PMID- 29215706 OWN - NLM STAT- MEDLINE DCOM- 20190415 LR - 20190415 IS - 1097-4652 (Electronic) IS - 0021-9541 (Linking) VI - 233 IP - 6 DP - 2018 Jun TI - Map and correlate intracellular calcium response and matrix deposition in cartilage under physiological oxygen tensions. PG - 4949-4960 LID - 10.1002/jcp.26326 [doi] AB - Face to the limited repair capability of cartilage, we intended to find out signaling responsible for its matrix synthesis. Since spontaneous calcium response likes a label of cell status, here it was mapped in fresh and 24 hr cultured in situ chondrocytes under oxygen tensions of 20%, 5%, and 1% as well as mimic hypoxia conditions. The calcium source was traced using ethylene glycol-bis (beta-aminoethyl ether)-N,N,N',N'-tetraacetic acid (EGTA) and thapsigargin (TG) to treat cartilage. Their relative matrix of type II collagen (COLL-II) and glycosaminoglycan (GAG) were quantified after cultured for 3 and 7 days. We disclosed the specific fingerprint of calcium response and matrix deposition along the histological zones under various oxygen tensions, from which the effects of hyperoxia, normoxia, and hypoxia conditions on as well as the optimal oxygen tensions for maintenance of various zones of cartilage or chondrocytes were derived and obtained. Our results revealed that cytoplasm calcium was conducive to synthesize COLL-II but detrimental to synthesize GAG. These results provide correlation in addition to details of intracellular calcium response and matrix deposition in in situ cartilage along its histological zones under physiological oxygen tensions. CI - (c) 2017 Wiley Periodicals, Inc. FAU - Zhou, Jin AU - Zhou J AD - Key Laboratory for Biorheological Science and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, College of Bioengineering, Chongqing University, Chongqing, China. FAU - Yue, Danyang AU - Yue D AD - Key Laboratory for Biorheological Science and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, College of Bioengineering, Chongqing University, Chongqing, China. FAU - Bai, Yuying AU - Bai Y AD - Key Laboratory for Biorheological Science and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, College of Bioengineering, Chongqing University, Chongqing, China. FAU - Kong, Fei AU - Kong F AD - Key Laboratory for Biorheological Science and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, College of Bioengineering, Chongqing University, Chongqing, China. FAU - Pan, Jun AU - Pan J AUID- ORCID: 0000-0002-5091-982X AD - Key Laboratory for Biorheological Science and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, College of Bioengineering, Chongqing University, Chongqing, China. LA - eng PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20180104 PL - United States TA - J Cell Physiol JT - Journal of cellular physiology JID - 0050222 RN - 0 (Collagen Type II) RN - 0 (Glycosaminoglycans) RN - S88TT14065 (Oxygen) RN - SY7Q814VUP (Calcium) SB - IM MH - Animals MH - Calcium/*metabolism MH - Cartilage, Articular/*metabolism/pathology MH - Cell Hypoxia MH - *Cellular Microenvironment MH - Chondrocytes/*metabolism/pathology MH - *Chondrogenesis MH - Collagen Type II/metabolism MH - Extracellular Matrix/*metabolism/pathology MH - Glycosaminoglycans/metabolism MH - Oxygen/*metabolism MH - Signal Transduction MH - Sus scrofa MH - Time Factors OTO - NOTNLM OT - GAG OT - collage-II OT - histological zone OT - hyperoxia OT - hypoxia EDAT- 2017/12/08 06:00 MHDA- 2019/04/16 06:00 CRDT- 2017/12/08 06:00 PHST- 2017/09/27 00:00 [received] PHST- 2017/11/29 00:00 [accepted] PHST- 2017/12/08 06:00 [pubmed] PHST- 2019/04/16 06:00 [medline] PHST- 2017/12/08 06:00 [entrez] AID - 10.1002/jcp.26326 [doi] PST - ppublish SO - J Cell Physiol. 2018 Jun;233(6):4949-4960. doi: 10.1002/jcp.26326. Epub 2018 Jan 4.