Glomerular mesangial cells: Electrophysiology and regulation of contraction

James D. Stockand, Steven C. Sansom

Research output: Contribution to journalReview article

159 Citations (Scopus)

Abstract

Mesangial cells are smooth muscle-like pericytes that abut and surround the filtration capillaries within the glomerulus. Studies of the fine ultrastructure of the glomerulus show that the mesangial cell and the capillary basement membrane form a biomechanical unit capable of regulating filtration surface area as well as intraglomerular blood volume. Structural and functional studies suggest that mesangial cells regulate filtration rate in both a static and dynamic fashion. Mesangial excitability enables a homeostatic intraglomerular stretch reflex that integrates an increase in filtration pressure with a reduction in capillary surface area. In addition, mesangial tone is regulated by diverse vasoactive hormones. Agonists, such as angiotensin II, contract mesangial cells through a signal transduction pathway that releases intracellular stores of Ca2+, which subsequently activate nonselective cation channels and C1- channels to depolarize the plasma membrane. The change in membrane potential activates voltage-gated Ca channels, allowing Ca2+ cell entry and further activation of depolarizing conductances. Contraction and entry of cell Ca2+ are inhibited only when Ca2+-activated K+ channels (BE(Ca)) are activated and the membrane is hyperpolarized toward the K+ equilibrium potential. The mesangial BK(Ca) is a weak regulator of contraction in unstimulated cells; however, the gain of the feedback is increased by atrial natriuretic peptide, nitric oxide, and the second messenger cGMP, which activates protein kinase G and decreases both the voltage and Ca2+ activation thresholds of BK(Ca) independent of sensitivity. This enables BK(Ca) to more effectively counter membrane depolarization and voltage-gated Ca2+ influx. After hyperpolarizing the membrane, BK(Ca) rapidly inactivates because of dephosphorylation by protein phosphatase 2A. Regulation of ion channels has been linked casually to hyperfiltration during early stages of diabetes mellitus. Determining the signaling pathways controlling the electrophysiology of glomerular mesangial cells is important for understanding how glomerular filtration rate is regulated in health and disease.

Original languageEnglish (US)
Pages (from-to)723-744
Number of pages22
JournalPhysiological Reviews
Volume78
Issue number3
DOIs
StatePublished - Jul 1998

Fingerprint

Mesangial Cells
Electrophysiology
Membranes
Calcium-Activated Potassium Channels
Cyclic GMP-Dependent Protein Kinases
Protein Phosphatase 2
Stretch Reflex
Pericytes
Atrial Natriuretic Factor
Second Messenger Systems
Contracts
Blood Volume
Glomerular Filtration Rate
Ion Channels
Basement Membrane
Angiotensin II
Membrane Potentials
Smooth Muscle
Cations
Signal Transduction

ASJC Scopus subject areas

  • Physiology
  • Molecular Biology
  • Physiology (medical)

Cite this

Glomerular mesangial cells : Electrophysiology and regulation of contraction. / Stockand, James D.; Sansom, Steven C.

In: Physiological Reviews, Vol. 78, No. 3, 07.1998, p. 723-744.

Research output: Contribution to journalReview article

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