Schake, L. | Search bioRxiv

bioRxiv2024

Non-invasive visualization of pH changes within the tumor-micro-environment by positron emission tomography

Slight changes in the pH value of the tumor microenvironment (TME) have crucial effects on host defense, metastatic behavior, immune regulation and cellular metabolism. Due to the high metabolic activity and insufficient perfusion of tumors, acidic metabolites often accumulate in tumors and can influence the pH of the TME. Several studies have shown that the acidity of the interstitial space and the relatively stable intracellular pH can influence the functions of cancer and stromal cells and their interaction with the extracellular matrix. We describe radiopharmaceutical probes for positron emission tomography (PET) that exploits the increasingly used concept of pH-dependent intratumorally cleavage of PET-tracer to release functional moieties. The radiopharmaceuticals are based on [18F]FDG, a PET tracer, routinely used, and substituents that are pH-dependently cleaved. Utilizing preclinical models, we were able to visualize small pH differences in the acidic TME of different tumors with [18F]FDG-4-methoxybenzylamine ([18F]FDG-4MBA). In vivo studies were in line with in vitro results and showed that the hemiaminal bond between FDG and a substitute is cleaved at slightly acidic pH and leads to pH dependent radiotracer uptake. In vivo neutralization of the acidic extracellular tumor pH by sodium bicarbonate treatment prevents pH-dependent cleavage of [18F]FDG-4MBA and a resulting decrease of uptake. The determination of pH differences in acidic TME may serve as a novel marker for various questions such as regulation of the response to immunotherapies. Notably, even small pH differences in the acidic TME of different tumors, in the same in vivo model, could be visualized. This is the first preclinical study to show that it is possible to visualize small pH differences in the TME of different tumors in the same mouse using hemiaminal bound [18F]FDG. Due to the facile tracer synthesis and application, this system could be well suited for translation into clinical studies to develop new strategies of pH regulation to improve the efficacy of immunotherapy in cancer patients. graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=113 SRC="FIGDIR/small/624628v1_ufig1.gif" ALT="Figure 1"> View larger version (32K): org.highwire.dtl.DTLVardef@1c338c8org.highwire.dtl.DTLVardef@1c4fc67org.highwire.dtl.DTLVardef@197036aorg.highwire.dtl.DTLVardef@1613fa2_HPS_FORMAT_FIGEXP M_FIG C_FIG

cancer biology↗

bioRxiv2021

Complexome profiling on the lpa2 mutant reveals insights into PSII biogenesis and new PSII associated proteins

We have identified the homolog of LOW PSII ACCUMULATION 2 (LPA2) in Chlamydomonas. A Chlamydomonas lpa2 mutant grew slower in low light and was hypersensitive to high light. PSII maximum quantum efficiency was reduced by 38%. Synthesis and stability of newly made PSII core subunits D1, D2, CP43, and CP47 were not impaired. Complexome profiling revealed that in the mutant CP43 was reduced to [~]23%, D1, D2, and CP47 to [~]30% of wild-type levels, while small PSII core subunits and components of the oxygen evolving complex were reduced at most by factor two. PSII supercomplexes, dimers, and monomers were reduced to 7%, 26%, and 60% of wild-type levels, while RC47 was increased [~]6-fold. Our data indicate that LPA2 acts at a step during PSII assembly without which PSII monomers and especially further assemblies become intrinsically unstable and prone to degradation. Levels of ATP synthase and LHCII were 29% and 27% higher in the mutant than in the wild type, whereas levels of the cytochrome b6f complex were unaltered. While the abundance of PSI core subunits and antennae hardly changed, LHCI antennae were more disconnected in the lpa2 mutant, presumably as an adaptive response to reduce excitation of PSI. The disconnection of LHCA2,9 together with PSAH and PSAG was the prime response, but independent and additional disconnection of LHCA1,3-8 along with PSAK occurred as well. Finally, based on co-migration profiles, we identified three novel putative PSII associated proteins with potential roles in regulating PSII complex dynamics, assembly, and chlorophyll breakdown. One-sentence summaryWe provide evidence that the Chlamydomonas LPA2 homolog acts at a step in PSII biogenesis without which PSII monomers and further assemblies become unstable and prone to degradation.

plant biology↗