Cell shape alteration during adipogenesis is associated with coordinated matrix cues. Issue 4 (7th September 2018)
- Record Type:
- Journal Article
- Title:
- Cell shape alteration during adipogenesis is associated with coordinated matrix cues. Issue 4 (7th September 2018)
- Main Title:
- Cell shape alteration during adipogenesis is associated with coordinated matrix cues
- Authors:
- Mor‐Yossef Moldovan, Lisa
Lustig, Maayan
Naftaly, Alex
Mardamshina, Mariya
Geiger, Tamar
Gefen, Amit
Benayahu, Dafna - Abstract:
- Abstract: Obesity has become one of the leading pathophysiologic disorders in recent years. Adipose tissue is the main tissue related to obesity and is known to play a role in various physiological complications, including type 2 diabetes. To better understand how the fat tissue develops, we used an in vitro live cell imaging system to quantify the adipogenesis by means of nondestructive digital imaging to monitor the accumulation of intracellular lipid droplets (LDs), a hallmark of adipogenesis, from the macro‐ to the micro‐scale. Analyzing the cells' shape at the single‐cell level allows to quantify the cells' shape change from a fibroblast to spherical morphology, indicating the start of adipogenesis. To reveal the molecular alterations, we applied a proteomic approach using high‐resolution mass spectrometry of the proliferation, confluent fibroblasts and of adipocytes. During this process, we noted the reorganization of the cells' extracellular matrix (ECM) network microenvironment from fibrillary collagen types I, III and V to collagens IV and VI, which affected the cells niche. The changes in ECM are translated for cytoskeleton remodeling according to cell fate‐determining mechanisms. We quantified the cytoskeleton rearrangement of long oriented actin fibers or short cortical and disorganized fibers, associated with LDs accumulation in adipocytes. Developing in vitro models and analytical methods enable us to study differentiation into adipocytes that will advance ourAbstract: Obesity has become one of the leading pathophysiologic disorders in recent years. Adipose tissue is the main tissue related to obesity and is known to play a role in various physiological complications, including type 2 diabetes. To better understand how the fat tissue develops, we used an in vitro live cell imaging system to quantify the adipogenesis by means of nondestructive digital imaging to monitor the accumulation of intracellular lipid droplets (LDs), a hallmark of adipogenesis, from the macro‐ to the micro‐scale. Analyzing the cells' shape at the single‐cell level allows to quantify the cells' shape change from a fibroblast to spherical morphology, indicating the start of adipogenesis. To reveal the molecular alterations, we applied a proteomic approach using high‐resolution mass spectrometry of the proliferation, confluent fibroblasts and of adipocytes. During this process, we noted the reorganization of the cells' extracellular matrix (ECM) network microenvironment from fibrillary collagen types I, III and V to collagens IV and VI, which affected the cells niche. The changes in ECM are translated for cytoskeleton remodeling according to cell fate‐determining mechanisms. We quantified the cytoskeleton rearrangement of long oriented actin fibers or short cortical and disorganized fibers, associated with LDs accumulation in adipocytes. Developing in vitro models and analytical methods enable us to study differentiation into adipocytes that will advance our understanding regarding the niche conditions that affect adipogenesis. Consequently, this will enable the development of new modalities to prevent obesity and its deleterious outcomes and to develop potential treatments to battle pathophysiology‐related diseases. Abstract : Schematic illustration of differentiation from an elongated fibroblast to a round mature adipocyte that accumulates lipid droplets (LDs). The proteomic approach allows identifying the reorganization of the cells' extracellular matrix (ECM) microenvironment associated with cytoskeleton remodeling according to cell fate. … (more)
- Is Part Of:
- Journal of cellular physiology. Volume 234:Issue 4(2019:Apr.)
- Journal:
- Journal of cellular physiology
- Issue:
- Volume 234:Issue 4(2019:Apr.)
- Issue Display:
- Volume 234, Issue 4 (2019)
- Year:
- 2019
- Volume:
- 234
- Issue:
- 4
- Issue Sort Value:
- 2019-0234-0004-0000
- Page Start:
- 3850
- Page End:
- 3863
- Publication Date:
- 2018-09-07
- Subjects:
- adipogenesis -- cell niche -- collagens -- ECM and cytoskeleton remodeling -- mass spectrometry
Physiology -- Periodicals
Cell physiology -- Periodicals
571.6 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4652 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jcp.27157 ↗
- Languages:
- English
- ISSNs:
- 0021-9541
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4955.020000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 26353.xml