Linda Sinclair

Linda Sinclair

@lindavsinclair.bsky.social

Immunologist, working with Cantrell Lab. Interested in LOTS - focused on nutrient and metabolic control of the immune system. (opinions are my own)

2.4K followers581 following39 posts

Pinned

Linda Sinclair reposted

Linda Sinclair reposted

Linda Sinclair reposted

Special issue Immunometabolism and Beyond: from Liver to Brain! European Journal of Immunology Article types: reviews and research articles Submission deadline 1 November 2025 Thanks to Nadja, Matteo and Bin for this wonderful opportunity! #immunometabolism #EJI #CRC1292 #CRC355 #CRC156 #FZI

Linda Sinclair reposted

What if Tregs are not a separate lineage, but part of spontaneously activated T cells? In this work, we integrate this idea with our recent findings: Adult T cell leukemia (ATL) is not 'Treg cancer', challenging the current concept of Treg as a distinct entity.🧵(1/4) academic.oup.com/discovimmuno...

academic.oup.comSpectrum of Treg and self-reactive T cells: single cell perspectives from old friend HTLV-1Summary. Despite extensive regulatory T cell (Treg) research, fundamental questions on in vivo dynamics remain to be answered. The current study aims to di

Linda Sinclair reposted

Very excited to be just a weekend away from this UK conference on neutrophil biology that we are hosting at Newcastle. It includes international keynotes but most important the majority of speakers are early career researchers. #immunology #inflammation #neutrophils #humandisease

Linda Sinclair reposted

Two weeks left to apply for a postdoc position with the Slack group! Please spread the word!

Emma Slack@mucosalimmunology.bsky.social

Interested in microbial #metabolism, #mucosalbiology and #UTI? Then check out the open postdoctoral position in the Mucosal Immunology Group at ETH Zurich! NB: All applications must go via the ETH job portal: www.jobs.ethz.ch/job/view/JOP... Closing date: 24th Feburary 🧪🧫🔬

Linda Sinclair reposted

I'm very pleased to have two lab positions open this week, to join our team looking at immune regulation in infection and co-infection. We're especially interested in tissue-based immunity, cytokine regulation and immune metabolism. Join us! Postdoc (3y) and research technician (12mo) posts open.

Linda Sinclair reposted

Linda Sinclair reposted

Okey dokey here goes! First real post - please reshare if appropriate 🙏 🔔We’ve got two postdoc level positions opening in our lab! One wet lab, one computational🔔 We’re a scientifically diverse, friendly bunch working at the interface of mitochondrial biology, metabolism & cancer in Glasgow, UK.

4/n So, we used Ian Ganley's autophagy flux reporter (mCherry-GFP:LC3b) mouse: Flux can be measured by comparing the level of GFP (quenched in autolysosome) to mCherry (stable) fluorescence. *Naïve CD8 Tcells have very autophagy flux, which is REDUCED in response to TCR activation*

11/n Proteomics on naïve CD8 Tcells +/- VPS34 inhibition showed the predominant substrates are mitochondrial proteins. In naïve CD8 T cells mitochondria are constantly pruned to remain healthy. Blocking autophagy results in accumulation of pro-apoptotic proteins eg BAK1 and BIM, and cell death.

9/n “protected proteins” (autophagy targets) include cytolytic effectors; amino acid, glucose and lactate transporters; as well as proteins involved in metabolism (FAO, amino acid metabolism, and glycolysis)

10/n Proteins which are fuelled by autophagy during AA starvation include “protective” proteins eg cell detoxification and survival. *keeping autophagy REPRESSED in effector CD8 cells permits cytolytic and metabolic processes; whilst AA starvation drives autophagy fuelled cell survival proteins*

7/n Does extracellular AA supply/accessibility control autophagy in CD8 Tcells? Yes, autophagy repression in CD8 Tcells was dynamic, and dependent upon extracellular AA availability. In effector CD8 Tcells, this was through VPS34-dependent, but AMPK/mTORC1-independent pathways.

8/n What are the substrates of autophagy in CD8 Tcells? They are different in naïve cells and effector cells! - Proteomics on CTLs showed AA deprivation drives a loss in 55% of proteins ~ ½ of this loss was protected by VPS34 inhibition=autophagy. ½ was not (ie degraded by other mechanisms).

5/n What immune signals are regulating autophagy flux? As well as TCR-activation, Pro-inflammatory cytokines (IL-2, IL-12+IL-18, IL-4, IL-21) repressed autophagy flux; but memory cytokines (IL-15, IL-7) could not.

6/n We saw that autophagy repression correlated with the amino acid (AA) uptake capacity of the cells. ~AA starvation is an evolutionarily conserved autophagy stimulus. ~AA transporter expression is tightly regulated in Tcells: LOW in naïve, HIGH in effector cells and LOW in memory cells.

2/n The basis and framework for this behemoth study was all grown from Tom's PhD work. Tom noted protein and RNA expression of key autophagy machinery/cargo adaptors showed a disconnect during activation and differentiation of CD8 T cells. Protein INCREASED while mRNA DECREASED. What was going on?

3/n Autophagy is a degradation pathway. Is the increased protein expression of autophagy “core components” indicative of REDUCED autophagy flux post activation? (rather than increased in autophagy after immune activation, as currently understood)

Linda Sinclair reposted

Linda Sinclair reposted

Michael J Fox has had tremendous influence on people with Parkinson's Disease (PD), their carers, families and those working on PD. He is a shining example of what a single person is capable of. Well deserved recognition.

WuTangIsForTheChildren@wutangforchildren.bsky.social

Michael J. Fox receiving the Presidential Medal of Freedom from Joe Biden….why is it so dusty in here now….I’m not crying, you’re crying 🥹🙏

Linda Sinclair reposted

Organelles meets dinos! 🦖🔬 Featuring Mitosaur, ERsaur, Golgisaur, Lysosaur, and others, it's such a creative take on the cellular world we know and love. 💚 Which dino-organelle is your favorite? Let us know below! 👇

Linda Sinclair reposted

T cells get hungry! Check out Shixin Ma's new paper showing nutrient switching controls T cell exhaustion. Nutrients metabolized in the nucleus by ACSS2 and ACLY direct histone acetylation at key loci via binding to specific HATs, indicating a metabolic code guides our histone code. @science.org

Linda Sinclair reposted