Table 2.

All INs were morphologically identified

Experiment	BC (n)	MC (n)
Rectification, pairs	14	10
Rectification, NPEC‐AMPA uncaging, with spermine	11	10
Rectification, NPEC‐AMPA uncaging, no spermine	8	NA
Naspm wash‐in, pairs	6	NA
Naspm wash‐in, pairs (control)	6	NA
Naspm wash‐in, NPEC‐AMPA uncaging	7	7
Naspm wash‐in, NPEC‐AMPA uncaging (control)	7	3
NBQX wash‐in, NPEC‐AMPA uncaging	2	2
Rectification of mEPSCs, no spermine	9	NA
Rectification of mEPSCs, with spermine	12	NA
Naspm wash‐in, mEPSCs	5	NA
Naspm wash‐in, mEPSCs (control)	3	NA
Dynamic clamp	5	NA
Total	95	32

Morphologies in Fig. 2 were obtained from 89 BCs and 32 MCs, which constitutes the entire IN data set of the present study. Paired recordings in Fig. 5 included data from two triplet recordings, for which two PCs were connected to the same postsynaptic BC. Additionally, four PC‐BC connections used in rectification measurement (Fig. 5D and E) also served as stability controls for Naspm wash‐in experiments (Fig. 5G and H). Together, this results in a total of 95 experiments in BCs, even though the total number of reconstructed BC morphologies is 89. NA, not available.