Background Cell therapy is one of the most promising therapeutic interventions for retinitis pigmentosa. In the current study, we aimed to assess if peripheral blood-derived monocytes which are highly abundant and accessible could be utilized as a potential candidate for phenotypic differentiation into neuron-like cells. Methods The peripheral blood-derived monocytes were reconditioned phenotypically using extrinsic growth factors to induce pluripotency and proliferation. The reconditioned monocytes (RM) were further incubated with a cocktail of growth factors involved in retinal development and growth to induce retinal neuron-like properties. These cells, termed as retinal neuron-like cells (RNLCs) were characterized for their morphological, molecular and functional behaviour in vitro and in vivo. Results The monocytes de-differentiated in vitro and acquired pluripotency with the expression of prominent stem cell markers. Treatment of RM with retinal growth factors led to an upregulation of neuronal and retinal lineage markers and downregulation of myeloid markers. These cells show morphological alterations resembling retinal neuron-like cells and expressed photoreceptor (PR) markers. The induced RNLCs also exhibited relative membrane potential change upon light exposure suggesting that they have gained some neuronal characteristics. Further studies showed that RNLCs could also integrate in an immune-deficient retinitis pigmentosa mouse model NOD.SCID-rd1 upon sub-retinal transplantation. The RNLCs engrafted in the inner nuclear layer (INL) and ganglion cell layer (GCL) of the RP afflicted retina. Mice transplanted with RNLCs showed improvement in depth perception, exploratory behaviour and the optokinetic response. Conclusions This proof-of-concept study demonstrates that reconditioned monocytes can be induced to acquire retinal neuron-like properties through differentiation using a defined growth media and can be a potential candidate for cell therapy-based interventions and disease modelling for ocular diseases.

Retinitis pigmentosa (RP) is a common retinal degeneration disease caused by mutation in any gene of the photo transduction cascade and results in photoreceptor dystrophy. Over decades, several animal models have been used to address the need for the elucidation of effective therapeutics and factors regulating retinal degeneration to prohibit or renew the damaged retina. However, controversies over the immune privilege of retina during cell transplantation and the role of immune modulation during RP still remain largely uninvestigated because of the lack of suitable animal models. Here, we have developed an immunocompromised mouse model, NOD.SCID-rd1, for retinitis pigmentosa (RP) by crossing CBA/J and NOD SCID mice and selecting homozygous double mutant animals for further breeding. Characterization of the newly developed RP model indicates a similar retinal degeneration pattern as CBA/J, with a decreased apoptosis rate and rhodopsin loss. It also exhibits loss of T cells, B cells and NK cells. The NOD.SCID-rd1 model is extremely useful for allogenic and xenogenic cell-based therapeutics, as indicated by the higher cell integration capacity post transplantation. We dissect the underlying role of the immune system in the progression of RP and the effect of immune deficiency on immune privilege of the eye using comparative qPCR studies of this model and the immune-competent RP model.

Dear Editor,Soluble cardiac troponin T (cTnT), an indicator of myocardial injury and stress, is used in decision management for patients with cardiovascular disease (CVD). As highly sensitive assays can detect elevated concentrations of cTnT even in healthy individuals (e.g. outside of myocardial necrosis, electrocardiographic changes or angina) and cannot distinguish among disease conditions, 1,2 a comprehensive understanding of the cTnT-secretome is an unmet need.Within the secretome, cTnT is not only present as a soluble factor but may also be contained within extracellular vesicles (EVs). 3 EVs are nanoscale particles secreted by all cells, the cargoes of which can reflect the molecular composition of the cells of origin 4 and indicate disease or injury. 5 As EVs are easily sampled from plasma, 6 they are being developed as a 'liquid' biopsy reflecting the disease state from the tissue of origin. Here, we advanced a fluorescence-based super-resolution microscopy technique, quantitative single-molecule localization microscopy (qSMLM), to robustly characterize cTnT-positive EVs. Importantly, we provide the first report of cTnT-secretome across a spectrum of CVDs.EVs were purified from induced pluripotent stem cellderived cardiomyocyte cell media (CCM), representing a source of cardiomyocyte-derived EVs (Figure S1), and patient plasma (Figures S2): healthy subjects (n = 5), patients with heart failure (HF; n = 5), hypertrophic cardiomyopathy (n = 3), type 1 myocardial infarction (MI-TI, n = 5) or type 2 myocardial infarction (MI-TII; n = 5) and chronic kidney disease (CKD; n = 5). In all cases (Figures S1 and S2), EVs had intact morphology and contained canonical EV markers (tetraspanins CD9, CD63, CD81; luminal marker TSG101) with low amounts of soluble proteins. According to dot blots (Figure S2C), the CD81 content of patient EVs was highly variable, whereas combined tetraspanins had more uniform expression. Table S1 shows patient characteristics. Control patients wereThis is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

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