Citation

  • Authors: Li, N., Mruk, D. D., Tang, E. I., Lee, W. M., Wong, C. K., Cheng, C. Y.
  • Year: 2016
  • Journal: Endocrinology 157 2894-908
  • Applications: in vivo / siRNA / in vivo-jetPEI

Method

0.16 nmol (2µg) of siRNA was delivered with in vivo-jetPEI at a N/P ratio of 6 (0.32µl) through intratesticular injection to rat testis.

Abstract

Formin 1 confers actin nucleation by generating long stretches of actin microfilaments to support cell movement, cell shape, and intracellular protein trafficking. Formin 1 is likely involved in microtubule (MT) dynamics due to the presence of a MT binding domain near its N terminus. Here, formin 1 was shown to structurally interact with alpha-tubulin, the building block of MT, and also end-binding protein 1 (a MT plus [+]-end-binding protein that stabilizes MT) in the testis. Knockdown of formin 1 in Sertoli cells with an established tight junction barrier was found to induce down-regulation of detyrosinated MT (a stabilized form of MT), and disorganization of MTs, in which MTs were retracted from the cell cortical zone, mediated through a loss of MT polymerization and down-regulation of Akt1/2 signaling kinase. An efficient knockdown of formin 1 in the testis reduced the number of track-like structures conferred by MTs and F-actin considerably, causing defects in spermatid and phagosome transport across the seminiferous epithelium. In summary, formin1 maintains MT and F-actin track-like structures to support spermatid and phagosome transport across the seminiferous epithelium during spermatogenesis.

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