High-resolution magnetic resonance histology of the embryonic and neonatal mouse: A 4D atlas and morphologic database

被引:86
作者
Petiet, Alexandra E. [1 ,3 ]
Kaufman, Matthew H. [4 ]
Goddeeris, Matthew M. [6 ]
Brandenburg, Jeffrey [1 ]
Elmore, Susan A. [5 ]
Johnson, G. Allan [1 ,2 ,3 ]
机构
[1] Duke Univ, Med Ctr, Ctr In Vivo Microscopy, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Radiol, Durham, NC 27710 USA
[3] Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA
[4] Univ Edinburgh, Dept Biomed Sci, Edinburgh EH8 9XD, Midlothian, Scotland
[5] NIEHS, Lab Expt Pathol, Res Triangle Pk, NC 27709 USA
[6] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
基金
美国国家卫生研究院;
关键词
digital atlas; magnetic resonance microscopy; mouse embryo;
D O I
10.1073/pnas.0805747105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Engineered mice play an ever-increasing role in defining connections between genotype and phenotypic expression. The potential of magnetic resonance microscopy (MRM) for morphologic phenotyping in the mouse has previously been demonstrated; however, applications have been limited by long scan times, availability of the technology, and a foundation of normative data. This article describes an integrated environment for high-resolution study of normal, transgenic, and mutant mouse models at embryonic and neonatal stages. Three-dimensional images are shown at an isotropic resolution of 19.5 mu m (voxel volumes of 8 pL), acquired in 3 h at embryonic days 10.5-19.5 (10 stages) and postnatal days 0-32 (6 stages). A web-accessible atlas encompassing this data was developed, and for critical stages of embryonic development (prenatal days 14.5-18.5), > 200 anatomical structures have been identified and labeled. Also, matching optical histology and analysis tools are provided to compare multiple specimens at multiple developmental stages. The utility of the approach is demonstrated in characterizing cardiac septal defects in conditional mutant embryos lacking the Smoothened receptor gene. Finally, a collaborative paradigm is presented that allows sharing of data across the scientific community. This work makes magnetic resonance microscopy of the mouse embryo and neonate broadly available with carefully annotated normative data and an extensive environment for collaborations.
引用
收藏
页码:12331 / 12336
页数:6
相关论文
共 31 条
[1]   NUCLEAR-MAGNETIC-RESONANCE IMAGING OF A SINGLE CELL [J].
AGUAYO, JB ;
BLACKBAND, SJ ;
SCHOENIGER, J ;
MATTINGLY, MA ;
HINTERMANN, M .
NATURE, 1986, 322 (6075) :190-191
[2]   Multiple-mouse MRI [J].
Bock, NA ;
Konyer, NB ;
Henkelman, RM .
MAGNETIC RESONANCE IN MEDICINE, 2003, 49 (01) :158-167
[3]  
Callaghan P.T., 1991, Principles of nuclear magnetic resonance microscopy, V1st
[4]   Three-dimensional digital mouse atlas using high-resolution MRI [J].
Dhenain, M ;
Ruffins, SW ;
Jacobs, RE .
DEVELOPMENTAL BIOLOGY, 2001, 232 (02) :458-470
[5]   HIGH-RESOLUTION IMAGING - THE NMR MICROSCOPE [J].
ECCLES, CD ;
CALLAGHAN, PT .
JOURNAL OF MAGNETIC RESONANCE, 1986, 68 (02) :393-398
[6]   MAGNETIC-RESONANCE MICROSCOPY OF CHICK-EMBRYOS IN OVO [J].
EFFMANN, EL ;
JOHNSON, GA ;
SMITH, BR ;
TALBOTT, GA ;
COFER, G .
TERATOLOGY, 1988, 38 (01) :59-65
[7]   Independent requirements for Hedgehog signaling by both the anterior heart field and neural crest cells for outflow tract development [J].
Goddeeris, Matthew M. ;
Schwartz, Robert ;
Klingensmith, John ;
Meyers, Erik N. .
DEVELOPMENT, 2007, 134 (08) :1593-1604
[8]   Alteration in connexin 43 gap junction gene dosage impairs conotruncal heart development [J].
Huang, GY ;
Wessels, A ;
Smith, BR ;
Linask, KK ;
Ewart, JL ;
Lo, CW .
DEVELOPMENTAL BIOLOGY, 1998, 198 (01) :32-44
[9]   Towards a microMRI atlas of mouse development [J].
Jacobs, RE ;
Ahrens, ET ;
Dickinson, ME ;
Laidlaw, D .
COMPUTERIZED MEDICAL IMAGING AND GRAPHICS, 1999, 23 (01) :15-24
[10]   Morphologic phenotyping with MR microscopy: The visible mouse [J].
Johnson, GA ;
Cofer, GP ;
Gewalt, SL ;
Hedlund, LW .
RADIOLOGY, 2002, 222 (03) :789-793