center for Molecular and Comparative Endocrinology and Department of Molecular, Cellular, and Biomedical Sciences, University of New Hampshire, Durham, NH 03824, USA. Electronic address:

Published: August 2018

AI Article Synopsis

  • Jawed vertebrates, including humans, have three key glycoprotein hormones and corresponding receptors, while the sea lamprey has only two unique glycoprotein hormones and receptors.
  • Research using advanced techniques revealed that the receptors are expressed in specific organs like ovaries and thyroids throughout different life stages of the lamprey.
  • Administering lamprey gonadotropin-releasing hormones increased receptor expression and estradiol levels, but did not significantly affect ovarian receptor expression, indicating potential differences in how the hormones function in lampreys.

Article Abstract

All jawed vertebrates have three canonical glycoprotein hormones (GpHs: luteinizing hormone, LH; follicle stimulating hormone, FSH; and thyroid stimulating hormone, TSH) with three corresponding GpH receptors (GpH-Rs: LH-R, FSH-R, and TSH-R). In contrast, we propose that the jawless vertebrate, the sea lamprey (Petromyzon marinus), only has two pituitary glycoprotein hormones, lamprey (l)GpH and l-thyrostimulin, and two functional glycoprotein receptors, lGpH-R I and II. It is not known at this time whether there is a specific receptor for lGpH and l-thyrostimulin, or if both GpHs can differentially activate the lGpH-Rs. In this report, we determined the RNA expression of lGpH-R I and II in the gonads and thyroids of larval, parasitic phase, and adult lampreys. A highly sensitive dual-label fluorescent in situ hybridization technique (RNAScope™) showed lGpH-R I expression in the ovaries of larval lamprey, and co-localization and co-expression of lGpH-R I and II in the ovaries of parasitic phase and adult lampreys. Both receptors were also highly co-localized and co-expressed in the endostyle of larval lamprey and thyroid follicles of parasitic and adult lampreys. In addition, we performed in vivo studies to determine the actions of lamprey gonadotropin releasing hormones (lGnRHs) on lGpH-R I and II expression by real time PCR, and determined plasma concentrations of estradiol and thyroxine. Administration of lGnRH-III significantly (p ≤ 0.01) increased lGpHR II expression in the thyroid follicles of adult female lampreys but did not cause a significant increase in RNA expression of lGpH-R I and II in ovaries. Concomitantly, there was a significant increase (p ≤ 0.01) of plasma estradiol without any significant changes of plasma thyroxine concentrations in response to treatment to lGnRH-I, -II, or -III. In summary, our results provide supporting evidence that the lamprey pituitary glycoprotein hormones may differentially activate the lamprey GpH-Rs in regulating both thyroid and gonadal activities during each of the three life stages of the sea lamprey.

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Source
http://dx.doi.org/10.1016/j.ygcen.2017.11.006DOI Listing

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