4.8 Article

Real-time, multidimensional in vivo imaging used to investigate blood flow in mouse pancreatic islets

期刊

JOURNAL OF CLINICAL INVESTIGATION
卷 118, 期 11, 页码 3790-3797

出版社

AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/JCI36209

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资金

  1. NCI NIH HHS [CA68485, P30 CA068485] Funding Source: Medline
  2. NCRR NIH HHS [S10 RR022620, RR22620] Funding Source: Medline
  3. NEI NIH HHS [P30 EY008126, EY08126] Funding Source: Medline
  4. NICHD NIH HHS [HD15052, P30 HD015052] Funding Source: Medline
  5. NIDDK NIH HHS [T32 DK007563, DK20593, R33 DK066636, DK66636, DK63439, R21 DK066636, DK68764, R21 DK063439, U24 DK059637, DK07563, P30 DK058404, DK58404, DK59637, P30 DK020593, R01 DK068764, DK53434, R01 DK069603, R01 DK053434, P60 DK020593, DK69603] Funding Source: Medline

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The pancreatic islets of Langerhans are highly vascularized micro-organs that play a key role in the regulation of blood glucose homeostasis. The specific arrangement of endocrine cell types in islets suggests a coupling between morphology and function within the islet. Here, we established a line-scanning confocal microscopy approach to examine the relationship between blood flow and islet cell type arrangement by real-time in vivo imaging of intra-islet blood flow in mice. These data were used to reconstruct the in vivo 3D architecture of the islet and time-resolved blood flow patterns throughout the islet vascular bed. The results revealed 2 predominant blood flow patterns in mouse islets: inner-to-outer, in which blood perfuses the core of beta cells before the islet perimeter of non-beta cells, and top-to-bottom, in which blood perfuses the islet from one side to the other regardless of cell type. Our approach included both millisecond temporal resolution and submicron spatial resolution, allowing for real-time imaging of islet blood flow within the living mouse, which has not to our knowledge been attainable by other methods.

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