RESUMO
A new four parameter Tang-Toennies type potential model is described for the a 3Σu + triplet state of the alkali dimers Na2, K2, Rb2, and Cs2. Compared to an earlier three parameter semi-empirical model based on the experimental well depth, De, well location, Re, and the harmonic vibrational frequency, ωe [Lau et al., J. Chem. Phys. 145, 194308 (2016)], the new model is also adjusted to be consistent with the scattering length. The results are shown to have a similar good agreement with the spectroscopic term values as the earlier model with the advantage that the scattering length is properly described. The deviations from recent potentials for Cs2 are discussed.
RESUMO
Autoantibodies of the IgG class against N-methyl-d-aspartate-receptor subunit NR1 (NMDAR1) were first described in anti-NMDAR encephalitis and seen as disease indicators. Recent work on together over 5000 individuals challenged this exclusive view by showing age-dependently up to >20% NMDAR1-autoantibody seroprevalence with comparable immunoglobulin class and titer distribution across health and disease. The key question therefore is to understand the properties of these autoantibodies, also in healthy carriers, in order to assess secondary complications and possible contributions to neuropsychiatric disease. Here, we believe we provide for human NMDAR1-autoantibodies the first comprehensive analysis of their target epitopes and functionality. We selected sera of representative carriers, healthy or diagnosed with very diverse conditions, that is, schizophrenia, age-related disorders like hypertension and diabetes, or anti-NMDAR encephalitis. We show that all positive sera investigated, regardless of source (ill or healthy donor) and immunoglobulin class, provoked NMDAR1 internalization in human-induced pluripotent stem cell-derived neurons and reduction of glutamate-evoked currents in NR1-1b/NR2A-expressing Xenopus oocytes. They displayed frequently polyclonal/polyspecific epitope recognition in the extracellular or intracellular NMDAR1 domains and some additionally in NR2A. We conclude that all circulating NMDAR1-autoantibodies have pathogenic potential regarding the whole spectrum of neuronal NMDAR-mediated effects upon access to the brain in situations of increased blood-brain-barrier permeability.
Assuntos
Autoanticorpos/sangue , Epitopos/metabolismo , Imunoglobulina A/metabolismo , Imunoglobulina G/metabolismo , Imunoglobulina M/metabolismo , Receptores de N-Metil-D-Aspartato/imunologia , Idoso , Animais , Endocitose/fisiologia , Feminino , Fibroblastos/imunologia , Ácido Glutâmico/metabolismo , Humanos , Células-Tronco Pluripotentes Induzidas/imunologia , Masculino , Potenciais da Membrana/fisiologia , Transtornos Mentais/sangue , Transtornos Mentais/imunologia , Pessoa de Meia-Idade , Doenças do Sistema Nervoso/sangue , Doenças do Sistema Nervoso/imunologia , Neurônios/imunologia , Oócitos , Xenopus laevisRESUMO
For the past century, fingerprints have been considered permanent and specific for each individual. However, with the advances in transplantology, fingerprints have lost their permanence. Because no study has yet been described, we examined possible changes in the fingerprint pattern of a transplanted hand. In 2006, we performed a hand transplantation on a 32-year-old man. The donor was revealed to have had a criminal record; his fingerprints were stored in the Polish automated fingerprint identification system. A forensic technician fingerprinted the transplanted hand nine times between June 2006 and September 2009. The appearance of minutiae and white lines and the change in the distance between papillary ridges were assessed in the thumbprints of the transplanted hand. The appearance of white lines was only temporary; at no point did they impair fingerprint identification. No significant changes occurred in the distance between the friction ridges. The observed small differences were ascribed to the two techniques used to collect the prints (spoon vs rolling). The number of minutiae ranged from 1 to 3, reaching a maximum in the third posttransplant month. A 40-month observation showed no significant changes in the fingerprints of the transplanted hand. Nevertheless, a long-term study is needed because of the risk of chronic rejection. The noninvasiveness of dactylography argues for inspecting its application to diagnose acute rejection. Finally, lawmakers should be made aware of the personal-protection issues related to the growing number of hand-transplant recipients.