WE-14, a chromogranin A - Derived neuropeptide
(2002) In Annals of the New York Academy of Sciences 971. p.311-316- Abstract
- The neuropeptide WE-14 is derived from the posttranslational processing of chromogranin A (CgA). While CgA is expressed in a preponderance of neuroendocrine cells, WE-14 is generated in a distinct subpopulation of CgA-immunopositive cells, most notably in the adrenal, pituitary, and parathyroid glands. Physiological and pharmacological studies have demonstrated that CgA is cleaved to generate WE-14 in the adrenal chromaffin cell population and in the enterochromaffin-like (ECL) cells of the oxyntic mucosa. Pathological analyses of neuroendocrine tumors have revealed a heterogeneous pattern of WE-14 immunostaining, with variable concentrations quantified and chromatographically resolved in tissue extracts. Phylogenetic surveys have... (More)
- The neuropeptide WE-14 is derived from the posttranslational processing of chromogranin A (CgA). While CgA is expressed in a preponderance of neuroendocrine cells, WE-14 is generated in a distinct subpopulation of CgA-immunopositive cells, most notably in the adrenal, pituitary, and parathyroid glands. Physiological and pharmacological studies have demonstrated that CgA is cleaved to generate WE-14 in the adrenal chromaffin cell population and in the enterochromaffin-like (ECL) cells of the oxyntic mucosa. Pathological analyses of neuroendocrine tumors have revealed a heterogeneous pattern of WE-14 immunostaining, with variable concentrations quantified and chromatographically resolved in tissue extracts. Phylogenetic surveys have demonstrated that WE-14 exhibits an ancient lineage, while ontogenetic examination has shown that it is generated at an early stage during fetal development. Putative WE-14 receptor binding sites have been identified in several tissues; however, the physiological role of WE-14 remains enigmatic. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/322676
- author
- Curry, WJ ; Barkatullah, SC ; Johansson, AN ; Quinn, JG ; Norlén, Per LU ; Connolly, CK ; McCollum, AP and McVicar, CM
- organization
- publishing date
- 2002
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- WE-14, chromogranin A
- in
- Annals of the New York Academy of Sciences
- volume
- 971
- pages
- 311 - 316
- publisher
- Wiley-Blackwell
- external identifiers
-
- wos:000179509100060
- pmid:12438141
- scopus:0037024629
- ISSN
- 0077-8923
- language
- English
- LU publication?
- yes
- id
- 2595ecce-f7ba-4d5d-91c4-38d1ab172c07 (old id 322676)
- alternative location
- http://www.annalsnyas.org/cgi/content/abstract/971/1/311
- date added to LUP
- 2016-04-01 16:09:12
- date last changed
- 2022-01-28 17:39:10
@article{2595ecce-f7ba-4d5d-91c4-38d1ab172c07, abstract = {{The neuropeptide WE-14 is derived from the posttranslational processing of chromogranin A (CgA). While CgA is expressed in a preponderance of neuroendocrine cells, WE-14 is generated in a distinct subpopulation of CgA-immunopositive cells, most notably in the adrenal, pituitary, and parathyroid glands. Physiological and pharmacological studies have demonstrated that CgA is cleaved to generate WE-14 in the adrenal chromaffin cell population and in the enterochromaffin-like (ECL) cells of the oxyntic mucosa. Pathological analyses of neuroendocrine tumors have revealed a heterogeneous pattern of WE-14 immunostaining, with variable concentrations quantified and chromatographically resolved in tissue extracts. Phylogenetic surveys have demonstrated that WE-14 exhibits an ancient lineage, while ontogenetic examination has shown that it is generated at an early stage during fetal development. Putative WE-14 receptor binding sites have been identified in several tissues; however, the physiological role of WE-14 remains enigmatic.}}, author = {{Curry, WJ and Barkatullah, SC and Johansson, AN and Quinn, JG and Norlén, Per and Connolly, CK and McCollum, AP and McVicar, CM}}, issn = {{0077-8923}}, keywords = {{WE-14; chromogranin A}}, language = {{eng}}, pages = {{311--316}}, publisher = {{Wiley-Blackwell}}, series = {{Annals of the New York Academy of Sciences}}, title = {{WE-14, a chromogranin A - Derived neuropeptide}}, url = {{http://www.annalsnyas.org/cgi/content/abstract/971/1/311}}, volume = {{971}}, year = {{2002}}, }