Plasma cells, the terminal effectors of the B lymphoid lineage, are responsible for the humoral arm of adaptive immunity. Their differentiation from B cells entails a profound cellular reshaping inherently associated with stress. Autophagy is a conserved adaptive cellular strategy recently implicated in differentiation and immunity. We identified a novel autophagic function in plasma cells. Autophagy restricts the expression of the transcriptional repressor Blimp-1 and immunoglobulins through a selective negative control on the endoplasmic reticulum and its stress signaling response, thereby optimizing energy and viability. As a result, autophagy in vivo sustains antibody responses, and is an essential intrinsic determinant of the bone marrow long-lived plasma cell niche. Here, I discuss several immune and biomedical implications, and experimental issues to be addressed in the near future. (C) 2014 Published by Elsevier Ltd.

Autophagy, a new determinant of plasma cell differentiation and antibody responses / Cenci, S. - In: MOLECULAR IMMUNOLOGY. - ISSN 0161-5890. - 62:2(2014), pp. 289-295. [10.1016/j.molimm.2014.02.008]

Autophagy, a new determinant of plasma cell differentiation and antibody responses

Cenci S
Primo
2014-01-01

Abstract

Plasma cells, the terminal effectors of the B lymphoid lineage, are responsible for the humoral arm of adaptive immunity. Their differentiation from B cells entails a profound cellular reshaping inherently associated with stress. Autophagy is a conserved adaptive cellular strategy recently implicated in differentiation and immunity. We identified a novel autophagic function in plasma cells. Autophagy restricts the expression of the transcriptional repressor Blimp-1 and immunoglobulins through a selective negative control on the endoplasmic reticulum and its stress signaling response, thereby optimizing energy and viability. As a result, autophagy in vivo sustains antibody responses, and is an essential intrinsic determinant of the bone marrow long-lived plasma cell niche. Here, I discuss several immune and biomedical implications, and experimental issues to be addressed in the near future. (C) 2014 Published by Elsevier Ltd.
2014
Antibody; Atg5; Autophagy; B cell; Blimp-1; Endoplasmic reticulum; ER-phagy; Immunological memory; Multiple myeloma; Plasma cell; Proteostasis; Reticulophagy; Ubiquitin; Unfolded protein response; XBP-1
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/146496
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