Cloning and characterization of an abundant subtype of the human calcitonin receptor

Rolf E. Kuestner, Racheal D. Elrod, Francis J. Grant, Frederick S. Hagen, Joseph L. Kuijper, Shannon L. Matthewes, Patrick J. O'Hara, Paul O. Sheppard, Steven D. Stroop, Deborah L. Thompson, Theodore E. Whitmore, David M. Findlay, Souheir Houssami, Patrick M. Sexton, Emma E. Moore

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Abstract

We have cloned and characterized a second form of the human calcitonin receptor from T47D cells. It resembles the clone described by Gorn et al. [J. Clin. Invest. 90:1726-1735 (1992)] except that it lacks a 16-amino acid insert in the putative first intracellular loop. The insert-negative receptor appears to be the most abundant form, and it occurs at a relatively constant level in all expressing tissues. In contrast, the insert-positive receptor is found at low levels in most tissues but its expression levels appear to be much more variable. The insert-negative cDNA was stably expressed in baby hamster kidney cells. Like the endogenous T47D receptor, the recombinant receptor has an equally high affinity for salmon and porcine calcitonin but a 3-4-fold lower affinity for human calcitonin. High concentrations of calcitonin gene-related peptide, rat amylin, secretin, or vasoactive intestinal peptide do not significantly compete with calcitonin for binding to the recombinant receptor. Calcitonin stimulates a cAMP response in both T47D and transfected baby hamster kidney cells. Salmon calcitonin is more potent than human calcitonin for T47D cells, but the two are nearly equipotent for the transfectants. Furthermore, the ED 50 for the cAMP response in the transfectants is 10-100-fold lower than in T47D cells. Calcitonin stimulates inositol phosphate turnover and elevates internal calcium levels in the transfectants. This response requires non-physiological levels of calcitonin and is directly correlated with the number of receptors. Lastly, by using a human/rodent somatic cell hybrid panel and in situ hybridization, we localized the human calcitonin receptor gene to chromosome 7.

Original languageEnglish
Pages (from-to)246-255
Number of pages10
JournalMolecular Pharmacology
Volume46
Issue number2
Publication statusPublished - 1 Aug 1994
Externally publishedYes

Cite this

Kuestner, R. E., Elrod, R. D., Grant, F. J., Hagen, F. S., Kuijper, J. L., Matthewes, S. L., ... Moore, E. E. (1994). Cloning and characterization of an abundant subtype of the human calcitonin receptor. Molecular Pharmacology, 46(2), 246-255.
Kuestner, Rolf E. ; Elrod, Racheal D. ; Grant, Francis J. ; Hagen, Frederick S. ; Kuijper, Joseph L. ; Matthewes, Shannon L. ; O'Hara, Patrick J. ; Sheppard, Paul O. ; Stroop, Steven D. ; Thompson, Deborah L. ; Whitmore, Theodore E. ; Findlay, David M. ; Houssami, Souheir ; Sexton, Patrick M. ; Moore, Emma E. / Cloning and characterization of an abundant subtype of the human calcitonin receptor. In: Molecular Pharmacology. 1994 ; Vol. 46, No. 2. pp. 246-255.
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title = "Cloning and characterization of an abundant subtype of the human calcitonin receptor",
abstract = "We have cloned and characterized a second form of the human calcitonin receptor from T47D cells. It resembles the clone described by Gorn et al. [J. Clin. Invest. 90:1726-1735 (1992)] except that it lacks a 16-amino acid insert in the putative first intracellular loop. The insert-negative receptor appears to be the most abundant form, and it occurs at a relatively constant level in all expressing tissues. In contrast, the insert-positive receptor is found at low levels in most tissues but its expression levels appear to be much more variable. The insert-negative cDNA was stably expressed in baby hamster kidney cells. Like the endogenous T47D receptor, the recombinant receptor has an equally high affinity for salmon and porcine calcitonin but a 3-4-fold lower affinity for human calcitonin. High concentrations of calcitonin gene-related peptide, rat amylin, secretin, or vasoactive intestinal peptide do not significantly compete with calcitonin for binding to the recombinant receptor. Calcitonin stimulates a cAMP response in both T47D and transfected baby hamster kidney cells. Salmon calcitonin is more potent than human calcitonin for T47D cells, but the two are nearly equipotent for the transfectants. Furthermore, the ED 50 for the cAMP response in the transfectants is 10-100-fold lower than in T47D cells. Calcitonin stimulates inositol phosphate turnover and elevates internal calcium levels in the transfectants. This response requires non-physiological levels of calcitonin and is directly correlated with the number of receptors. Lastly, by using a human/rodent somatic cell hybrid panel and in situ hybridization, we localized the human calcitonin receptor gene to chromosome 7.",
author = "Kuestner, {Rolf E.} and Elrod, {Racheal D.} and Grant, {Francis J.} and Hagen, {Frederick S.} and Kuijper, {Joseph L.} and Matthewes, {Shannon L.} and O'Hara, {Patrick J.} and Sheppard, {Paul O.} and Stroop, {Steven D.} and Thompson, {Deborah L.} and Whitmore, {Theodore E.} and Findlay, {David M.} and Souheir Houssami and Sexton, {Patrick M.} and Moore, {Emma E.}",
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Kuestner, RE, Elrod, RD, Grant, FJ, Hagen, FS, Kuijper, JL, Matthewes, SL, O'Hara, PJ, Sheppard, PO, Stroop, SD, Thompson, DL, Whitmore, TE, Findlay, DM, Houssami, S, Sexton, PM & Moore, EE 1994, 'Cloning and characterization of an abundant subtype of the human calcitonin receptor', Molecular Pharmacology, vol. 46, no. 2, pp. 246-255.

Cloning and characterization of an abundant subtype of the human calcitonin receptor. / Kuestner, Rolf E.; Elrod, Racheal D.; Grant, Francis J.; Hagen, Frederick S.; Kuijper, Joseph L.; Matthewes, Shannon L.; O'Hara, Patrick J.; Sheppard, Paul O.; Stroop, Steven D.; Thompson, Deborah L.; Whitmore, Theodore E.; Findlay, David M.; Houssami, Souheir; Sexton, Patrick M.; Moore, Emma E.

In: Molecular Pharmacology, Vol. 46, No. 2, 01.08.1994, p. 246-255.

Research output: Contribution to journalArticleResearchpeer-review

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T1 - Cloning and characterization of an abundant subtype of the human calcitonin receptor

AU - Kuestner, Rolf E.

AU - Elrod, Racheal D.

AU - Grant, Francis J.

AU - Hagen, Frederick S.

AU - Kuijper, Joseph L.

AU - Matthewes, Shannon L.

AU - O'Hara, Patrick J.

AU - Sheppard, Paul O.

AU - Stroop, Steven D.

AU - Thompson, Deborah L.

AU - Whitmore, Theodore E.

AU - Findlay, David M.

AU - Houssami, Souheir

AU - Sexton, Patrick M.

AU - Moore, Emma E.

PY - 1994/8/1

Y1 - 1994/8/1

N2 - We have cloned and characterized a second form of the human calcitonin receptor from T47D cells. It resembles the clone described by Gorn et al. [J. Clin. Invest. 90:1726-1735 (1992)] except that it lacks a 16-amino acid insert in the putative first intracellular loop. The insert-negative receptor appears to be the most abundant form, and it occurs at a relatively constant level in all expressing tissues. In contrast, the insert-positive receptor is found at low levels in most tissues but its expression levels appear to be much more variable. The insert-negative cDNA was stably expressed in baby hamster kidney cells. Like the endogenous T47D receptor, the recombinant receptor has an equally high affinity for salmon and porcine calcitonin but a 3-4-fold lower affinity for human calcitonin. High concentrations of calcitonin gene-related peptide, rat amylin, secretin, or vasoactive intestinal peptide do not significantly compete with calcitonin for binding to the recombinant receptor. Calcitonin stimulates a cAMP response in both T47D and transfected baby hamster kidney cells. Salmon calcitonin is more potent than human calcitonin for T47D cells, but the two are nearly equipotent for the transfectants. Furthermore, the ED 50 for the cAMP response in the transfectants is 10-100-fold lower than in T47D cells. Calcitonin stimulates inositol phosphate turnover and elevates internal calcium levels in the transfectants. This response requires non-physiological levels of calcitonin and is directly correlated with the number of receptors. Lastly, by using a human/rodent somatic cell hybrid panel and in situ hybridization, we localized the human calcitonin receptor gene to chromosome 7.

AB - We have cloned and characterized a second form of the human calcitonin receptor from T47D cells. It resembles the clone described by Gorn et al. [J. Clin. Invest. 90:1726-1735 (1992)] except that it lacks a 16-amino acid insert in the putative first intracellular loop. The insert-negative receptor appears to be the most abundant form, and it occurs at a relatively constant level in all expressing tissues. In contrast, the insert-positive receptor is found at low levels in most tissues but its expression levels appear to be much more variable. The insert-negative cDNA was stably expressed in baby hamster kidney cells. Like the endogenous T47D receptor, the recombinant receptor has an equally high affinity for salmon and porcine calcitonin but a 3-4-fold lower affinity for human calcitonin. High concentrations of calcitonin gene-related peptide, rat amylin, secretin, or vasoactive intestinal peptide do not significantly compete with calcitonin for binding to the recombinant receptor. Calcitonin stimulates a cAMP response in both T47D and transfected baby hamster kidney cells. Salmon calcitonin is more potent than human calcitonin for T47D cells, but the two are nearly equipotent for the transfectants. Furthermore, the ED 50 for the cAMP response in the transfectants is 10-100-fold lower than in T47D cells. Calcitonin stimulates inositol phosphate turnover and elevates internal calcium levels in the transfectants. This response requires non-physiological levels of calcitonin and is directly correlated with the number of receptors. Lastly, by using a human/rodent somatic cell hybrid panel and in situ hybridization, we localized the human calcitonin receptor gene to chromosome 7.

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Kuestner RE, Elrod RD, Grant FJ, Hagen FS, Kuijper JL, Matthewes SL et al. Cloning and characterization of an abundant subtype of the human calcitonin receptor. Molecular Pharmacology. 1994 Aug 1;46(2):246-255.