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Abstract
Recent focus on autophagy research has led to new insights on the involvement of ubiquitin (Ub)–mediated signaling as a selectivity factor in autophagy, which is generally considered a nonselective global degradation system. Emerging reports have demonstrated active crosstalk between the Ub-dependent proteolytic system and autophagy. This article highlights recent reports describing Ub-mediated selective autophagy regulated by the Toll-like receptor 4–induced immune response.
