Bio

Institute Affiliations


  • Member, Maternal & Child Health Research Institute (MCHRI)

Publications

All Publications


  • Hydrogel-based delivery of Il-10 improves treatment of bleomycin-induced lung fibrosis in mice. Biomaterials Shamskhou, E. A., Kratochvil, M. J., Orcholski, M. E., Nagy, N., Kaber, G., Steen, E., Balaji, S., Yuan, K., Keswani, S., Danielson, B., Gao, M., Medina, C., Nathan, A., Chakraborty, A., Bollyky, P. L., De Jesus Perez, V. A. 2019; 203: 52?62

    Abstract

    Idiopathic pulmonary fibrosis (IPF) is a life-threatening progressive lung disorder with limited therapeutic options. While interleukin-10 (IL-10) is a potent anti-inflammatory and anti-fibrotic cytokine, its utility in treating lung fibrosis has been limited by its short half-life. We describe an innovative hydrogel-based approach to deliver recombinant IL-10 to the lung for the prevention and reversal of pulmonary fibrosis in a mouse model of bleomycin-induced lung injury. Our studies show that a hyaluronan and heparin-based hydrogel system locally delivers IL-10 by capitalizing on the ability of heparin to reversibly bind IL-10 without bleeding or other complications. This formulation is significantly more effective than soluble IL-10 for both preventing and reducing collagen deposition in the lung parenchyma after 7 days of intratracheal administration. The anti-fibrotic effect of IL-10 in this system is dependent on suppression of TGF-? driven collagen production by lung fibroblasts and myofibroblasts. We conclude that hydrogel-based delivery of IL-10 to the lung is a promising therapy for fibrotic lung disorders.

    View details for PubMedID 30852423

  • Angiopoietin like-4 as a novel vascular mediator in capillary cerebral amyloid angiopathy BRAIN Chakraborty, A., Kamermans, A., van het Hof, B., Castricum, K., Aanhane, E., van Horssen, J., Thijssen, V. L., Scheltens, P., Teunissen, C. E., Fontijn, R. D., van der Flier, W. M., de Vries, H. E. 2018; 141: 3377?88

    Abstract

    Increasing evidence suggests that vascular dysfunction in the brain is associated with early stages of Alzheimer's disease. Amyloid-? deposition in the microvasculature of the brain, a process referred to as capillary cerebral amyloid angiopathy (capillary CAA), propagates vascular remodelling, which results in impaired function of the blood-brain barrier, reduced cerebral perfusion and increased hypoxia. While improving vascular function may be an attractive new way to fight capillary CAA, the underlying factors that mediate vascular alterations in Alzheimer's disease and capillary CAA pathogenesis remain largely unknown. Here we provide first evidence that angiopoietin like-4 (ANGPTL4), a hypoxia-induced factor, is highly expressed by reactive astrocytes in well characterized post-mortem tissues of patients with capillary CAA. Our in vitro studies reveal that ANGPTL4 is upregulated and secreted by human cortical astrocytes under hypoxic conditions and in turn stimulates endothelial cell migration and sprouting in a 3D spheroid model of human brain endothelial cells. Interestingly, plasma levels of ANGPTL4 are significantly increased in patients with vascular dementia compared to patients with subjective memory complaints. Overall, our data suggest that ANGPTL4 contributes to pathological vascular remodelling in capillary CAA and that detection of ANGPTL4 levels may improve current diagnostics. Ways of counteracting the detrimental effects of ANGPTL4 and thus promoting cerebral vascular function may provide novel treatment regimens to halt the progression of Alzheimer's disease.

    View details for DOI 10.1093/brain/awy274

    View details for Web of Science ID 000456597100014

    View details for PubMedID 30462206

  • Vascular Endothelial Growth Factor remains unchanged in cerebrospinal fluid of patients with Alzheimer's disease and vascular dementia ALZHEIMERS RESEARCH & THERAPY Chakraborty, A., Chatterjee, M., Twaalfhoven, H., Milan, M., Teunissen, C. E., Scheltens, P., Fontijn, R. D., van Der Flier, W. M., de Vries, H. E. 2018; 10: 58

    Abstract

    Increasing evidence suggests that cerebral vascular dysfunction is associated with the early stages of Alzheimer's disease (AD). Vascular endothelial growth factor (VEGF) is one of the key players involved in the development and maintenance of the vasculature. Here, we hypothesized that VEGF levels in cerebrospinal fluid (CSF) may be altered in AD patients with vascular involvement, characterized by the presence of microbleeds (MB), and in vascular dementia (VaD) patients compared to controls.VEGF levels were determined by electrochemilumiscence Meso Scale Discovery (MULTI-SPOT Assay System) in CSF from age-matched groups of controls with subjective cognitive decline (n?=?21), AD without MB (n?=?25), AD with MB (n?=?25), and VaD (n?=?21) patients.The average level of VEGF in the different groups was 2.8?±?1 pg/ml CSF. Adjusted for age and gender, no significant differences were detected between groups (p?>?0.5). However, we detected a significant correlation between the concentration of VEGF in the CSF and age (r?=?0.22, p?=?0.03). In addition, males (n?=?54) revealed higher VEGF levels in their CSF compared to females (n?=?38) (males?=?3.08?±?0.769 pg/ml (mean?±?SD), females?=?2.6?±?0.59; p?=?0.006), indicating a gender-related regulation.Our study suggests that VEGF levels in the CSF do not reflect the cerebral vascular alterations in either AD or VaD patients. The observed associations of VEGF with age and gender may indicate that VEGF reflects normal aging and that males and females may differ in their aging process.

    View details for DOI 10.1186/s13195-018-0385-8

    View details for Web of Science ID 000435911700001

    View details for PubMedID 29933741

    View details for PubMedCentralID PMC6015445

  • The blood brain barrier in Alzheimer's disease VASCULAR PHARMACOLOGY Chakraborty, A., de Wit, N. M., van der Flier, W. M., de Vries, H. E. 2017; 89: 12?18

    Abstract

    Alzheimer's disease (AD) is the most common form of dementia, affecting millions of people worldwide. One of the prominent causative factors of AD pathogenesis is cerebral vascular dysfunction, which results in diminished cerebral perfusion. Moreover, due to the loss of the protective function of the blood-brain barrier (BBB), impaired clearance of excess neurotoxic amyloid beta (A?) occurs, causing vascular perturbation and diminished cognitive functioning. The relationship between the prevalence of AD and vascular risk factors is complex and not fully understood. In this review we illustrate the vascular risk factors, their effects on BBB function and their contributions to the onset of AD. Additionally, we discuss the underlying factors that may lead to altered neurovascular function and/or cerebral hypoperfusion in AD.

    View details for DOI 10.1016/j.vph.2016.11.008

    View details for Web of Science ID 000394922100002

    View details for PubMedID 27894893

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