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Bombesin receptors in a human duodenal tumor cell line: binding properties and function
1Department of Pharmacology, University of Texas Medical School, Houston 77225.
Abstract:
The bombesin family of peptides elicit numerous biological responses in the gut, including stimulation of cell proliferation, and have been implicated as growth factors in a variety of gastrointestinal tumors. Even though these peptides and their receptors are distributed throughout the gastrointestinal tract, there are few cell lines available as model systems to study bombesin action in gastrointestinal cells. In this study, we have characterized functional bombesin receptors in a human duodenal cancer cell line, HuTu-80. The binding of [125I-Tyr4]bombesin to intact cells at 4 degrees C reached equilibrium by 6 h. Scatchard analysis of [125I-Tyr4]bombesin binding showed that HuTu-80 cells contained a single class of high affinity binding sites (5900 +/- 1960/cell; Kd = 80 +/- 20 pM). [125I-Tyr4]bombesin binding was inhibited by bombesin receptor agonists and antagonists with the following order of potencies: gastrin-releasing peptide (GRP) = GRP-(14-27) = bombesin > [DPhe6]bombesin(6-13)ethylamide > [Leu13 psi-(CH2NH)Leu14]bombesin > neuromedin B. Photoaffinity cross-linking studies, in which N-5-azido-2-nitrobenzoyloxysuccinimide was used to covalently couple [125I]GRP(14-27) to cells at 4 degrees C, resulted in the specific labeling of a broad band with an apparent molecular mass of 66,000 daltons. Consistent with the presence of high affinity receptors, bombesin increased the formation of inositol phosphates in HuTu-80 cells in a dose-dependent manner (concentration eliciting half-maximal effect, 290 +/- 70 pM). However, under conditions where both insulin and serum increased [3H]thymidine incorporation into DNA, 10 nM bombesin had no effect either alone or in the presence of insulin. Bombesin also had no effect on colony formation by HuTu-80 cells in soft agar. Furthermore, the bombesin receptor antagonist, [Leu13 psi(CH2NH)Leu14]bombesin, did not inhibit [3H]thymidine incorporation or clonal growth either in the absence or in the presence of serum. Together, these results show that HuTu-80 cells contain high affinity bombesin receptors of the GRP subtype. These receptors are functionally coupled to second messenger production but do not stimulate cell proliferation.
Insights
This study identifies functional bombesin receptors in HuTu-80 duodenal cancer cells. These receptors activate signaling pathways but do not promote cell proliferation, offering insights into gastrointestinal tumor research.
Area of Science:
- Gastroenterology
- Molecular Biology
- Oncology
Background:
- Bombesin peptides stimulate gut cell proliferation and are implicated in gastrointestinal tumors.
- Limited cell line models exist for studying bombesin action in gastrointestinal cells.
Purpose of the Study:
- To characterize functional bombesin receptors in the human duodenal cancer cell line, HuTu-80.
- To investigate the role of bombesin receptors in HuTu-80 cell proliferation and growth.
Main Methods:
- Radioligand binding assays using [125I-Tyr4]bombesin to determine receptor affinity and density.
- Scatchard analysis to quantify binding sites.
- Photoaffinity cross-linking to identify receptor molecular mass.
- Measurement of inositol phosphate production and [3H]thymidine incorporation.
Main Results:
- HuTu-80 cells possess high-affinity bombesin receptors (Kd = 80 +/- 20 pM) of the gastrin-releasing peptide (GRP) subtype.
- Bombesin binding was inhibited by GRP and its analogs, with specific labeling of a 66 kDa protein.
- Bombesin stimulated inositol phosphate production but did not affect [3H]thymidine incorporation or colony formation.
Conclusions:
- HuTu-80 cells express functional, high-affinity GRP-subtype bombesin receptors.
- These receptors are coupled to second messenger production but do not drive cell proliferation in this model.
- This cell line serves as a valuable tool for studying bombesin receptor signaling independent of proliferative effects.
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