Skip to main content
. 2014 Dec 29;2(2):021006. doi: 10.1117/1.NPh.2.2.021006

Fig. 4.

Fig. 4

Thinner branches experience greater AP-Ca2+ amplitudes. (a) A layer 5 pyramidal cell filled with OGB1, AF594, and biocytin was reconstructed after the calcium imaging session. (b) Upper: two dendrites (black) were in the same focal plane allowing simultaneous recordings. Lower: 100× magnification lens used to measure dendritic diameters. (c) Current injections into the soma were used to initiate three APs with interspike interval of 20 ms. Simultaneous recordings of dendritic AP-Ca2+ signals at two locations marked in (b). (d) Diameters of sister branches in each pair were normalized against the branch with greater diameter (x axis). AP-Ca2+ signal amplitudes were normalized against the stronger branch in a pair (y axis). Sister branch pairs are connected by straight lines. Note that AP-Ca2+ signal amplitudes were regularly greater in thinner branches. (e1) Each dendritic pair (N=15) is represented by three values: (i) diameter of thinner branch divided by diameter of thicker branch (dotted bar), (ii) calculated surface-to-volume ratio (SVR) of thinner branch divided by calculated SVR of thicker branch (light gray bar), and (iii) measured Ca2+ signal in thinner branch divided by Ca2+ signal in thicker branch (dark gray bar). Note that in sister branches with similar dendritic diameters (diameter ratio=1), as determined in dendritic pair #9 or dendritic pair #10, the AP-induced Ca2+ transients were very similar, too (Ca2+ Ratio=1). (e2) The measured value (Ca2+_thin/Ca2+_thick) is plotted against the predicted value (SVR_thin/SVR_thick) for each dendritic pair (N=15). Linear regression (forced through zero) has a negative R2.