Functional and molecular characterization of transmembrane intracellular pH regulators in human dental pulp stem cells

Arch Oral Biol. 2018 Jun:90:19-26. doi: 10.1016/j.archoralbio.2018.02.018. Epub 2018 Mar 6.

Abstract

Objective: Homeostasis of intracellular pH (pHi) plays vital roles in many cell functions, such as proliferation, apoptosis, differentiation and metastasis. Thus far, Na+-H+ exchanger (NHE), Na+-HCO3- co-transporter (NBC), Cl-/HCO3- exchanger (AE) and Cl-/OH- exchanger (CHE) have been identified to co-regulate pHi homeostasis. However, functional and biological pHi-regulators in human dental pulp stem cells (hDPSCs) have yet to be identified.

Design: Microspectrofluorimetry technique with pH-sensitive fluorescent dye, BCECF, was used to detect pHi changes. NH4Cl and Na+-acetate pre-pulse were used to induce intracellular acidosis and alkalosis, respectively. Isoforms of pHi-regulators were detected by Western blot technique.

Results: The resting pHi was no significant difference between that in HEPES-buffered (nominal HCO3--free) solution or CO2/HCO3-buffered system (7.42 and 7.46, respectively). The pHi recovery following the induced-intracellular acidosis was blocked completely by removing [Na+]o, while only slowed (-63%) by adding HOE694 (a NHE1 specific inhibitor) in HEPES-buffered solution. The pHi recovery was inhibited entirely by removing [Na+]o, while adding HOE 694 pulse DIDS (an anion-transporter inhibitor) only slowed (-55%) the acid extrusion. Both in HEPES-buffered and CO2/HCO3-buffered system solution, the pHi recovery after induced-intracellular alkalosis was entirely blocked by removing [Cl-]o. Western blot analysis showed the isoforms of pHi regulators, including NHE1/2, NBCe1/n1, AE1/2/3/4 and CHE in the hDPSCs.

Conclusions: We demonstrate for the first time that resting pHi is significantly higher than 7.2 and meditates functionally by two Na+-dependent acid extruders (NHE and NBC), two Cl--dependent acid loaders (CHE and AE) and one Na+-independent acid extruder(s) in hDPSCs. These findings provide novel insight for basic and clinical treatment of dentistry.

Keywords: Cl(−)/HCO(3)(−) Exchanger; Cl(−)/OH(−) Exchanger; Fluorescent-BCECF; Human dental pulp stem cells; Na(+)-H(+) Exchanger; Na(+)-HCO(3)(−) Co-transporter.

MeSH terms

  • Acid-Base Equilibrium / physiology*
  • Acid-Base Imbalance
  • Acids / pharmacology
  • Ammonium Chloride
  • Antiporters / metabolism
  • Apoptosis
  • Buffers
  • Cell Differentiation
  • Cell Proliferation
  • Cytoplasm / drug effects
  • Cytoplasm / metabolism*
  • Dental Pulp / metabolism*
  • Guanidines / pharmacology
  • Homeostasis / physiology*
  • Humans
  • Hydrogen-Ion Concentration
  • Ion Pumps / drug effects
  • Ion Pumps / metabolism
  • Neoplasm Metastasis
  • Protein Isoforms
  • Sodium / pharmacology
  • Sodium-Bicarbonate Symporters / metabolism
  • Sodium-Hydrogen Exchanger 1 / metabolism
  • Sodium-Hydrogen Exchangers / metabolism
  • Stem Cells / drug effects
  • Stem Cells / metabolism*
  • Sulfones / pharmacology

Substances

  • Acids
  • Antiporters
  • Buffers
  • Guanidines
  • Ion Pumps
  • Protein Isoforms
  • SLC4A4 protein, human
  • SLC4A7 protein, human
  • SLC9A1 protein, human
  • SLC9A2 protein, human
  • Sodium-Bicarbonate Symporters
  • Sodium-Hydrogen Exchanger 1
  • Sodium-Hydrogen Exchangers
  • Sulfones
  • chloride-base exchanger
  • Ammonium Chloride
  • 3-methylsulfonyl-4-piperidinobenzoyl guanidine
  • Sodium