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. 2016 Mar 31;310(11):G1015–G1027. doi: 10.1152/ajpgi.00349.2015

Table 1.

SFK role in some physiological and pathophysiological functions in rat pancreatic acini

Variable Yes No
Signaling cascade activation
    Stimulated by 100 nM CCKa SFK, p42/44, JNK
    Basal inhibition by PP2a SFK p42/44, JNK
    PP2 inhibition of CCK-induced stimulationa SFK, p42/44, JNK
Transcription factor activation
    100 nM CCK inducedb STAT3, NF-κB, and AP-1
    PP2 inhibition of basalb STAT3, NF-κB, AP-1
    PP2 inhibition of CCK inducedb STAT3, NF-κB, and AP-1
Chemokine release
    Stimulated by 100 nM CCKc,d MCP-1, MIP-1α, RANTES MIP-2.
    Basal inhibition by PP2c,d MIP-1, MCP-1 MIP-1-α, RANTES
    PP2 inhibition of CCK-induced stimulationc,d MCP-1, MIP-1α, RANTES MIP-2
LDH release
    100 nM CCK inducede Stimulation of 237 ± 32% over control
    PP2 inhibition of basale No effect vs. control
    PP2 inhibition of CCK inducede −59 ± 7%Δ of CCK alone
Cell death caspases activity
    100 nM CCKf Caspase-3, -8, and -9
    PP2 stimulation of basalf Caspase-3, -8, and -9
    PP2 inhibition of CCK-induced LDH releasef Caspase-3, -8, and -9
Trypsinogen activationg Stimulated by 100 nM CCK Not inhibited by PP2
Amylase releaseh Stimulated by CCK at 0.01, 0.1, and 100 nM Not inhibited by PP2 at any concentration

SFK, Src family of kinases; JNK, c-Jun-NH2-terminal kinase; CCK, COOH-terminal octapeptide of cholecystokinin; PP2, 4-amino-5-(4-chlorophenyl)-7-(t-butyl)pyrazolo[3,4-d]pyrimidine; STAT3, signal transducer and activator of transcription-3; AP-1, activator protein-1; MCP-1, monocyte chemotactic protein-1; MIP, macrophage inflammatory protein; RANTES, regulated on activation, normal T cell expressed and secreted.

a

Results are calculated from the data shown in Fig. 1.

b

Concentration and incubation times are reported in Fig. 2.

c

Concentration and incubation times are reported in Fig. 3.

d

Concentration and incubation times are reported in Fig. 4.

e

Concentration and incubation times are reported in Fig. 5.

f

Concentration and incubation times are reported in Fig. 6.

g

Concentration and incubation times are reported in Fig. 7.

h

Concentration and incubation times are reported in Tables 2 and 3.