Literature DB >> 3361117

Enkephalins in human phaeochromocytomas: localization in immunoreactive, high molecular weight form to the soluble core of chromaffin granules.

R J Parmer1, D T O'Connor.   

Abstract

Enkephalins, endogenous opioid pentapeptides, are found in normal chromaffin tissue and may influence blood pressure regulation. We studied the subcellular localization and precursor-product status of enkephalin immunoreactivity in 11 human phaeochromocytomas (seven adrenal, four extra-adrenal). Enkephalin immunoreactivity was found in all phaeochromocytomas, it paralleled radio-immunoassay standard curves and was not destroyed by boiling or protease inhibitors i.e. ethylenediaminetetraacetic acid (EDTA) and phenylmethylsulfonyl fluoride (PMSF). Sucrose gradients localized enkephalin immunoreactivity to chromaffin granules (55 +/- 17% of total immunoreactivity; n = 6). In vitro granule lysis released 81% of the enkephalins and 91% of the catecholamines. Thus, phaeochromocytoma enkephalins are present in the soluble core of chromaffin granules, along with catecholamines. Enkephalin immunoreactivity was not contained in purified chromogranin A, either before or after trypsin cleavage. High pressure liquid chromatography (HPLC) elution of enkephalin immunoreactivity matched that of synthetic methionine-enkephalin, leucine-enkephalin, and methionine-sulfoxide-enkephalin standards. Enkephalin immunoreactivity was augmented by trypsin alone and by trypsin plus carboxypeptidase B (by 352 +/- 56%), suggesting that the majority of the enkephalins were present in higher molecular weight precursor form. Sephacryl S-200 gel filtration of chromaffin granule lysate revealed a trypsin-augmented putative human enkephalin precursor with a molecular weight of 2000-4000 daltons as well as product enkephalins. Enkephalin concentration in phaeochromocytoma closely paralleled the epinephrine, but not the norepinephrine content of the tumours. However, it was not statistically different in adrenal versus extra-adrenal tumours. Thus, these peptides are contained in high molecular weight form in the soluble core of catecholamine storage vesicles, predominantly epinephrine vesicles.

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Year:  1988        PMID: 3361117     DOI: 10.1097/00004872-198803000-00002

Source DB:  PubMed          Journal:  J Hypertens        ISSN: 0263-6352            Impact factor:   4.844


  5 in total

1.  Augmented enkephalin-immunoreactivity in adrenaline-producing phaeochromocytomas.

Authors:  T Kodama; C Ito; Y Fujimoto; Y Ito; T Obara; A Hirayama
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1990

2.  Secretory protein traffic. Chromogranin A contains a dominant targeting signal for the regulated pathway.

Authors:  R J Parmer; X P Xi; H J Wu; L J Helman; L N Petz
Journal:  J Clin Invest       Date:  1993-08       Impact factor: 14.808

Review 3.  Diseases of the adrenal medulla.

Authors:  M M Fung; O H Viveros; D T O'Connor
Journal:  Acta Physiol (Oxf)       Date:  2007-11-16       Impact factor: 6.311

4.  Naturally occurring human genetic variation in the 3'-untranslated region of the secretory protein chromogranin A is associated with autonomic blood pressure regulation and hypertension in a sex-dependent fashion.

Authors:  Yuqing Chen; Fangwen Rao; Juan L Rodriguez-Flores; Manjula Mahata; Maple M Fung; Mats Stridsberg; Sucheta M Vaingankar; Gen Wen; Rany M Salem; Madhusudan Das; Myles G Cockburn; Nicholas J Schork; Michael G Ziegler; Bruce A Hamilton; Sushil K Mahata; Laurent Taupenot; Daniel T O'Connor
Journal:  J Am Coll Cardiol       Date:  2008-10-28       Impact factor: 24.094

5.  The protein architecture of human secretory vesicles reveals differential regulation of signaling molecule secretion by protein kinases.

Authors:  Steven J Bark; Jill Wegrzyn; Laurent Taupenot; Michael Ziegler; Daniel T O'Connor; Qi Ma; Michael Smoot; Trey Ideker; Vivian Hook
Journal:  PLoS One       Date:  2012-08-16       Impact factor: 3.240

  5 in total

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