Functional expression of TRPM7 as a Ca2+ influx pathway in adipocytes. Issue 20 (24th October 2019)
- Record Type:
- Journal Article
- Title:
- Functional expression of TRPM7 as a Ca2+ influx pathway in adipocytes. Issue 20 (24th October 2019)
- Main Title:
- Functional expression of TRPM7 as a Ca2+ influx pathway in adipocytes
- Authors:
- Inoue, Hana
Inazu, Masato
Konishi, Masato
Yokoyama, Utako - Abstract:
- Abstract: In adipocytes, intracellular Ca 2+ and Mg 2+ modulates physiological functions, such as insulin action and the secretion of adipokines. TRPM7 is a Ca 2+ /Mg 2+ ‐permeable non‐selective cation channel. TRPM7 mRNA is highly expressed in adipose tissue, however, its functional expression in adipocytes remains to be elucidated. In this study, we demonstrated for the first time that TRPM7 was functionally expressed in both freshly isolated white adipocytes and in 3T3‐L1 adipocytes differentiated from a 3T3‐L1 pre‐adipocyte cell line by whole‐cell patch‐clamp recordings. Consistent with known properties of TRPM7 current, the current in adipocytes was activated by the elimination of extracellular divalent cations and the reduction of intracellular free Mg 2+ concentrations, and was inhibited by the TRPM7 inhibitors, 2‐aminoethyl diphenylborinate (2‐APB), hydrogen peroxide (H2 O2 ), N‐methyl maleimide (NMM), NS8593, and 2‐amino‐2‐[2‐(4‐octylphenyl)ethyl]‐1, 3‐propanediol (FTY720). Treatment with small‐interfering (si) RNA targeting TRPM7 resulted in a reduction in the current to 23 ± 7% of nontargeting siRNA‐treated adipocytes. Moreover a TRPM7 activator, naltriben, increased the TRPM7‐like current and [Ca 2+ ]i in 3T3‐L1 adipocytes but not in TRPM7‐knockdown adipocytes. These findings indicate that TRPM7 is functionally expressed, and plays a role as a Ca 2+ influx pathway in adipocytes. Abstract : We demonstrate the functional expression of TRPM7 in native whiteAbstract: In adipocytes, intracellular Ca 2+ and Mg 2+ modulates physiological functions, such as insulin action and the secretion of adipokines. TRPM7 is a Ca 2+ /Mg 2+ ‐permeable non‐selective cation channel. TRPM7 mRNA is highly expressed in adipose tissue, however, its functional expression in adipocytes remains to be elucidated. In this study, we demonstrated for the first time that TRPM7 was functionally expressed in both freshly isolated white adipocytes and in 3T3‐L1 adipocytes differentiated from a 3T3‐L1 pre‐adipocyte cell line by whole‐cell patch‐clamp recordings. Consistent with known properties of TRPM7 current, the current in adipocytes was activated by the elimination of extracellular divalent cations and the reduction of intracellular free Mg 2+ concentrations, and was inhibited by the TRPM7 inhibitors, 2‐aminoethyl diphenylborinate (2‐APB), hydrogen peroxide (H2 O2 ), N‐methyl maleimide (NMM), NS8593, and 2‐amino‐2‐[2‐(4‐octylphenyl)ethyl]‐1, 3‐propanediol (FTY720). Treatment with small‐interfering (si) RNA targeting TRPM7 resulted in a reduction in the current to 23 ± 7% of nontargeting siRNA‐treated adipocytes. Moreover a TRPM7 activator, naltriben, increased the TRPM7‐like current and [Ca 2+ ]i in 3T3‐L1 adipocytes but not in TRPM7‐knockdown adipocytes. These findings indicate that TRPM7 is functionally expressed, and plays a role as a Ca 2+ influx pathway in adipocytes. Abstract : We demonstrate the functional expression of TRPM7 in native white adipocytes and 3T3‐L1 adipocytes by patch‐clamp recordings. Activation of TRPM7 increased in intracellular [Ca 2+ ] in adipocytes. It is suggeted that TRPM7 may modulate physiological functions of adipocytes via permeating Ca 2+ . … (more)
- Is Part Of:
- Physiological reports. Volume 7:Issue 20(2019)
- Journal:
- Physiological reports
- Issue:
- Volume 7:Issue 20(2019)
- Issue Display:
- Volume 7, Issue 20 (2019)
- Year:
- 2019
- Volume:
- 7
- Issue:
- 20
- Issue Sort Value:
- 2019-0007-0020-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2019-10-24
- Subjects:
- Adipocyte -- calcium pathway -- TRP channel -- TRPM7
Physiology -- Periodicals
571 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2051-817X ↗
http://physreports.physiology.org ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.14814/phy2.14272 ↗
- Languages:
- English
- ISSNs:
- 2051-817X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 12056.xml