4.5 Article

Noncanonical Activin A Signaling in PC12 Cells: A Self-Limiting Feedback Loop

期刊

NEUROCHEMICAL RESEARCH
卷 41, 期 5, 页码 1073-1084

出版社

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11064-015-1797-5

关键词

Activin A; Signaling loop; Smad anchor for receptor activation

资金

  1. National Natural Science Foundation [81371298]
  2. Natural Science Fund of Jilin Province [20120723, 2013C030-4]
  3. Frontier Interdiscipline Program of Norman Bethune Health Science Center of Jilin University [2013107028]
  4. Norman Bethune Health Science Center of Jilin University [2013207052]
  5. Jilin University [2015016]

向作者/读者索取更多资源

Activin A (Act A), a member of transforming growth factor-beta superfamily, plays a neuroprotective role in multiple neurological diseases through Act A/Smads signal activation. Traditionally, the up-regulation of Act A gene and extracellular Act A accumulation show the signal activation as a linear pathway. However, one of our discoveries indicated that Act A could lead a loop signaling in ischemic injury. To clarify the characteristic of this loop signaling in a non-pathological state, we up-regulated the expression of Act A, monitored extracellular Act A accumulation and examined the activity of Act A signaling, which was quantified by the expression of phosphorylated Smad3 and the fluorescence intensity of Smad4 in nuclei. The results demonstrated a noncanonical Act A signal loop with self-amplifying property in PC12 cells. Further, it showed self-limiting behavior due to temporary activation and spontaneous attenuation. This periodic behavior of Act A signal loop was found to be regulated by the level of Smad anchor for receptor activation (SARA). Moreover, increased activity of Act A signal loop could promote PC12 cell proliferation and enhance the survival rate of cells to Oxygen-Glucose Deprivation. These practical discoveries will bring new insight on the functional outcome of Act A signaling in neurological diseases by the further understanding: loop signaling.

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