Rejuvenation of three germ layers tissues by exchanging old blood plasma with saline-albumin.


Journal

Aging
ISSN: 1945-4589
Titre abrégé: Aging (Albany NY)
Pays: United States
ID NLM: 101508617

Informations de publication

Date de publication:
30 05 2020
Historique:
received: 13 05 2020
accepted: 20 05 2020
pubmed: 1 6 2020
medline: 3 8 2021
entrez: 1 6 2020
Statut: ppublish

Résumé

Heterochronic blood sharing rejuvenates old tissues, and most of the studies on how this works focus on young plasma, its fractions, and a few youthful systemic candidates. However, it was not formally established that young blood is necessary for this multi-tissue rejuvenation. Here, using our recently developed small animal blood exchange process, we replaced half of the plasma in mice with saline containing 5% albumin (terming it a "neutral" age blood exchange, NBE) thus diluting the plasma factors and replenishing the albumin that would be diminished if only saline was used. Our data demonstrate that a single NBE suffices to meet or exceed the rejuvenative effects of enhancing muscle repair, reducing liver adiposity and fibrosis, and increasing hippocampal neurogenesis in old mice, all the key outcomes seen after blood heterochronicity. Comparative proteomic analysis on serum from NBE, and from a similar human clinical procedure of therapeutic plasma exchange (TPE), revealed a molecular re-setting of the systemic signaling milieu, interestingly, elevating the levels of some proteins, which broadly coordinate tissue maintenance and repair and promote immune responses. Moreover, a single TPE yielded functional blood rejuvenation, abrogating the typical old serum inhibition of progenitor cell proliferation. Ectopically added albumin does not seem to be the sole determinant of such rejuvenation, and levels of albumin do not decrease with age nor are increased by NBE/TPE. A model of action (supported by a large body of published data) is that significant dilution of autoregulatory proteins that crosstalk to multiple signaling pathways (with their own feedback loops) would, through changes in gene expression, have long-lasting molecular and functional effects that are consistent with our observations. This work improves our understanding of the systemic paradigms of multi-tissue rejuvenation and suggest a novel and immediate use of the FDA approved TPE for improving the health and resilience of older people.

Identifiants

pubmed: 32474458
pii: 103418
doi: 10.18632/aging.103418
pmc: PMC7288913
doi:

Substances chimiques

Albumins 0
Saline Solution 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

8790-8819

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL139605
Pays : United States
Organisme : NIA NIH HHS
ID : R56 AG058819
Pays : United States
Organisme : NIBIB NIH HHS
ID : R01 EB023776
Pays : United States

Commentaires et corrections

Type : CommentIn

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Auteurs

Melod Mehdipour (M)

Department of Bioengineering and QB3, UC Berkeley, Berkeley, CA 94720, UDS.

Colin Skinner (C)

Department of Bioengineering and QB3, UC Berkeley, Berkeley, CA 94720, UDS.

Nathan Wong (N)

Department of Bioengineering and QB3, UC Berkeley, Berkeley, CA 94720, UDS.

Michael Lieb (M)

Department of Bioengineering and QB3, UC Berkeley, Berkeley, CA 94720, UDS.

Chao Liu (C)

Department of Bioengineering and QB3, UC Berkeley, Berkeley, CA 94720, UDS.

Jessy Etienne (J)

Department of Bioengineering and QB3, UC Berkeley, Berkeley, CA 94720, UDS.

Cameron Kato (C)

Department of Bioengineering and QB3, UC Berkeley, Berkeley, CA 94720, UDS.

Dobri Kiprov (D)

California Pacific Medical Center, Apheresis Care Group, San-Francisco, CA 94115, USA.

Michael J Conboy (MJ)

Department of Bioengineering and QB3, UC Berkeley, Berkeley, CA 94720, UDS.

Irina M Conboy (IM)

Department of Bioengineering and QB3, UC Berkeley, Berkeley, CA 94720, UDS.

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