Fluorescence imaging of individual bullfrog saccular stereocilia quantifies free [Ca2+] dynamics under MET-channel gating. Four mechanisms collectively account for observed Ca2+ clearance: free diffusion, PMCA pumping, fixed buffer binding, and mobile buffer binding. This is the primary source for apical compartment geometry and resting [Ca2+] used in h05 ODE models.

Key finding

Resting free [Ca2+] in bullfrog saccular stereocilia is 20–310 nM depending on condition (Figure 9A reports ~0.31 µM at saturating deflection; baseline is lower). The stereociliary compartment is geometrically small (~0.05 pL = 50 fL for a single stereocilium), justifying the lumped V_apex parameter. All four Ca2+ regulatory mechanisms are required: no single mechanism accounts for observed clearance kinetics.

Numbers that matter

ParameterValueUnitsConditionsNotes
Resting free [Ca2+] (bullfrog)20–310nMSaccular stereocilia, fluorescence imaging~0.31 µM at saturating deflection; baseline ~60 nM
Single stereocilium volume~50fL (0.05 pL)Estimate from geometry (0.5 µm diameter × ~3 µm)Not directly stated; derivable from geometric parameters in paper
Ca2+ clearance time constant10–100msShort vs. prolonged stimuliFaster component from PMCA + diffusion
PMCA involvementconfirmed essentialVanadate/carboxyeosin block raises Ca2+Quantitative pump rate not given; see Yamoah 1998

Species caveat: Bullfrog (Rana catesbeiana) sacculus. OHC values may differ. Ca2+ fraction parameters require mammalian cross-referencing.

Limitations

  • Bullfrog sacculus, not mammalian OHC. The model transfers qualitatively but resting [Ca2+] in OHC stereocilia may be different.
  • Compartment volume estimated from geometry, not directly measured.
  • Does not report absolute PMCA pump rate; only establishes pump necessity.

Connections