PMID- 30719459 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20201001 IS - 2356-6752 (Print) IS - 2314-758X (Electronic) IS - 2314-758X (Linking) VI - 2019 DP - 2019 TI - Age-Dependent Protein Expression of Serine/Threonine Phosphatases and Their Inhibitors in the Human Cardiac Atrium. PG - 2675972 LID - 10.1155/2019/2675972 [doi] LID - 2675972 AB - Heart failure and aging of the heart show many similarities regarding hemodynamic and biochemical parameters. There is evidence that heart failure in experimental animals and humans is accompanied and possibly exacerbated by increased activity of protein phosphatase (PP) 1 and/or 2A. Here, we wanted to study the age-dependent protein expression of major members of the protein phosphatase family in human hearts. Right atrial samples were obtained during bypass surgery. Patients (n=60) were suffering from chronic coronary artery disease (CCS 2-3; New York Heart Association (NYHA) stage 1-3). Age ranged from 48 to 84 years (median 69). All patients included in the study were given beta-adrenoceptor blockers. Other medications included angiotensin-converting enzyme (ACE) or angiotensin-receptor-1 (AT(1)) inhibitors, statins, nitrates, and acetylsalicylic acid (ASS). 100 microg of right atrial homogenates was used for western blotting. Antibodies against catalytic subunits (and their major regulatory proteins) of all presently known cardiac serine/threonine phosphatases were used for antigen detection. In detail, we studied the expression of the catalytic subunit of PP1 (PP1c); I(1) (PP1) and I(2) (PP1), proteins that can inhibit the activity of PP1c; the catalytic subunit of PP2A (PP2Ac); regulatory A-subunit of PP2A (PP2A(A)); regulatory B56alpha-subunit of PP2A (PP2A(B)); I(1) (PP2A) and I(2) (PP2A), inhibitory subunits of PP2A; catalytic and regulatory subunits of calcineurin: PP2B(A) and PP2B(B); PP2C; PP5; and PP6. All data were obtained within the linear range of the assay. There was a significant decline in PP2Ac and I(2) (PP2A) expression in older patients, whereas all other parameters remained unchanged with age. It remains to be elucidated whether the decrease in the protein expression of I(2) (PP2A) might elevate cardiac PP2A activity in a detrimental way or is overcome by a reduced protein expression and thus a reduced activity of PP2Ac. FAU - Gergs, Ulrich AU - Gergs U AUID- ORCID: 0000-0001-6986-485X AD - Institut fur Pharmakologie und Toxikologie, Medizinische Fakultat, Martin-Luther-Universitat Halle-Wittenberg, 06112 Halle (Saale), Germany. FAU - Trapp, Theresa AU - Trapp T AD - Institut fur Pharmakologie und Toxikologie, Medizinische Fakultat, Martin-Luther-Universitat Halle-Wittenberg, 06112 Halle (Saale), Germany. FAU - Bushnaq, Hasan AU - Bushnaq H AD - Klinik fur Herz- und Thoraxchirurgie, Medizinische Fakultat, Martin-Luther-Universitat Halle-Wittenberg, 06097 Halle, Germany. FAU - Simm, Andreas AU - Simm A AD - Klinik fur Herz- und Thoraxchirurgie, Medizinische Fakultat, Martin-Luther-Universitat Halle-Wittenberg, 06097 Halle, Germany. FAU - Silber, Rolf-Edgar AU - Silber RE AD - Klinik fur Herz- und Thoraxchirurgie, Medizinische Fakultat, Martin-Luther-Universitat Halle-Wittenberg, 06097 Halle, Germany. FAU - Neumann, Joachim AU - Neumann J AUID- ORCID: 0000-0001-5018-3851 AD - Institut fur Pharmakologie und Toxikologie, Medizinische Fakultat, Martin-Luther-Universitat Halle-Wittenberg, 06112 Halle (Saale), Germany. LA - eng PT - Journal Article DEP - 20190102 PL - United States TA - Adv Med JT - Advances in medicine JID - 101651448 PMC - PMC6334353 EDAT- 2019/02/06 06:00 MHDA- 2019/02/06 06:01 PMCR- 2019/01/02 CRDT- 2019/02/06 06:00 PHST- 2018/02/21 00:00 [received] PHST- 2018/11/22 00:00 [revised] PHST- 2018/11/29 00:00 [accepted] PHST- 2019/02/06 06:00 [entrez] PHST- 2019/02/06 06:00 [pubmed] PHST- 2019/02/06 06:01 [medline] PHST- 2019/01/02 00:00 [pmc-release] AID - 10.1155/2019/2675972 [doi] PST - epublish SO - Adv Med. 2019 Jan 2;2019:2675972. doi: 10.1155/2019/2675972. eCollection 2019.