Co-Expression of Adaptor Protein FAM159B with Different Markers for Neuroendocrine Cells: An Immunocytochemical and Immunohistochemical Study

Int J Mol Sci. 2022 Nov 4;23(21):13503. doi: 10.3390/ijms232113503.

Abstract

Little is known about the adaptor protein FAM159B. Recently, FAM159B was shown to be particularly expressed in neuroendocrine cells and tissues, such as pancreatic islets and neuroendocrine cells of the bronchopulmonary and gastrointestinal tracts, as well as in different types of neuroendocrine tumours. To gain insights into possible interactions of FAM159B with other proteins and/or receptors, we analysed the co-expression of FAM159B and various neuroendocrine-specific markers in the cancer cell lines BON-1, PC-3, NCI-h82, OH-1, and A431 and also in human pancreatic tissues and pancreatic neuroendocrine tumours. The markers included prominent markers of neuroendocrine differentiation, such as chromogranin A (CgA), neuron-specific enolase (NSE), synaptophysin (SYP), insulinoma-associated protein 1 (INSM1), neural cell adhesion molecule 1 (NCAM1), serotonin (5-HT), somatostatin-14/28 (SST), and several receptors that are typically expressed by neuroendocrine cells, such as dopamine receptor 2 (D2R), somatostatin receptor (SSTR) 1, 2, 3, 4 and 5, and regulator of G-protein signalling 9 (RGS9). FAM159B was expressed evenly throughout the cytosol in all five cancer cell lines. Immunocytochemical and immunohistochemical analyses revealed co-expression of FAM159B with SYP, INSM1, RGS9, D2R, SSTR2, SSTR3, SSTR4, and SSTR5 and strong overlapping co-localisation with NSE. Double-labelling and co-immunoprecipitation Western blot analyses confirmed a direct association between FAM159B and NSE. These results suggest the involvement of FAM159B in several intracellular signalling pathways and a direct or indirect influence on diverse membrane proteins and receptors.

Keywords: FAM159B; RGS9; adaptor protein; antibody; dopamine receptor 2; immunocytochemistry; immunohistochemistry; neuroendocrine marker; somatostatin receptor.

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism
  • Biomarkers, Tumor / metabolism
  • Chromogranin A / genetics
  • Chromogranin A / metabolism
  • Humans
  • Neuroendocrine Cells* / metabolism
  • Neuroendocrine Tumors* / genetics
  • Neuroendocrine Tumors* / metabolism
  • Pancreatic Neoplasms* / pathology
  • Repressor Proteins / metabolism

Substances

  • Biomarkers, Tumor
  • Chromogranin A
  • Adaptor Proteins, Signal Transducing
  • INSM1 protein, human
  • Repressor Proteins

Grants and funding

This research received no external funding.