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- Callaway, EM, et al.
(författare)
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A multimodal cell census and atlas of the mammalian primary motor cortex
- 2021
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Ingår i: Nature. - : Springer Science and Business Media LLC. - 1476-4687 .- 0028-0836. ; 598:7879, s. 86-102
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Tidskriftsartikel (refereegranskat)abstract
- Here we report the generation of a multimodal cell census and atlas of the mammalian primary motor cortex as the initial product of the BRAIN Initiative Cell Census Network (BICCN). This was achieved by coordinated large-scale analyses of single-cell transcriptomes, chromatin accessibility, DNA methylomes, spatially resolved single-cell transcriptomes, morphological and electrophysiological properties and cellular resolution input–output mapping, integrated through cross-modal computational analysis. Our results advance the collective knowledge and understanding of brain cell-type organization1–5. First, our study reveals a unified molecular genetic landscape of cortical cell types that integrates their transcriptome, open chromatin and DNA methylation maps. Second, cross-species analysis achieves a consensus taxonomy of transcriptomic types and their hierarchical organization that is conserved from mouse to marmoset and human. Third, in situ single-cell transcriptomics provides a spatially resolved cell-type atlas of the motor cortex. Fourth, cross-modal analysis provides compelling evidence for the transcriptomic, epigenomic and gene regulatory basis of neuronal phenotypes such as their physiological and anatomical properties, demonstrating the biological validity and genomic underpinning of neuron types. We further present an extensive genetic toolset for targeting glutamatergic neuron types towards linking their molecular and developmental identity to their circuit function. Together, our results establish a unifying and mechanistic framework of neuronal cell-type organization that integrates multi-layered molecular genetic and spatial information with multi-faceted phenotypic properties.
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- He, ZC, et al.
(författare)
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Composition of Urine Collected from Non-Stone-Forming Chinese Persons during Different Short-Term Periods of the Day
- 2022
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Ingår i: Urologia internationalis. - : S. Karger AG. - 1423-0399 .- 0042-1138. ; 106:3, s. 227-234
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Tidskriftsartikel (refereegranskat)abstract
- The purpose of this study in a small group of non-stone-forming Chinese persons was to measure the levels of supersaturation with calcium oxalate and calcium phosphate and pH with the aim of confirming if any of the different short-term urine samples were better for risk evaluation than a 24-h sample. Nine normal men and 1 woman collected urine during 4 periods of the day. <i>Period 1</i> between 08 and 12 h, <i>Period 2</i> between 12 and 18 h, <i>Period 3</i> between 18 and 22 h, and <i>Period 4</i> between 22 and 08 h. Each sample was analysed for calcium, oxalate, citrate, magnesium and phosphate, and estimates of supersaturation with calcium oxalate (CaOx) and calcium phosphate (CaP) were expressed in terms of AP(CaOx) and AP(CaP) index. An estimate of the solute load of CaOx was also calculated. Urine composition for 24-h urine (<i>Period 24</i>) was obtained mathematically from the analysed variables. Urine composition corresponding to 14-h urine portions 22–12 h (<i>Period 14</i>N) and 08–22 h (<i>Period 14 D</i>) were calculated. The lowest pH levels were recorded in <i>Period 1</i> urine. The highest level of AP(CaOx) index was recorded during <i>Period 1</i>, and the product AP(CaOx) index × 10<sup>7</sup> × hydrogen ion concentration was significantly higher in Period 1 urine than in 24-h urine (<i>p</i> = 0.02). Also, the product SL(CaOx) × 10<sup>7</sup> × hydrogen ion concentration was significantly higher in <i>Period 1</i> urine (<i>p</i> = 0.02). Low AP (CaP) index levels were recorded in <i>Period 4</i>, but also in all periods following dietary loads of calcium and phosphate. With the important reservation that the analytical results were obtained from non-stone-forming persons, the conclusion is that analysis of urine samples collected between 08 and 12 h might be an alternative to 24-h urine. The risk evaluation might advantageously be expressed either in terms of the product AP(CaOx) index × 10<sup>7</sup> × hydrogen ion concentration or the product SL(CaOx) × 10<sup>7</sup> × hydrogen ion concentration.
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