Creatine biosynthesis and transport by the term human placenta. (April 2017)
- Record Type:
- Journal Article
- Title:
- Creatine biosynthesis and transport by the term human placenta. (April 2017)
- Main Title:
- Creatine biosynthesis and transport by the term human placenta
- Authors:
- Ellery, Stacey J.
Della Gatta, Paul A.
Bruce, Clinton R.
Kowalski, Greg M.
Davies-Tuck, Miranda
Mockler, Joanne C.
Murthi, Padma
Walker, David W.
Snow, Rod J.
Dickinson, Hayley - Abstract:
- Abstract: Introduction: Creatine is an amino acid derivative that is involved in preserving ATP homeostasis. Previous studies suggest an important role for the creatine kinase circuit for placental ATP turnover. Creatine is obtained from both the diet and endogenous synthesis, usually along the renal-hepatic axis. However, some tissues with a high-energy demand have an inherent capacity to synthesise creatine. In this study, we determined if the term human placenta has the enzymatic machinary to synthesise creatine. Methods: Eleven placentae were collected following elective term caesarean section. Samples from the 4 quadrants of each placenta were either fixed in formalin or frozen. qPCR was used to determine the mRNA expression of the creatine synthesising enzymes arginine:glycine amidinotransferase (AGAT) and guanidinoacetate methyltransferase (GAMT), and the creatine transporter (SLC6A8). Protein expression of AGAT and GAMT was quantified by Western blot, and observations of cell localisation of AGAT, GAMT and SLC6A8 made with immunohistochemistry. Synthesis of guanidinoacetate (GAA; creatine precursor) and creatine in placental homogenates was determined via GC-MS and HPLC, respectively. Results: AGAT, GAMT and SLC6A8 mRNA and protein were detected in the human placenta. AGAT staining was identified in stromal and endothelial cells of the fetal capillaries. GAMT and SLC6A8 staining was localised to the syncytiotrophoblast of the fetal villi. Ex vivo, tissue homogenatesAbstract: Introduction: Creatine is an amino acid derivative that is involved in preserving ATP homeostasis. Previous studies suggest an important role for the creatine kinase circuit for placental ATP turnover. Creatine is obtained from both the diet and endogenous synthesis, usually along the renal-hepatic axis. However, some tissues with a high-energy demand have an inherent capacity to synthesise creatine. In this study, we determined if the term human placenta has the enzymatic machinary to synthesise creatine. Methods: Eleven placentae were collected following elective term caesarean section. Samples from the 4 quadrants of each placenta were either fixed in formalin or frozen. qPCR was used to determine the mRNA expression of the creatine synthesising enzymes arginine:glycine amidinotransferase (AGAT) and guanidinoacetate methyltransferase (GAMT), and the creatine transporter (SLC6A8). Protein expression of AGAT and GAMT was quantified by Western blot, and observations of cell localisation of AGAT, GAMT and SLC6A8 made with immunohistochemistry. Synthesis of guanidinoacetate (GAA; creatine precursor) and creatine in placental homogenates was determined via GC-MS and HPLC, respectively. Results: AGAT, GAMT and SLC6A8 mRNA and protein were detected in the human placenta. AGAT staining was identified in stromal and endothelial cells of the fetal capillaries. GAMT and SLC6A8 staining was localised to the syncytiotrophoblast of the fetal villi. Ex vivo, tissue homogenates produce both GAA (4.6 nmol mg protein −1 h −1 ) and creatine (52.8 nmol mg protein −1 h −1 ). Discussion: The term human placenta has the capacity to synthesise creatine. These data present a new understanding of placental energy metabolism. Highlights: Term human placenta produces arginine:glycine amidinotransferase (AGAT). Term human placenta produces guanidinoacetate methyltransferase (GAMT). AGAT is localised in stromal and endothelial cells of the fetal capillaries. GAMT and the creatine transporter are localised to the synctiotrophoblast Ex vivo the term human placenta can synthesise guanidinoacetate and creatine. … (more)
- Is Part Of:
- Placenta. Volume 52(2017:Apr.)
- Journal:
- Placenta
- Issue:
- Volume 52(2017:Apr.)
- Issue Display:
- Volume 52 (2017)
- Year:
- 2017
- Volume:
- 52
- Issue Sort Value:
- 2017-0052-0000-0000
- Page Start:
- 86
- Page End:
- 93
- Publication Date:
- 2017-04
- Subjects:
- Cellular energy -- Pregnancy -- Phosphocreatine -- Creatine kinase
Placenta -- Periodicals
Reproduction -- Periodicals
Placenta -- Periodicals
Placenta -- Périodiques
Reproduction -- Périodiques
612.63 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01434004 ↗
http://www.placentajournal.org/ ↗
http://www.clinicalkey.com/dura/browse/journalIssue/01434004 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/01434004 ↗
http://www.elsevier.com/journals ↗
http://www.harcourt-international.com/journals/plac/ ↗
http://www.idealibrary.com/cgi-bin/links/toc/plac ↗
http://www.harcourt-international.com/journals ↗ - DOI:
- 10.1016/j.placenta.2017.02.020 ↗
- Languages:
- English
- ISSNs:
- 0143-4004
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6506.800000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 839.xml