T Cells from NOD-PerIg Mice Target Both Pancreatic and Neuronal Tissue.
Jeremy J RacineHarold D ChapmanRosalinda DotyBrynn M CairnsTimothy J HinesAbigail L D TadenevLaura C AndersonTorrian GreenMeaghan E DyerJanine M WottonZoë BichlerJacqueline K WhiteRachel EttingerRobert W BurgessDavid V SerrezePublished in: Journal of immunology (Baltimore, Md. : 1950) (2020)
It has become increasingly appreciated that autoimmune responses against neuronal components play an important role in type 1 diabetes (T1D) pathogenesis. In fact, a large proportion of islet-infiltrating B lymphocytes in the NOD mouse model of T1D produce Abs directed against the neuronal type III intermediate filament protein peripherin. NOD-PerIg mice are a previously developed BCR-transgenic model in which virtually all B lymphocytes express the H and L chain Ig molecules from the intra-islet-derived anti-peripherin-reactive hybridoma H280. NOD-PerIg mice have accelerated T1D development, and PerIg B lymphocytes actively proliferate within islets and expand cognitively interactive pathogenic T cells from a pool of naive precursors. We now report adoptively transferred T cells or whole splenocytes from NOD-PerIg mice expectedly induce T1D in NOD.scid recipients but, depending on the kinetics of disease development, can also elicit a peripheral neuritis (with secondary myositis). This neuritis was predominantly composed of CD4+ and CD8+ T cells. Ab depletion studies showed neuritis still developed in the absence of NOD-PerIg CD8+ T cells but required CD4+ T cells. Surprisingly, sciatic nerve-infiltrating CD4+ cells had an expansion of IFN-γ- and TNF-α- double-negative cells compared with those within both islets and spleen. Nerve and islet-infiltrating CD4+ T cells also differed by expression patterns of CD95, PD-1, and Tim-3. Further studies found transitory early B lymphocyte depletion delayed T1D onset in a portion of NOD-PerIg mice, allowing them to survive long enough to develop neuritis outside of the transfer setting. Together, this study presents a new model of peripherin-reactive B lymphocyte-dependent autoimmune neuritis.
Keyphrases
- high fat diet induced
- type diabetes
- innate immune
- peripheral blood
- induced apoptosis
- mouse model
- insulin resistance
- multiple sclerosis
- cell cycle arrest
- poor prognosis
- wild type
- cardiovascular disease
- rheumatoid arthritis
- immune response
- type iii
- adipose tissue
- cell proliferation
- cerebral ischemia
- metabolic syndrome
- skeletal muscle
- cognitive decline
- nk cells
- subarachnoid hemorrhage
- interstitial lung disease
- brain injury
- endoplasmic reticulum stress
- blood brain barrier